 HERBICIDAL COMPOSITIONS UNDERSTANDING 4-AMINO-3-CHLORINE-5-FLUORINE-6 (4-CHLORINE-2-FLUORO-3-METOXYP
专利摘要:
HERBICIDAL COMPOSITIONS UNDERSTANDING 4-AMINO-3-CHLORINE-5-FLUORO-6- (4-CHLORINE-2- FLUORO-3-METHOD-XYphenyl) ACID PYRIDINE-2-CARBOXYLIC OR A DERIVATIVE OF THIS AND ACETYL-COA CARBOXILATE INHIBITORS ACCASE). The present invention relates to synergistic herbicidal compositions and methods that contain / use (a) a compound of formula (I), 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro) -3-methoxy-phenyl) pyridine-2-carboxylic or an agriculturally acceptable salt or ester thereof and (b) an ACCase inhibitor, including, for example, cletodim, clodinafop-propargyl, cyhalofop-R-butyl, diclofop-methyl, fenoxaprop-P-ethyl, fluazifop-P-butyl, haloxifop-R-methyl, metamifop, pinoxaden, profoxidim, quizalofop-P-ethyl, setoxidim and tralcoxidim, provide synergistic control of weeds from undesirable vegetation in rice, cereals, wheat, barley, oats, rye, sorghum, corn, sugar cane, sunflower, rapeseed, canola, beet, soy, cotton, pineapple, pastures, lawns, pastures, abandoned land, grass, trees and grape orchards, aquatic, crops planting, vegetables, industrial vegetation management (IVM) or rights of way (ROW). 公开号:BR102013018472B1 申请号:R102013018472-1 申请日:2013-07-19 公开日:2020-11-17 发明作者:Carla Yerkes；Norbert Satchivi；Richard Mann；Monte Weimer；Nelson Carranza 申请人:Dow Agrosciences Llc； IPC主号:
专利说明:
Priority Claim [0001] This application claims the benefit of provisional patent application US 61 / 675,103, filed on July 24, 2012, and patent application of US 13 / 839,043, filed on March 15, 2013, the disclosure of which is each incorporated herein by reference in its entirety. Field [0002] Herbicidal compositions are provided here comprising (a) 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or an ester or agriculturally acceptable salt of this and (b) an acetyl-CoA carboxylase inhibitor (ACCase) and methods of controlling undesirable vegetation using them. Background [0003] The protection of crops from weeds and other vegetation that inhibit crop growth is a constantly recurring problem in agriculture. To help combat this problem, researchers in the field of synthetic chemistry have produced an extensive variety of chemicals and chemical formulations that are effective in controlling such unwanted growth. Chemical herbicides of many types have been reported in the literature and a large number are in commercial use. However, there remains a need for compositions and methods that are effective in controlling undesirable vegetation. summary [0004] A first embodiment includes herbicidal compositions comprising: a herbicidally effective amount of (a) a compound of Formula (I) or an agriculturally acceptable salt or ester thereof, and (b) ACCase inhibitors, or a salt or ester thereof. [0005] A second embodiment includes a composition according to the first embodiment, wherein (a) is a C1-4 alkyl or benzyl ester of compound (I). [0006] A third embodiment includes a composition according to the first embodiment, wherein (a) is a benzyl ester of compound (I). [0007] A fourth embodiment includes a composition according to the first embodiment, wherein (a) is the compound of Formula (I), which is carboxylic acid. [0008] A fifth modality includes compositions of the first, second, third or fourth modality, in which (b) is selected from the group consisting of: clethodim, clodinafop-propargyl, cyhalofop-P-butyl, diclofop-methyl, phenoxaprop-P- ethyl, fluazifop-P-butyl, haloxifop-P-methyl, metamifop, pinoxaden, profoxidim, quizalofop-P-ethyl, setoxidim or tralcoxidim. [0009] A sixth embodiment includes a composition of the first embodiment, in which (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is clethodim. [00010] A seventh embodiment includes a composition of the first embodiment, in which (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is clodinafop-propargyl. [00011] An eighth embodiment includes a composition of the first embodiment, in which (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is cyhalofop-R-butyl. [00012] A ninth embodiment includes a composition of the first embodiment, in which (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is diclofop-methyl. [00013] A tenth embodiment includes a composition of the first embodiment, in which (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is phenoxaprop-P-ethyl. [00014] An eleventh embodiment includes a composition of the first embodiment, in which (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is fluazifop-P-butyl. [00015] A twelfth embodiment includes a composition of the first embodiment, in which (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is haloxifop-R-methyl. [00016] A thirteenth embodiment includes a composition of the first embodiment, in which (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is metamifop. [00017] A fourteenth embodiment includes a composition of the first embodiment, in which (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is pinoxaden. [00018] A fifteenth embodiment includes a composition of the first embodiment, in which (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is profoxidim. [00019] A sixteenth modality includes a composition of the first modality, in which (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is quizalofop-P-ethyl. [00020] A seventeenth embodiment includes a composition of the first embodiment, in which (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) setoxidim. [00021] An eighteenth modality includes a composition of the first modality, in which (a) is the compound of Formula (I) or an agriculturally acceptable benzyl ester and (b) is tralquioxidim. [00022] A nineteenth modality includes the composition according to the first through the eighteenth modality which further comprises a herbicide protector. [00023] A twentieth modality includes a composition according to the first modality, in which the ratios of the compound of Formula (I) or its agriculturally acceptable salt or ester to clethodim or an agriculturally acceptable salt or ester thereof, expressed in units of weight for weight (g to g), g ea / ha to g ia / ha, or g ea / ha to g ea / ha, are within the range of about 1: 140 to about 9: 1, about 1 : 35 to about 2.2: 1 and about 1: 9 to about 1: 8. [00024] A twenty-first embodiment includes a composition according to the first embodiment, in which the ratios of the compound of Formula (I) or its agriculturally acceptable salt or ester to clodinafop-propargyl or an agriculturally acceptable salt or ester thereof, expressed in units of weight for weight (g to g), g ea / ha to g ia / ha, or g ea / ha to g ea / ha, are within the range of about 1:40 to about 60: 1 from about 1/6 to about 2: 3 and from about 1: 3 to about 1: 4. [00025] A twenty-second embodiment includes a composition according to the first embodiment, wherein the ratios of the compound of Formula (I) or its agriculturally acceptable salt or ester to cyclic-R-butyl or an agriculturally acceptable salt or ester of this, expressed in units of weight for weight (g to g), g ea / ha to g ia / ha, or g ea / ha to g ea / ha, are within the range of about 1: 155 to about 6 : 1, from about 1:34 to about 1: 2, from about 1:10 to about 1:70, 4: 1, 0.5: 1, 1:07 and about 1: 9. [00026] A twenty-third modality includes a composition according to the first modality, in which the ratios of the compound of Formula (I) or its agriculturally acceptable salt or ester to diclofop-methyl or an agriculturally acceptable salt or ester thereof, expressed in units of weight for weight (g to g), g ea / ha to g ia / ha, or g ea / ha to g ea / ha, are within the range of about 1: 560 to about 5: 1 , from about 1: 140 to 1: 9 and 1:35. [00027] A twenty-fourth modality includes a composition according to the first modality, in which the ratios of the compound of Formula (I) or its agriculturally acceptable salt or ester to phenoxaprop-P-ethyl or an agriculturally acceptable salt or ester thereof, expressed in units of weight for weight (g to g), g ea / ha to g ia / ha, or g ea / ha to g ea / ha, are within the range of about 1: 170 to about 30: 1 , from about 1:16 to about 4: 1, from about 0.4: 1 to about 0.6: 1, 0.25: 1 and 0.6: 1 and isoxadiphenyl methyl culture protectors and mefempir-diethyl are incorporated into the product. [00028] A twenty-fifth embodiment includes a composition according to the first embodiment, wherein the ratios of the compound of Formula (I) or its agriculturally acceptable salt or ester to fluazifop-P-butyl or an agriculturally acceptable salt or ester of this, expressed in units of weight for weight (g to g), g ea / ha to g ia / ha, or g ea / ha to g ea / ha, are within the range of about 1: 210 to about 3 : 1, from about 1:41 to 0.8: 1 and from 1:10 to about 1: 5. [00029] A twenty-sixth modality includes a composition according to the first modality, wherein the ratios of the compound of Formula (I) or its agriculturally acceptable salt or ester to haloxifop-P-methyl or an agriculturally acceptable salt or ester of this, expressed in units of weight for weight (g to g), g ea / ha to g ia / ha, or g ea / ha to g ea / ha, are within the range of about 1:45 to about 10: 1, from about 1: 6 to about 1: 5, from about 0.65: 1 and about 1.3: 1. [00030] A twenty-seventh modality includes a composition according to the first modality, in which the ratios of the compound of Formula (I) or its agriculturally acceptable salt or ester to metatifop or an agriculturally acceptable salt or ester thereof, expressed in weight to weight units (g to g), g ea / ha to g ia / ha, or g ea / ha to g ea / ha, are within the range of about 1: 150 to about 6: 1, about 1:34 to about 10: 1, about 1: 2 to about 0.64: 1, 0.6: 1, 1: 1, 1: 4 and 3: 1. [00031] A twenty-eighth modality includes a composition according to the first modality, in which the ratios of the compound of Formula (I) or its agriculturally acceptable salt or ester to pinxaden or an agriculturally acceptable salt or ester thereof, expressed in weight to weight units (g to g), g ea / ha to g ia / ha, or g ea / ha to g ea / ha, are within the range of about 1:30 to about 150: 1, about 1:12 to about 2: 1, about 1: 3 to about 1: 2, 2: 1 and 1: 2. [00032] A twenty-ninth modality includes a composition according to the first modality, in which the ratios of the compound of Formula (I) or its agriculturally acceptable salt or ester to pro- foxidim or an agriculturally acceptable salt or ester thereof, expressed in Weight to weight units (g to g), g ea / ha to g ia / ha, or g ea / ha to g ea / ha, are within the range of about 1:70 to about 29: 1, from about 1:23 to about 3: 1, about 3: 1 to about 1: 3, 0.35: 1, 0.17: 1, 2.8: 1 and 1.4: 1. [00033] A thirtieth modality includes a composition according to the first modality, wherein the ratios of the compound of Formula (I) or its agriculturally acceptable salt or ester of quizalofop-P-ethyl or an agriculturally acceptable salt or ester thereof, expressed HX72 in units of weight to weight (gag), g ea / ha to g ia / ha, or g ea / ha to g ea / ha, are within the range of about 1: 100 to about 12: 1, from about 1: 8 to about 19: 1, 5: 1, 1.16: 1, 0.6: 1, 9: 1, 2.33: 1 and 1.2: 1. [00034] A thirty-first embodiment includes a composition according to the first embodiment, in which the ratios of the compound of Formula (I) or its agriculturally acceptable salt or ester to sexy toxin or an agriculturally acceptable salt or ester thereof, expressed in Weight to weight units (g to g), g ea / ha to g ia / ha, or g ea / ha to g ea / ha, are within the range of about 1:70 to about 29: 1, from about 1:62 to about 0.6: 1, about 13: 1 to about 1: 8.5, 1: 7.7, 1: 30.9, 0.5: 1 and 1: 8 , 5. [00035] A thirty-second embodiment includes a composition according to the first embodiment, in which the ratios of the compound of Formula (I) or its agriculturally acceptable salt or ester to tralcoxidim or an agriculturally acceptable salt or ester thereof, expressed as Weight to weight units (g to g), g ea / ha to g ia / ha, or g ea / ha to g ea / ha, are within the range of about 1:38 to about 60: 1, from about 1:40 to about 0.6: 1, about 1:10 to about 1: 6.3, 1: 3, 1: 6 and 1: 1.5. [00036] A thirty-third modality includes any composition according to the first to the thirty-second modality which further comprises an agriculturally acceptable adjuvant and / or vehicle, and / or herbicide protector. [00037] A thirty-fourth modality includes any composition according to the first to the thirty-third modality, in which the synergy between the herbicides is determined by the Colby equation. [00038] A thirty-fifth embodiment includes any composition according to the first embodiment, in which (b) is cyhalofop-butyl or carboxylic acid, carboxylate salt, or an ester thereof, in which the composition further comprises penoxsulam, bentazon-sodium , triclopir, bispiribac-sodium, imazamox, benzobicyclon, quinclorac, glyphosate, glufosinate, benfuresate, fentrazamide, indanofan, ipfencarbazone, mefena-cet, oxaziclomefone, pretilachlor, propyrsulfuron, pyraclonimide, pyraclonimide, pyraclonil, pyraclonil, pyraclonil, salty carboxylate, or agriculturally acceptable ester thereof, in combination as a 3-way / ternary synergistic mixture. [00039] A thirty-sixth modality includes any composition according to the first modality, in which (b) is phenoxaprop, metamifop, or profoxidim, or an agriculturally acceptable salt, ester, carboxylate salt, or carboxylic acid thereof, wherein the The composition further comprises penoxsulam, bentazon-sodium, triclopyr, bispyribac-sodium, imazamox, benzobicyclon, quinclorac, glyphosate, glufosinate, benfuresate, fentrazamide, indanofan, ipfencarbazone, mefenacet, oxaziclomefone, piranilone, pirilacidone, pirilacidone, pirilacidone , carboxylic acid, carboxylate salt or agriculturally acceptable ester thereof, in combination as a 3-way / ternary synergistic mixture. [00040] A thirty-seventh modality includes methods for the control of undesirable vegetation that comprises the stages of contact of the vegetation or its location with the soil or water to prevent the appearance or growth of vegetation of at least one composition according to first to the thirty-sixth modality. [00041] A thirty-eighth modality includes methods for the control of undesirable vegetation which comprises the stages of contact of vegetation or its location with soil or water to prevent the appearance or growth of vegetation using a herbicidally effective amount of (a ) a compound of Formula (I) or an agriculturally acceptable salt or ester thereof, and (b) an ACCase inhibitor. [00042] The thirty-ninth modality includes methods of the thirty-seventh and thirty-eighth modalities, in which undesirable vegetation is controlled in rice, cereals, wheat, barley, oats, rye, sorghum, corn, sugar cane, sunflower, rapeseed, canola, beet, soy, cotton, pineapple, pastures, lawns, pastures, abandoned land, grass, trees and grape orchards, aquatic, plantation crops, industrial vegetation management (IVM) or easements (ROW). [00043] The fortieth modality in which undesirable vegetation is immature. [00044] The forty-first modality includes methods of the thirty-seventh and the thirty-eighth modalities in which compounds (a) and (b) are applied in water. [00045] The forty-second modality includes methods according to the forty-first modality, in which the water is part of a flooded rice field. [00046] The forty-third modality includes methods according to the thirty-seventh and thirty-eighth modalities, in which compounds (a) and (b) are applied pre-emergence to weed or crop. [00047] The forty-fourth modality includes methods according to the thirty-seventh and thirty-eighth modalities, in which compounds (a) and (b) are applied post-emergence to weed or crop. [00048] The forty-fifth modality includes methods according to the thirty-seventh and thirty-eighth modalities, in which undesirable vegetation is controlled with glyphosate-tolerant crops, inhibitor of 5-enolpyruvylchiquime-3-phosphate (EPSP), glu - phosinate, glutamine synthetase inhibitor, dicamba, phenoxy auxin, pyridyloxy, synthetic auxin, auxin transport inhibitor, aryloxyphenoxypropionate, cyclohexanedione, phenylpyrazoline, acetyl CoA carboxylase inhibitor (ACCase), imidazolinone, pyridylamine ato, triazolopyrimidine, sulfonylaminocarbonyltriazolinone, acetolactate synthase (ALS) or acetohydroxy acid (AH-AS) synthase inhibitor, 4-hydroxyphenyl-pyruvate dioxigenase (HPPD) inhibitor, phytene desaturase inhibitor, biosynthesis inhibitor, biosynthesis inhibitor protoporphyrinogen oxidase (PPO) inhibitor, cellulose biosynthesis inhibitor, mitosis inhibitor, microtubule inhibitor, fatty acid inhibitor very long chain, inhibitor of fatty acid and lipid biosynthesis, inhibitor of photosystem I, inhibitor of photosystem II, triazine, or bromoxynil. [00049] The forty-sixth modality includes methods according to the forty-fifth modality, in which the resistant or tolerant culture has multiple or concentrated traits that confer resistance or tolerance to several herbicides or several modes of action. [00050] The forty-seventh modality includes methods according to the thirty-seventh and thirty-eighth modalities, in which the undesirable vegetation comprises a herbicide-resistant or tolerant weed. [00051] The forty-eighth modality includes methods according to the forty-seventh modality, in which the resistant or tolerant weed is a biotype with resistance or tolerance to multiple herbicides, multiple chemical classes or multiple modes of action of the herbicide, or through multiple resistance mechanisms. [00052] The forty-ninth modality includes methods according to the forty-seventh modality in which the resistant or tolerant weed is a biotype resistant or tolerant to acetolactate synthase (ALS) or acetohydroxy acid synthase (AHAS) inhibitors. , photosystem II inhibitors, acetyl CoA carboxylase (ACCase) inhibitors, synthetic auxins, auxin transport inhibitors, photosystem I inhibitors, 5-enolpyruvylchiquimato-3-phosphate (EPSP) synthase inhibitors, microtubule assembly inhibitors, fatty acid and lipid synthesis inhibitors, protoporphyrinogen oxidase (PPG) inhibitors, carotenoid biosynthesis inhibitors, very long chain fatty acid inhibitors (VLCFA), phytene desaturase (PDS) inhibitors, glu synthase inhibitors - tamine, 4-hydroxyphenyl-pyruvate-dioxigenase (HPPD) inhibitors, mitosis inhibitors, cellulose biosynthesis inhibitors, herbicides with multiple modes of action, quinclorac, acid arylaminopropionic, diphenzoquat, endotal, or organoarsenic acids. [00053] The fiftieth modality includes the composition according to any of the modalities 1 to 4, in which the ratio of compound (a) to compound (b) is such that the composition presents synergy. [00054] The fifty-first modality includes the composition according to any one of the modalities 1 to 4 or 50, wherein the weight ratio of the compound of Formula (I) or its agriculturally acceptable salt or ester to clethodim or its salt or agriculturally acceptable ester is about 1: 140 to about 9: 1. [00055] The fifty-second modality includes the composition according to any one of the modalities 1 to 4 or 50, wherein the weight ratio of the compound of Formula (I) or its agriculturally acceptable salt or ester to clodinafop-propargyl or its agriculturally acceptable salt or ester is about 1:40 to about 60: 1. [00056] The fifty-third modality includes the composition according to any of the modalities 1 to 4 or 50, wherein the weight ratio of the compound of Formula (I) or its agriculturally acceptable salt or ester to cyhalofop-R-butyl or its agriculturally acceptable salt or ester is about 1: 155 to about 6: 1. [00057] The fifty-fourth modality includes the composition according to any one of the modalities 1-4 or 50, wherein the weight ratio of the compound of Formula (I) or its agriculturally acceptable salt or ester to diclofop-methyl or its agriculturally acceptable salt or ester is about 1: 560 to about 5: 1. [00058] The fifty-fifth modality includes the composition according to any one of modalities 1 to 4 or 50, wherein the weight ratio of the compound of Formula (I) or its agriculturally acceptable salt or ester to phenoxaprop-P-ethyl or its agriculturally acceptable salt or ester is from about 1: 170 to about 30: 1, and the culture protectors isoxadifen-methyl and mefenpir-diethyl are incorporated into the product. [00059] The fifty-sixth modality includes the composition according to any of the modalities 1 to 4 or 50, wherein the weight ratio of the compound of Formula (I) or its agriculturally acceptable salt or ester to fluazifop-P-butyl or its agriculturally acceptable salt or ester is from about 1: 210 to about 3: 1. [00060] The fifty-seventh modality includes the composition according to any one of modalities 1 to 4 or 50, wherein the weight ratio of the compound of Formula (I) or its agriculturally acceptable salt or ester to haloxifop-P-methyl or its agriculturally acceptable salt or ester is about 1:45 to about 10: 1. [00061] The fifty-eighth modality includes the composition according to any one of the modalities 1 to 4 or 50, wherein the weight ratio of the compound of Formula (I) or its agriculturally acceptable salt or ester to metamifop or its salt or agriculturally acceptable ester is about 1: 150 to about 6: 1. [00062] The fifty-ninth modality includes the composition according to any one of the modalities 1 to 4 or 50, wherein the weight ratio of the compound of Formula (I) or its agriculturally acceptable salt or ester to pinoxaden or its salt or agriculturally acceptable ester is about 1:30 to about 150: 1. [00063] The sixtieth modality includes the composition according to any one of the modalities 1 to 4 or 50, wherein the weight ratio of the compound of Formula (I) or its agriculturally acceptable salt or ester to profoxidim or its salt or ester agriculturally acceptable is about 1:70 to about 29: 1. [00064] The sixty-first modality includes the composition according to any of the modalities 1 to 4 or 50, in which the weight ratio of the compound of Formula (I) or its agriculturally acceptable salt or ester to quizalofop-P-ethyl or its agriculturally acceptable salt or ester is about 1: 100 to about 12: 1. [00065] The sixty-second modality includes the composition according to any one of the modalities 1 to 4 or 50, wherein the weight ratio of the compound of Formula (I) or its agriculturally acceptable salt or ester to setoxidim or its salt or agriculturally acceptable ester, is about 1:70 to about 29: 1. [00066] The sixty-third modality includes the composition according to any one of the modalities 1 to 4 or 50, wherein the weight ratio of the compound of Formula (I) or its agriculturally acceptable salt or ester to tralcoxidim or its salt or agriculturally acceptable ester, is about 1:38 to about 60: 1. [00067] Provided here are herbicidal compositions comprising a method of controlling undesirable vegetation that uses a herbicidally effective amount of (a) a compound of Formula (I) - or an agriculturally acceptable salt or ester thereof, and (b) an ACCase inhibitor. Exemplary ACCase inhibitors include, but are not limited to, cletodim, clodinafop-propargyl, cyhalofop-P-butyl, di-clofop-methyl, phenoxaprop-P-ethyl, fluazifop-P-butyl, haloxifop-P-methyl, metamifop, pinoxaden, profoxidim, quizalofop-P-ethyl, setoxidim or tralcoxidim. The compositions can also contain an agriculturally acceptable adjuvant or vehicle. Detailed Description DEFINITIONS [00068] As used herein, the compound of Formula (I) has the following structure: [00069] The compound of Formula (I) can be identified by the name 4-amino-3-chloro-6- (4-chloro-2-fluoro-3-methoxyphenyl) -5-fluoro-pyridine-2-carboxylic acid and has been described in US Patent 7,314,849 (B2), which is incorporated herein by reference in its entirety. Exemplary uses of the compound of Formula (I) include the control of undesirable vegetation, including grass weeds, broad leaves and sedge, in multiple non-cultivation and cultivation situations. [00070] Without being limited to any theory, ACCase inhibitors are believed to inhibit acetyl coenzyme A carboxylase (ACCase) to any extent, an enzyme involved in fatty acid synthesis. Exemplary ACCase inhibitors include, but are not limited to, aryloxyphenoxy propionates and cyclohexanediones. Other examples include, but are not limited to, cletodim, clodinafop-propargyl, cyhalofop-P-butyl, diclofop-methyl, phenoxaprop-P-ethyl, fluazifop-P-butyl, haloxifop-P-methyl, metamifop, pinoxaden, pro - foxidim, quizalofop-P-ethyl, setoxidim and tralcoxidim. [00071] As used herein, clethodim is 2- [1 - [[[(2E) -3-chloro-2-propen-1-yl] oxy] imino] propyl] -5- [2- (ethylthio) propyl] -3-hydroxy-2-cyclohexen-1-one and has the following structure: [00072] This compound is described in Tomlin, C., ed. A World Compendium The Pesticide Manual. 15th ed. Alton: BCPC Publications, 2009 (hereinafter “The Pesticide Manual, Fifteenth Edition, 2009.”). Exemplary uses of clethodim include its use as a herbicide for, for example, post-emergent control of annual and perennial grasses in leafy crops, vegetables, trees and vines. [00073] As used herein, clodinafop-propargyl is 2-propynyl (2R) - 2- [4 - [(5-chloro-3-fluor-2-pyridinyl) oxy] phenoxy] propanoate and has the following structure: [00074] This compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of clodinafop-propargyl include its use as an herbicide for, for example, post-emergent control of annual grasses, including, for example, Avena, Lolium, Setaria, Phalaris and Alopecurus spp., In cereals. [00075] As used herein, cyhalofop-butyl is butyl (2R) -2- [4- (4-cyano-2-fluorophenoxy) phenoxy] propanoate and has the following structure: [00076] This compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of cyhalofop-butyl include its use as an herbicide for, for example, the post-emergent control of annual and perennial weeds in seeded rice and transplanted. [00077] As used herein, diclofop-methyl is methyl 2- [4- (2,4-dichlorophenoxy) phenoxy] propanoate and has the following structure: [00078] This compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of diclofop-methyl include its use as an herbicide for, for example, post-emergent control of wild oats, wild millet, and others annual grass weeds in wheat, barley, rye, red fescue, and broadleaf crops. [00079] As used herein, phenoxaprop-P-ethyl represents ethyl (2R) - 2- [4 - [(6-chloro-2-benzoxazolyl) oxy] phenoxy] propanoate and has the following structure: [00080] This compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of phenoxaprop-P-ethyl include its use as an herbicide for, for example, the control of annual and perennial grassy weeds in crops including rice. [00081] As used herein, fluazifop-P-butyl is butyl (2R) -2- [4 - [[5- (trifluoromethyl) -2-pyridinyl] oxy] phenoxy] propanoate and has the following structure: [00082] This compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of fluazifop-P-butyl include its use as an herbicide for, for example, post-emergent control of wild oats, voluntary cereals and annual and perennial grassy weeds in rapeseed, sugar beet, fodder beet, potatoes, vegetables, cotton, soy, pommel fruit, stone fruit, shrub fruit, vines, citrus, pineapple, banana, strawberry, sunflower, alfalfa, coffee, ornamental plants and other leafy crops. Fluazifop-P-butyl can be used in combination with protectors, for example, isoxadifen-ethyl or mefenpir-diethyl. [00083] As used herein, haloxifop-P-methyl is (2R) -2- [4 - [[3-chloro-5- (trifluoromethyl) -2-pyridinyl] oxy] phenoxy] propanoate and has the following structure : [00084] This compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of haloxifop-P-methyl include its use as an herbicide for, for example, the post-emergent control of annual and perennial grasses in a variety of cultures. [00085] As used herein, metamifop is (2R) -2- [4 - [(6-chloro-2-benzoxazolyl) oxy] phenoxy] -N- (2-fluorophenyl) -N-methylpropanamide and has the following structure: [00086] This compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of metamifop include its use as an herbicide for, for example, the post-emergent control of annual and perennial grasses in a variety of crops, including rice. [00087] As used herein, pinoxaden is 8- (2,6-diethyl-4-methylphenyl) - 1,2,4,5-tetrahydro-7-oxo-7H-pyrazolo [1,2-d] [ 1,4,5] oxadiazepin-9-yl 2,2-dimethylpropanoate and has the following structure: [00088] This compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of pinoxaden include its use as a herbicide for, for example, the post-emergent control of annual grasses, including Alopecurus, Apera, Avena, Lolium, Phalaris and Setaria spp., In wheat and barley. [00089] As used herein, profoxidim is 2- [1 - [[2- (4-chlorophenoxy) propoxy] imino] butyl] -3-hydroxy-5- (tetrahydro-2H-thiopyran-3-yl) - 2-cyclohexen-1-one and has the following structure: [00090] This compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of profoxidim include its use as an herbicide for, for example, weed control in rice. [00091] As used herein, quizalofop-P-ethyl represents ethyl (2R) - 2- [4 - [(6-chloro-2-quinoxalinyl) oxy] phenoxy] propanoate and has the following structure: [00092] This compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of quizalofop-P-ethyl include its use as an herbicide for, for example, post-emergence selective control of annual grass weeds and perennials in crops. [00093] As used herein, setoxidim is 2- [1- (ethoxyimino) butyl] -5- [2- (ethylthio) propyl] -3-hydroxy-2-cyclohexen-1-one and has the following structure: [00094] This compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of setoxidim include its use as an herbicide for, for example, the control of annual and perennial grasses in leafy crops. [00095] As used herein, tralkoxydim is 2- [1- (ethoxyimino) -propyl] - 3-hydroxy-5- (2,4,6-trimethylphenyl) -2-cyclohexen-1-one and has the following structure: [00096] This compound is described in The Pesticide Manual, Fifteenth Edition, 2009. Exemplary uses of tralcoxidim include its use as an herbicide for, for example, the post-emergent control of annual grass weeds in wheat and barley. [00097] As used herein, herbicide means a compound, for example, an active ingredient that kills, controls, or otherwise adversely modifies the growth of plants. [00098] As used herein, an herbicidally effective or vegetation control amount is an amount of active ingredient that causes an adverse modification effect on the vegetation, for example, causing deviations from natural development, death, executing regulation, motivating desiccation , causing delay, and more. [00099] As used herein, undesirable vegetation control means preventing, reducing, killing, or otherwise adversely modifying the development of plants and vegetation. Methods for controlling undesirable vegetation by applying certain herbicidal combinations or compositions are described herein. Application methods include, but are not limited to, applications in the vegetation or in its location, for example, application in the area adjacent to the vegetation, as well as pre-emergence, post-emergence, leaf (dispersion, directed, associated, local, mechanical, surface or rescue) and in water applications (emerged and submerged vegetation, dispersion, local, mechanical, injected with water, granular dispersion, granular location, mixing container, or spray stream) via handheld device, backpack, machine, tractor, or aerial application methods (airplane and helicopter). [000100] As used herein, plants and vegetation include, but are not limited to, germinating seeds, emerging seedlings, plants that emerge from vegetative propagules, immature vegetation and established vegetation. [000101] As used herein, agriculturally acceptable salts and esters refer to salts and esters which have herbicidal activity, or which are or can be converted to vegetables, water or soil in said herbicides. Exemplary agriculturally acceptable esters are those that are or can be hydrolyzed, oxidized, metabolized or otherwise converted, for example, in plants, water, or soil, to the corresponding carboxylic acid which, depending on the pH, may be in the form dissociated or not dissociated. [000102] Exemplary salts include those derived from alkali or alkaline earth metals and those derived from ammonia and amines. Exemplary cations include sodium, potassium, magnesium and amine cations of the Formula: R1R2R3R4N + where R1, R2, R3 and R4 each independently represent hydrogen or C1-C12 alkyl, C3-C12 alkenyl or C1-C12 alkenyl each one of which is optionally substituted by one or more groups of hydroxy, C1-C4 alkoxy, C1-C4 alkylthio or phenyl, provided that R1, R2, R3 and R4 are sterically compatible. In addition, any two of R1, R2, R3 and R4 together can represent an aliphatic bifunctional component containing from one to twelve carbon atoms and up to two oxygen or sulfur atoms. Salts can be prepared by treatment with a metal hydroxide, such as sodium hydroxide, with an amine, such as ammonia, trimethylamine, diethanolamine, 2 methylthiopropylamine, bisalylamine, 2-butoxyethylamine, morpholine, cyclodecylamine, or benzylamine or with benzylamine or a tetraalkylammonium hydroxide, such as tetramethylammonium hydroxide or choline hydroxide. [000103] Exemplary esters include those derived from C1-C12 alkyl, C3-C12 alkenyl, C3-C12 alkynyl or C7-C10 aryl substituted alkyl alcohols, such as methyl alcohol, isopropyl alcohol, 1-butanol, 2-ethyl- hexanol, butoxyethanol, methoxypropanol, allyl alcohol, propargyl alcohol, cyclohexanol or substituted or unsubstituted benzyl alcohols. Benzyl alcohols can be substituted by 1 to 3 substituents independently selected from halogen, C1-C4 alkyl or C1-C4 alkoxy. Esters can be prepared by coupling fatty acids with alcohol, using any number of appropriate activating agents such as those used for peptide couplings such as dicyclohexylcarbodiimide (DCC) or carbonyl diimidazole (CDI); by reacting the acids with alkylating agents such as alkyl halides or alkyl sulfonates in the presence of a base such as triethylamine or lithium carbonate; by reacting the corresponding acid chloride of an acid with an appropriate alcohol; by reacting the corresponding acid with an appropriate alcohol in the presence of an acid catalyst or by transesterification. COMPOSITIONS AND METHODS [000104] Herbicidal compositions comprising a herbicidally effective amount of (a) a compound of Formula (I) are provided herein or an agriculturally acceptable salt or ester thereof, and (b) an ACCase inhibitor. In certain embodiments, the ACCase inhibitor is cletodim, clodinafop-propargyl, cyhalofop-P-butyl, diclofop-methyl, phenoxaprop-P-ethyl, fluazifop-P-butyl, haloxifop-P-methyl, metamifop, pinoxaden, pro- foxidim , quizalofop-P-ethyl, setoxidim or tralcoxidim, or a derivative thereof, for example, salt, carboxylic acid, carboxylate salt, or its ester. [000105] Methods for controlling undesirable vegetation including contact with the vegetation or its location, that is, are adjacent to the vegetation, with or application to soil or water to prevent the emergence or growth of vegetation of a herbicidally quantity, are also provided here of the compound of Formula (I) and (b) an ACCase inhibitor. In certain embodiments, the methods employ the compositions described herein. [000106] Furthermore, in some embodiments, the combination of compound (I) or its agriculturally acceptable salt or ester and ACCase inhibitors or an agriculturally acceptable salt or ester thereof has synergism, for example, the active herbicidal ingredients are more effective in combination than when applied individually. Synergism was defined as "an interaction of two or more factors such that the effect when combined is greater than the effect predicted based on the response of each factor applied separately". Senseman, S., ed. Herbicide Handbook. 9th ed. Lawrence: Weed Science Society of America, 2007. In certain embodiments, the compositions show synergy as determined by Colby's equation. Colby, S.R. 1967. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 15: 20-22. [000107] In certain embodiments of the compositions and methods described herein, the compound of Formula (I), that is, carboxylic acid, is employed. In certain embodiments, a carboxylate salt of the compound of Formula (I) is employed. In certain embodiments, an aralkyl or alkyl ester is employed. In certain embodiments, a benzyl, substituted benzyl, or C1-C4 alkyl, for example, n-butyl ester, is employed. In certain embodiments, the benzyl ester is used. [000108] In some embodiments, the compound of Formula (I) or its salt or ester and ACCase inhibitor are formulated into a composition, mixed in the tank, applied simultaneously, or applied sequentially. [000109] The herbicidal activity is shown by the compounds when they are applied directly to the plant or to the plant's location at any stage of growth. The observed effect depends on the plant species to be controlled, the growth stage of the plant, the application parameters of dilution and spray droplet size, the particle size of the solid components, the environmental conditions at the time of use, the compound specific used, the specific adjuvants and vehicles used, the type of soil, and more, as well as the amount of chemical product applied. These and other factors can be adjusted to promote non-selective or selective herbicidal action. In some embodiments, the compositions described here are applied as a post-emergence application, a pre-emergence application or an application in flooded rice water or bodies of water (for example, tanks, lakes and streams), in undesirable vegetation relatively immature to achieve maximum weed control. [000110] In some embodiments, the compositions and methods provided herein are used to control weeds in crops, including, but not limited to, rice, cereals, wheat, barley, oats, rye, sorghum, corn, cane -sugar, sunflower, rapeseed, canola, beet, soy, cotton, pineapple, pastures, lawns, pastures, abandoned land, peat, trees and vines, aquatic, crops, vegetables, industrial vegetation management (IVM) and easements ( ROW) sown by no-tillage, water-planting or transplanted. [000111] In certain embodiments, the compositions and methods provided here are used to control weeds in rice. In certain modalities, rice is rice that is sown directly, sown in water, or transplanted. [000112] The compositions and methods described herein can be used to control undesirable vegetation in cultures tolerant to glyphosate, tolerant to 5-enolpyruvylchiquimate-3-phosphate (EPSP), tolerant to glufosinate, tolerant to glutamine synthetase inhibitor, tolerant dicamba, tolerant to phenoxy auxin, tolerant to pyridyloxy auxin, tolerant to auxin, tolerant to auxin transport inhibitor, tolerant to aryloxyphenoxypropionate, tolerant to cyclohexanedione, tolerant to phenylpyrazoline, tolerant to the CoA carboxylase inhibitor (ACCase ), imidazolinone tolerant, sulfonylurea tolerant, pyrimidinylthiobenzoate tolerant, triazolopyrimidine tolerant, sulphonylaminocarbonyltriazolinone tolerant, triazolopyrimidine tolerant, sulfonylaminocarbonyltriazolinone tolerant to hydrolyzate inhibitor (AHAS), tolerant to 4-hydroxy-phenyl-pyruvate dio inhibitor - xigenase (HPPD), tolerant to the phytoene desaturase inhibitor, tolerant to the carotenoid biosynthesis inhibitor, tolerant to the protoporphyrinogen oxidase inhibitor (PPO), tolerant to the cellulose biosynthesis inhibitor, tolerant to the mitosis inhibitor, tolerant to the microtubule inhibitor , tolerant to very long chain fatty acid inhibitor, tolerant to fatty acid and lipid biosynthesis inhibitor, tolerant to photosystem I inhibitor, tolerant to photosystem II inhibitor, tolerant to triazine and tolerant to bromoxynil (such as, but not limited to these, soy, cotton, canola / rapeseed, rice, cereals, corn, sorghum, sunflower, sugar beet, sugar cane, grass, etc.), for example, together with glyphosate, EPSP synthase, glufosinate, glutamine synthase inhibitors, dicamba, phenoxy auxins, pyridyloxy auxins, synthetic auxins, auxin transport inhibitors, aryloxyphenoxypropionates, cyclohexanediones, phenylpyrazolines, ACCase inhibitors, imidazolinones, sulfonylureas, pyrimidinylthiobenzoates, dimethoxy-pyrimidines, triazolopyrimidine sulfonamides, sulfonylaminocarbonyltriazolinones, ALS or AHAS inhibitors, HPPD inhibitors, inhibitors of phyto-inhibitors, phyto-inhibitors, inhibitors , cellulose biosynthesis inhibitors, mitosis inhibitors, microtubule inhibitors, very long chain fatty acid inhibitors, fatty acid and lipid biosynthesis inhibitors, photosystem I inhibitors, photosystem II inhibitors, PPO inhibitors, triazines and bromoxynil. The compositions and methods can be used to control undesirable vegetation in crops that have multiple or concentrated traits that confer tolerance to various chemicals and / or inhibitors of multiple modes of action. In some embodiments, the compound of Formula (I) or its salt or ester and the complementary herbicide or its salt or ester are used in combination with herbicides that are selective for the crop being treated and that complement the spectrum of controlled weeds by these compounds at the application rate employed. In some embodiments, the compositions described herein and other complementary herbicides are applied at the same time, as a combination formulation, tank mix or sequentially. [000113] The compositions and methods that can be used to control undesirable vegetation in crops that have tolerance to agronomic stress (including, but not limited to, drought, cold, heat, salt, water, nutrients, fertility, pH) , pest tolerance (including, but not limited to, insects, fungi and pathogens) and traits of crop improvement (including, but not limited to, production; protein, carbohydrate or oil content; protein, carbohydrate or plant stature and plant architecture). [000114] The compositions and methods provided here are used to control undesirable vegetation. Undesirable vegetation includes, but is not limited to, undesirable vegetation that occurs in rice, cereals, wheat, barley, oats, rye, sorghum, corn, sugar cane, sunflower, rapeseed, canola, sugar beet, soy , cotton, pineapple, natural pasture and pastures, lawns, abandoned land, grass, trees and grape orchards, aquatic, crops, vegetables, industrial vegetation management (IVM) and easements (ROW). [000115] In some embodiments, the methods provided here are used to control undesirable vegetation in rice. In certain modalities, the undesirable vegetation is Brachiaria platyphylla (Gro-seb.) Nash or Urochloa platyphylla (Nash) R.D. Webster (leafy brachiaria, BRAPP), Digitaria sanguinalis (L.) Scop. (large vegetable grass, DIGSA), Echinochloa species (ECHSS), Echinochloa crus-galli (L.) P. Beauv. (backyard grass, ECHCG), Echinochloa crus-pavonis (Kunth) Schult, (gulf spur, ECHCV), Echinochloa colonum (L.) LINK (bush rice, ECHCO), Echinochloa oryzoides (Ard.) Fritsch (grass of the early water, ECHOR), Echinochloa oryzicola (Vasinger) Vasinger (late water grass, ECHPH), Echinochloa phyllopogon (Stapf) Koso-Pol. (rice grass, ECHPH), Echinochloa polystachya (Kunth) Hitchc. (lowland grass, ECHPO), Ischaemum rugosum Salisb. (saramollagrass, ISCRU), Leptochloa chinensis (L.) Nees (Chinese sprangletop, LEFCH), Leptochloa fascicularis (Lam.) Gray (bearded sprangletop, LEFFA), Leptochloa panicoides (Presl.) Hitchc. (Amazon sprangletop, LEFPA), Oryza species (red rice and weed-like, ORYSS), Panicum dichotomiflorum (L.) Michx. (fali panicum, PANDI), Paspalum dilatatum Poir. (dallisgrass, PASDI), Rottboellia cochinchinensis (Lour.) W.D. Clayton (capim-camalote, ROOEX), Cyperus species (CYPSS), Cyperus difformis L. (smallflower flatsedge, CYPDI), Cyperus dubius Rottb. (MAPDU), Cyperus esculentus L. (junquinho, CYPES), Cyperus would L. (rice flatsedge, CYPIR), Cyperus rotundus L. (tiririca, CYPRO), Cyperus serotinus ROTTB./CBClarke (CYPSE), Eleocharis species (ELOSS ), Fimbris-tylis miliacea (L.) Vahl (globe fringerush, FIMMI), Schoenoplectus species (SCPSS), Schoenoplectus Juncoides Roxb. (Japanese reed, SCPJU), Bolboschoenus maritimus (L.) Palla or Schoenoplectus marimimus L. Lye (sea clubrush, SCPMA), Schoenoplectus mucronatus L. (rice reed, SCPMU), Aeschynomene species, (jointvetch, AESSS), Alternanthera philoxeroides (Mart.) Griseb. (alligator weed, ALRPH), Alisma plantago-aquatica L. (common plantago, ALSPA), Amaranthus species, (carurus and amaranth, AMASS), Ammannia coccine Rottb. (red stem, AMMCO), Commelina benghalensis L. (Benghal dayflower, COMBE), Eclipta alba (L.) Hassk. (American false daisy, ECLAL), Heteranthera limosa (SW.) Willd./Vahl (duck salad, HETLI), Heteranthera reniformis R. & P. (Round-leaf iodine banana, HETRE), Ipomoea species (morning glory, IPOSS ), Ipomoea hederacea (L.) Jacq. (ivy morning glory, IPOHE), Lindernia dubia (L.) Pennell (minor false chickweed, LIDDU), Ludwigia species (LUDSS), Ludwigia linifolia Poir. (southeast willow primrose, LUDLI), Ludwigia octovalvis (Jacq.) Raven (long fruity willow primrose, LUDOC), Monochoria korsakowii Regel & Maack (monorail, MOOKA), Vaginal monochorea (Burm. F.) C. Presl ex Kuhth, (monorail, MOOVA), Murdannia nudiflora (L.) Brenan (doveweed, MUDNU), Polygonum pensylvanicum L., (Pennsylvania showy weed, POLPY), Polygonum persicaria L. (ladysthumb, POLPE), Polygonum hydropipe - Michx roides. (POLHP, gentle showy weed), Rotala indica (Willd.) Koehne (Indian toothcup, ROTIN), Sagittaria species, (arrowhead, SAGSS), Sesbania exaltata (Raf.) Cory / Rydb. Ex Hill (sesbania hemp, SEBEX), or Sphenoclea zeylanica Gaertn. (goose weed, SPDZE). [000116] In some modalities, the methods provided here are used to control undesirable vegetation in cereals. In certain modalities, the undesirable vegetation is Alopecurus myosuroides Huds. (black grass, ALOMY), Apera spica-venti (L.) Beauv. (grass of the wind, APESV), Avena fatua L. (wild oats, AVEFA), Bro- mus tectorum L. (woolly bromine, BROTE), Lolium multiflorum Lam. (ryegrass, LOLMU), Phalaris minor Retz. (seedless seed, PHAMI), Poa annua L. (annual grasses, POANN), Setaria pumila (Poir.) Roemer & J.A. Schultes (yellow foxtail grass, SETLU), Setaria viridis (L.) Beauv. (green foxtail grass, SETVI), Amaranthus retroflexus L. (caruru, AMARE), Brassica species (BRSSS), Chenopodium album L. (common lambsquarters, CHEAL), Cirsium arvense (L.) Scop, (Canada thistle, CIRAR), Galium aparine L. (catchweed bedstraw, GALAP), Kochia scoparia (L.) Schrad. (kochia, KCHSC), Lamium purpureum L. (purple dead nettle, LAMPU), Matricaria recutita L. (wild chamomile, MATCH), Matricaria matricarioides (Less.) Porter (pineapple weed, MATMT), Papaver rhoeas L. (common poppy, PAPRH), Polygonum convolvulus L. (wild buckwheat, POLCO), Salsola tragus L. (Russian thistle, SASKR), S / - napis species (SINSS), Sinapis arvensis L. (wild mustard, SINAR) Stellaria media (L.) Vill. (common chickweed, STE-ME), Veronica Persian Poir. (Persian veronica, VERPE), Viola arvensis Murr. (field violet, VIOAR), or Viola tricolor L. (wild violet, VIOTR). [000117] In some modalities, the methods provided here are used to control undesirable vegetation in natural pastures and pastures, abandoned lands, IVM and ROW. In certain embodiments, the undesirable vegetation is Ambrosia artemisiifolia L. (common ambrosia, AMBEL), Cassia obtusifolia (sickle cell, CASOB), Centaurea maculosa auct. non Lam. (spotted centaurea, CENMA), Cirsium arvense (L.) Scop, (Canada thistle, CIRAR), Convolvulus arvensis L. (field vine, CONAR), Daucus carota L. (wild carrot, DAUCA), Euphorbia esula L. (leafy euphorbia, EPHES), Lactuca seriola L./Torn. (prickly lettuce, LACSE), Plantago lanceolata L. (banana deer horn, PLALA), Rumex obtusifolius L. (leafy sorrel, RUMOB), Sida spinosa L. (prickly aids, SIDSP), Sinapis arvenisis L. (wild mustard, SINAR), Sonchus arvensis L. (perennial thistle, SONAR), Solidago species (golden reed, SOOSS), Taraxacum officinale GH Weber ex Wiggers (dandelion, TAROF), Trifolium repens L. (white clover, TRFRE), or Urtica dioica L. (common nettle, URTDI). [000118] In some embodiments, the methods provided here are used to control undesirable vegetation found in row crops, trees and vine crops and perennial crops. In certain modalities, the undesirable vegetation is Alopecurus myosuroides Huds. (black grass, ALOMY), Avena fatua L. (wild oats, AVEFA), Brachiaria decumbens Stapf. or Urochloa decumbens (Stapf) R.D. Webster (grass from Suriname, BRADO), Brachiaria brizantha (Hochst. ex A. Rich.) Stapf. or Urochloa brizantha (Hochst. ex A. Rich.) R.D. (grass beard, BRABR), Brachiaria platyphylla (Groseb.) Nash or Urochloa platyphylla (Nash) R.D. Webster (leafy brachiaria, BRAPP), Brachiaria plantaginea (Link) Hitchc. or Urochloa plantaginea (Link) R.D. Webster (alexandergrass, BRAPL), Cenchrus echinatus L. (southern tick, CENEC), Digitaria horizontalis Willd. (Japanese digarian, DIGHO), Digitaria insularis (L.) Mez ex Ekman (bitter grass, TRCIN), Digitaria sanguinalis (L.) Scop. (large digita, DIGSA), Echinochloa crus-galli (L.) P. Beauv. (grass, ECHCG), Echinochloa colonum (L.) Link (jungle rice, ECHCO), Eleusine indica (L.) Gaertn. (potentilla, ELEIN), Lolium multiflorum Lam. (ryegrass, LOLMU), Panicum dichotomiflorum Michx. (fali panicum, PANDI), Panicum miliaceum L. (wild millet, PANMI), Setaria faberi Herrm. (giant fox tail, SETFA), Setaria viridis (L.) Beauv. (green fox tail, SETVI), Sorghum halepense (L.) Pers. (Johnsongrass, SORHA), Sorghum bicolor (L.) Moench ssp. Arundinaceum (shattercane, SORVU), Cyperus esculentus L. (junquinho, CYPES), Cyperus rodundus L. (tiririca, CYPRO), Abutilon theophrasti Medik. (velvetleaf, ABUTH), Amaranthus species (cururus and amarantus, AMASS), Ambrosia artemisiifolia L. (common ambrosia, AMBEL), Ambrosia psilostachya DC. (western ambrosia, AMBPS), Ambrosia trifida L. (giant ambrosia, AMBTR), Anoda cristata (L.) Schlecht. (spurred anoda, ANVCR), Asclepias syriaca L. (common milkweed, ASCSY), Bidens pilosa L. (black sting, BIDPI), Borreria species (BOISS), Borreria alata (Aubl.) DC. or Spermacoce alata Aubl. (hardwood bud, BOILF), Spermacose latifolia (broadleaf bud, BOILF), Chenopodium album L. (common lambsquarters, CHEAL), Cirsium arvense (L.) Scop, (Canada thistle, CIRAR), Commelina benghalensis L (tropical tradescence, COMBE), Datura stramonium L. (datura, DATST), Daucus cauleta L. (wild carrot, DAUCA), Euphorbia heterophylla L. (dairy, EPHHL), Euphorbia hirta L. or Chamaesyce hirta (L .) Millsp. (garden shrub, EPHHI), Euphorbia dentata Michx. (toothed euphorbia, EPHDE), Erigeron bonariensis L. or Conyza bonariensis (L.) Cronq. (hairy pulicaria, ERIBO), Erigeron canadensis L. or Conyza canadensis (L.) Cronq. (Canadian pulicaria, ERICA), Conyza sumatrensis (Retz.) E. H. Walker (high pulicaria, ERIFL), Helianthus annuus L. (common sunflower, HELAN), Jacquemontia tamnifolia (L.) Griseb. (small-flowered morning glory, IAQTA), Ipomoea hederacea (L.) Jacq. (ivy ipomea, IPOHE), Ipomoea lacunosa L. (white morning glory, IPOLA), Lactuca serrola L./Torn. (prickly lettuce, LACSE), Portulaca oleracea L. (common purslane, POROL), Richardia species (pusley, RCHSS), Sida species (sida, SIDSS), Sida spinosa L. (prickly sida, SIDSP), Sinapis arvensis L. ( wild mustard, SINAR), Solanum ptychanthum Dunal (eastern nightshade, SOLPT), Tridax procumbens L. (coat buttons, TRQPR), Tridax procumbens L. (coat buttons, TRQPR), or Xanthium strumarium L. (thistle common, XANST). used to control undesirable vegetation on the grass. In certain embodiments, the undesirable vegetation is Bellis perennis L. (English daisy, BELPE), Cyperus esculentus L. (junquinha, CYPES), Cyperus species (CYPSS), Digitaria sanguinalis (L.) Scop. (large digita, DIGSA), Diodia virginiana L. (American bud herb, DIQVI), Euphorbia species (spurge, EPHSS), Glechoma hederacea L. (soil ivy, GLEHE), Hydrocotyle umbellata L. (dollar, HYDUM), Kyllinga species (kyllinga, KYLSS), Lamium amplexicaule L. (henbit, LAMAM), Murdania nudiflora (L.) Brenan (doveweed, MUDNU), Oxalis species (wood chestnut, OXASS), Plantago major L. (hardwood banana, PLAMA), Plantago lanceolata L. (banana deer horn / narrow leaf, PLALA), Phyllanthus urinaria L. (chamberbitter, PYLTE), Rumex obtusifolis L. (leafy sorrel, RUMOB), Stachys floridana Shuttlew. (Florida beton, STAFL), Stellaria media (L.) Vill. (common chickweed, STEME), Taraxacum officinale G.H. Weber ex Wiggers (dandelion, TAROF), Trifolium repens L. (white clover, TRFRE), or Viola species (wild violet, VIOSS). [000119] In some embodiments, the methods provided here are used to control undesirable vegetation [000120] In some embodiments, the compositions and methods provided here are used to control undesirable vegetation consisting of pasture, leafy and peppery weeds. In certain embodiments, the compositions and methods provided here are used to control undesirable vegetation, including Avena, Brachiaria, Cyperus, Digitaria, Echinochloa, Fimbristylis, Ipomoea, Ischaumum, Leptochloa, Lolium, Schoenoplectus and Sesbania. [000121] In some embodiments, the combination of compound (I) or its agriculturally acceptable ester or salt and ACCase inhibitors or its agriculturally acceptable salt or ester, is used to control Avena fatua L. (wild oats, AVEFA), Brachiaria platyphylla (Griseb.) Nash (leafy branch, BRAPP), Cyperus difformis L. (small flower umbrella joint, CYPDI), Cyperus esculentus L. (junk, CYPES), Cyperus vai L. (flat rice field, CYPIR), Cyperus rotundus L. (tiririca, CYPRO), Digitaria sanguinalis (L.) Scop, (digitaria grande, DIGSA), Echinochloa crus-galli (L.) Beauv. (grass, ECHCG), Echinochloa colona (L.) Link (jungle rice, ECHCO), Fimbristylis miliacea (L.) Vahl (globe fringerush, FIMMI), Ipomoea hederacea Jacq. (ivy hypomeia, IPOHE), Ischaemum rugosum Salisb. (saramolla- grass, ISCRU), Leptochloa chinensis (L.) Nees (Chinese sprangletop, LEFCH), Lolium multiflorum Lam. (ryegrass, LOLMU), Schoenoplectus Juncoides (Roxb.) Palia (Japanese reed, SCPJU), Schoenoplectus mar- itimusus (L.) Lye (sea clubrush, SCPMA), Schoenoplectus mucronatus (rice papyrus, SCPMU) and Sesbania exaltata (Sesbania hemp, SEBEX). [000122] The compounds of Formula I or its agriculturally acceptable salt or ester can be used to control herbicide resistant or tolerant weeds. The methods that employ the combination of a Formula I compound or its agriculturally acceptable salt or ester and the compositions described herein can also be employed to control herbicide resistant or tolerant weeds. Exemplary resistant or tolerant weeds include, but are not limited to, biotypes resistant or tolerant to acetolactate synthase (ALS) inhibitors or acetohydroxy acid (AHAS) synthase (eg, imidazolinones, sulfonylureas, pyrimidinylthiobenzoates , triazolopyrimidines, sulfonylaminocarbonyl-triazolinones), photosystem II inhibitors (for example, phenylcarbates, pyridazinones, triazines, triazinones, uracils, amides, ureas, benzothiadiazinones, nitriles, phenylpyridazine (ACC) inhibitors (acylase) , aryloxyphenoxypropionates, cyclohexanediones, phenylpyrazolinea), synthetic auxins (eg benzoic acids, phenoxycarboxylic acids, pyridine carboxylic acids, quinoline carboxylic acids), auxin transport inhibitors (eg phthalates, semicarbazones), photosystem inhibitors (for example, bipyridyliums), 5-enolpyruvylchiquimate-3-phosphate (EPSP), synthase inhibitors (po eg glyphosate), glutamine synthetase inhibitors (eg glufosinate, bialafos), microtubule assembly inhibitors (eg benzamides, benzoic acids, dinitroanilines, phosphoramidates, pyridines), mitosis inhibitors (eg carbamates ), very long-chain fatty acid (VLCFA) inhibitors (eg acetamides, chloroacetamides, oxyacetamides, tetrazolines), inhibitors of fatty acid and lipid synthesis (eg phosphorodithioates, thiocarbamates, benzofurans, chlorocarbonic acids), protoporphyrinogen oxidase (PPO) inhibitors (for example, diphenyl ethers, N-phenylphthalimides, oxadiazoles, oxazolidinediones, phenylpyrazoles, pyrimidindiones, thiadiazoles, triazolinones), carotenoid biosynthesis inhibitors, for example, starches, anilidex, furanones, phenoxybutan-amides, pyridiazinones, pyridines), 4-hydroxy-phenyl-pyruvate-dioxigenase (HPPD) inhibitors (for example, calistemones, isoxazoles , pyrazoles, tricetones), cellulose biosynthesis inhibitors (for example, nitriles, benzamides, quincyl, triazolocarboxamides), mitosis inhibitors, cellulose bisynthesis inhibitors, herbicides with multiple modes of action such as quinclorac, and herbicides unclassified such as arylamino-propionic, difenzoquat, endotal, and organoarsenic acids. Exemplary resistant or tolerant weeds include, but are not limited to, biotypes with resistance or tolerance to multiple herbicides, biotypes with resistance or tolerance to multiple chemical classes, biotypes with resistance or tolerance to multiple modes of action, and herbicide biotypes with multiple resistance or tolerance mechanisms (for example, resistance to the target site or metabolic resistance). acceptable compound (I) is employed. In certain embodiments, an agriculturally acceptable ester is employed. In certain embodiments, the ester is a C1-4 alkyl ester. In certain embodiments, the ester is an n-butyl ester. In certain embodiments, the ester is a benzyl ester. In certain embodiments, compound (I), which is a carboxylic acid, is employed. [000123] In some embodiments, an agriculturally acceptable ester or salt of the compound (i) used. [000124] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with clethodim or its salt or ester. With respect to compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to clethodim or its salt or ester is within the range of about 1: 140 to about 9: 1 . In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to clethodim or its salt or ester is within the range of about 1:48 to about 3: 1. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its benzyl or n-butyl ester and clethodim. Regarding the methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to the soil or water to prevent the appearance or growth of vegetation of a composition described here. In some embodiments, the composition is applied at a rate of about 20 grams of active ingredient per hectare (g ia / ha) to about 580 g ia / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 20 grams of active ingredient per hectare (g ia / ha) to about 260 g ai / ha, based on the total amount of active ingredients in the composition. In some modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation with a compound of Formula (I) or its salt or ester and clethodim or its salt, for example for example, sequentially or simultaneously. In some embodiments, clethodim or its salt is applied at a rate of about 17.5 g ai / ha to about 280 g ai / ha, and the compound of Formula (I) or its salt or ester is applied in a rate of about 2 g ea / ha to about 300 g ea / ha. In some embodiments, clethodim or its salt is applied at a rate of about 70 g ai / ha to about 280 g ai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 8 g ea / ha to about 32 g ea / ha. In certain embodiments, the methods use the compound of Formula (I), or its benzyl or n-butyl ester and clethodim for the control of BRAPP, DIGSA, CYPES and SCPJU. [000125] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with clodinafop-propargyl or its salt, carboxylate salt, carboxylic acid or ester. With respect to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to clodinafop-propargyl or its salt, carboxylate salt, carboxylic acid or ester, is within the range of about 1:40 to about 60: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to clodinafop-propargyl or its salt, carboxylate salt, carboxylic acid or ester is within the range of 1:36 to about 10: 1 . In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to clodinafop-propargyl or its salt, carboxylate salt, carboxylic acid or ester is within the range of 1: 6 to about 1: 1 , 5. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its benzyl or n-butyl ester and clodinafop-propargyl. With respect to the methods, in certain modalities, the methods of understanding the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation of a composition described herein. In some embodiments, the composition is applied at a rate of about 7 grams of active ingredient per hectare (g ia / ha) and about 380 g ia / ha, based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 20 grams of active ingredient per hectare (g ia / ha) and about 40 g ia / ha, based on the total amount of active ingredients in the composition. In some modalities, the methods include the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation with a compound of Formula (I) or its salt or ester and clodinafop-propargyl or its salt, carboxylate salt, carboxylic acid or ester, for example, sequentially or simultaneously. In some embodiments, clodinafop-propargyl or its salt, carboxylate salt, carboxylic acid or ester is applied at a rate of about 5 g ai / ha to about 80 g ai / ha, and the compound of Formula (I) , or its salt or ester is applied at a rate of about 2 g ea / ha to about 300 g ea / ha. In some embodiments, clodinafop-propargyl or its salt, carboxylate salt, carboxylic acid or ester is applied at a rate of about 15 g ai / ha to about 30 g ai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 5 g ea / ha to about 10 g ea / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and clodinafop-propargyl is used to control LOLMU, KCHSC, PHAMI, APESV and ALOMY. [000126] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with cyhalofop-R-butyl or its carboxylic acid, carboxylate salt, or ester. With regard to compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to cyhalofop-R-butyl carboxylic acid, carboxylate salt or its ester is within the range of about 1 : 155 to about 6: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to cyhalofop-R-butyl or its carboxylic acid, carboxylate salt or ester is within the range of 1:32 to about 1: 4 . In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to cyhalofop-R-butyl or its carboxylic acid, carboxylate salt or ester is within the range of about 1:42 to about 10 :1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to cyhalofop-R-butyl or its carboxylic acid, carboxylate salt or ester is within the range of about 1:21 to about 5 :1. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its benzyl ester and cyhalofop-R-butyl. In one embodiment, the composition comprises the compound of Formula (I) and cyhalofop-R-butyl, wherein the weight ratio of the compound of Formula (I) to cyhalofop-R-butyl is about 1: 20.6 to about 1: 2.5. In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) and cyhalofop-R-butyl, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to cyhalofop-R-butyl is about from 1:23 to about 5: 1. Regarding the methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or the application to the soil or water to prevent the appearance or growth of vegetation of a composition described here. In some embodiments, the composition is applied at a rate of about 52 grams of active ingredient per hectare (g ia / ha) to about 610 g ai / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 99 grams of active ingredient per hectare (g ia / ha) to about 320 g ai / ha based on the total amount of active ingredients in the composition. In some modalities, the methods include the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation with a compound of Formula (I) or its salt or ester and cyhalofop-R-butyl or its carboxylic acid, carboxylate salt, or ester, for example, sequentially or simultaneously. In some embodiments, the cialofop-R-butyl or its salt or ester is applied at a rate of about 50 g ai / ha and about 310 g ai / ha and the compound of Formula (I) or its salt or ester is applied at a rate of about 2 g ea / ha to about 300 g ea / ha. In some embodiments, the cialofop-R-butyl or its carboxylic acid, carboxylate salt, or ester is applied at a rate of about 45 g ai / ha to about 600 g ai / ha, and the compound of Formula (I ) or its salt or ester is applied at a rate of about 4 g of acid equivalent per hectare (g ea / ha) to about 85 g ea / ha. In some embodiments, cialofop-R-butyl or its carboxylic acid, carboxylate salt or ester is applied at a rate of about 90 g ai / ha to about 300 g ai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 8 g of acid equivalent per hectare (g ea / ha) to about 42 g ea / ha. In certain embodiments, the methods use the compound of Formula (I), or its benzyl ester and cyhalofop-R-butyl. In one embodiment, the methods use the compound of Formula (I) and cyhalofop-R-butyl, in which the compound of Formula (I) is applied at a rate of about 8.75 g of equivalent acid per hectare (g ea / ha) at about 42.4 g ea / ha, and cyhalofop-R-butyl is applied at a rate of about 90 g ai / ha to about 280 g ai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and cyhalofop-R-butyl, in which the benzyl ester of the compound of Formula (I) is applied at a rate of about 8.75 g of acid equivalent per hectare (g ea / ha) to about 35 g ea / ha, and cyhalofop-R-butyl is applied at a rate of about 90 g ai / ha to about 300 g ai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with cyhalofop-R-butyl or its carboxylic acid, carboxylate salt, or ester are used to control ISCRU, IPOHE, ECHOR , SCPSU, LEFCH, SCPMA, CYPIR, FIMMI, SEBEX, CYPDI, ECHCG, ECHSS or SCPMU. [000127] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with diclofop-methyl or its carboxylic acid, carboxylate salt or ester. Regarding the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to diclofop-methyl or its carboxylic acid, carboxylate salt or ester is within the range of about 1: 560 to about 5: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to diclofop-methyl or its carboxylic acid, carboxylate salt or ester is within the range of 1: 255 to about 1: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to diclofop-methyl or its carboxylic acid, carboxylate salt or ester is within the range of 1: 140 to about 1: 9. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its benzyl or n-butyl ester and diclofop-methyl. With respect to the methods, in certain modalities, the methods of understanding the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation of a composition described herein. In some embodiments, the composition is applied at a rate of about 72 grams of active ingredient per hectare (g ia / ha) to about 1420 g ia / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 73 grams of active ingredient per hectare (g ia / ha) to about 610 g ai / ha based on the total amount of active ingredients in the composition. In some embodiments, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation with a compound of Formula (I) or its salt or ester and diclofop-methyl, or its salt or ester, for example, sequentially or simultaneously. In some embodiments, diclofop-methyl or its salt or ester is applied at a rate of about 70 g ai / ha to about 1120 g ai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 2 g ea / ha to about 300 g ea / ha. In certain embodiments, the methods use the compound of Formula (I) or its benzyl or n-butyl ester and diclofop-methyl is used to control APESV, CYPIR, KCHSC and PHAMI. [000128] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with phenoxaprop-P-ethyl or its carboxylic acid or carboxylate salt or other ester, and phenoxaprop- P-ethyl can be applied alone or in combination with isoxadifen-ethyl or mefenpir-diethyl protectors. In relation to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to phenoxaprop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is within the range of about 1 : 170 to about 30: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to phenoxaprop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is within the range of 1:16 to about 1, 5: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to phenoxaprop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is within the range of 1:16 to about 3: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to phenoxaprop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is within the range of about 1:32 to about 4: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to phenoxaprop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is within the range of about 1:16 to about 2: 1. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its benzyl ester and phenoxaprop-P-ethyl. In one embodiment, the composition comprises the compound of Formula (I) and phenoxaprop-P-ethyl, where the weight ratio of the compound of Formula (I) to phenoxaprop-P-ethyl is from about 1:14 to about 2: 1. In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) and phenoxaprop-P-ethyl, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to phenoxaprop-P-ethyl is about 1:16 to about 1: 1. With respect to the methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation of a composition described herein. In some embodiments, the composition is applied at a rate of about 13 grams of active ingredient per hectare (g ia / ha) to about 440 g ia / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 15 grams of active ingredient per hectare (g ia / ha) to about 90 g ai / ha based on the total amount of active ingredients in the composition. In some modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation with a compound of Formula (I) or its salt or ester and phenoxaprop-P-ethyl or its salt or ester, for example, sequentially or simultaneously. In some embodiments, phenoxaprop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is applied at a rate of about 11 g ai / ha to about 140 g ai / ha, and the compound of Formula (I ) or its salt or ester is applied at a rate of about 2 g ea / ha to about 300 g ea / ha. In some embodiments, phenoxaprop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is applied at a rate of about 5 g ai / ha to about 300 g ai / ha, and the compound of Formula (I ) or its salt or ester is applied at a rate of about 2 g of equivalent acid per hectare (g ea / ha) to about 90 g ea / ha. In some embodiments, phenoxaprop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is applied at a rate of about 11.5 g ai / ha to about 140 g ai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 4.38 g of acid equivalent per hectare (g ea / ha) to about 42.4 g ea / ha. In certain embodiments, the methods use the compound of Formula (I), or its benzyl ester and phenoxaprop-P-ethyl. In one embodiment, the methods use the compound of Formula (I) and phenoxaprop-P-ethyl, in which the compound of Formula (I) is applied at a rate of about 4.38 g of equivalent acid per hectare (g ea / ha) at about 42.4 g ea / ha, and phonoxaprop-P-ethyl is applied at a rate of about 11.5 g ai / ha to about 140 g ai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and phenoxaprop-P-ethyl, in which the benzyl ester of the compound of Formula (I) is applied at a rate of about 4.38 g of acid equivalent per hectare (g ea / ha) to about 35 g ea / ha, and phenoxaprop-P-ethyl is applied at a rate of about 17.5 g ai / ha to about 70 g ai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with phenoxaprop-P-ethyl or its carboxylic acid or carboxylate salt or other ester are used to control CYPIR, ECHOR , FIMMI, SCPJU, CYPES, KCHSC, PHAMI and APESV. [000129] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with fluazifop-P-butyl or its carboxylic acid or carboxylate salt or other ester. With respect to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to fluazifop-P-butyl or its carboxylic acid or carboxylate salt or other ester is within the range of about from 1: 210 to about 3: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to fluazifop-P-butyl or its carboxylic acid or carboxylate salt or other ester is within the range of 1:41 to about 2, 5: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to fluazifop-P-butyl or its carboxylic acid or carboxylate salt or other ester is within the range of 1:41 to about 1: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to fluazifop-P-butyl or its salt or ester is within the range of about 1:80 to about 1: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to fluazifop-P-butyl or its salt or ester is within the range of about 1:36 to about 1: 2.5. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its benzyl ester and fluazifop-P-butyl. In one embodiment, the composition comprises the compound of Formula (I) and fluazifop-P-butyl, wherein the weight ratio of the compound of Formula (I) to fluazifop-P-butyl is about 1:36 to about 1: 2.5. In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) and fluazifop-P-butyl, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to fluazifop-P-butyl is about 1:36 to about 1: 5.1. With respect to the methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation of a composition described herein. In some embodiments, the composition is applied at an application rate of about 47 grams of active ingredient per hectare (g ia / ha) to about 720 g ai / ha, based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 50 grams of active ingredient per hectare (g ia / ha) to about 200 g ai / ha based on the total amount of active ingredients in the composition. In some embodiments, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation with a compound of Formula (I) or its salt or ester and fluazifop-P-butyl or its salt or ester, for example, sequentially or simultaneously. In some embodiments, fluazifop-P-butyl or its carboxylic acid or carboxylate salt or other ester is applied at a rate of about 45 g ea / ha to about 420 g ea / ha, and the compound of Formula (I ) or its salt or ester is applied at a rate of about 2 g ea / ha to about 300 g ea / ha. In some embodiments, fluazifop-P-butyl or its carboxylic acid or carboxylate salt or other ester is applied at a rate of about 20 g ai / ha to about 400 g ai / ha, and the compound of Formula (I ) or its salt or ester is applied at a rate of about 2 g of equivalent acid per hectare (g ea / ha) to about 70 g ea / ha. In some embodiments, fluazifop-P-butyl or its carboxylic acid or carboxylate salt or other ester is applied at a rate of about 45 g ai / ha to about 180 g ai / ha, and the compound of Formula (I ) or its salt or ester is applied at a rate of about 4.38 g of acid equivalent per hectare (g ea / ha) to about 35 g ea / ha. In certain embodiments, the methods use the compound of Formula (I), or its benzyl ester and fluazifop-P-butyl. In one embodiment, the methods use the compound of Formula (I) and fluazifop-P-butyl, in which the compound of Formula (I) is applied at a rate of about 4.38 g of equivalent acid per hectare ( g ea / ha) and about 35 g ea / ha, and fluazifop-P-butyl is applied at a rate of about 45 g ai / ha to about 180 g ai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and fluazifop-P-butyl, in which the benzyl ester of the compound of Formula (I) is applied at a rate of about 4.38 g of acid equivalent per hectare (g ea / ha) to about 8.75 g ea / ha, and fluazifop-P-butyl is applied at a rate of about 45 g ai / ha to about 180 g ai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with fluazifop-P-butyl or its carboxylic acid or carboxylate salt or other ester are used to control IPOHE, ECHOR or CYPRO . [000130] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with haloxifop-R-methyl or its carboxylic acid or carboxylate salt or other ester. In relation to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to haloxifop-R-methyl or its carboxylic acid or carboxylate salt or other ester is within the range of about 1 : 45 to about 10: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to haloxifop-R-methyl or its carboxylic acid or carboxylate salt or other ester is within the range of 1: 6 to about 2, 5: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to haloxifop-R-methyl or its carboxylic acid or carboxylate salt or other ester is within the range of about 1:15 to about 6: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to haloxifop-R-methyl or its carboxylic acid or carboxylate salt or other ester is within the range of about 1: 7 to about 2.6: 1. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its benzyl ester and haloxifop-R-methyl. In one embodiment, the composition comprises the compound of Formula (I) and haloxifop-R-methyl, wherein the weight ratio of the compound of Formula (I) to haloxifop-R-methyl is about 1: 6.2 to about 2.6: 1. In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) and haloxifop-R-methyl, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to haloxifop-R-methyl is about 1: 7 to about 1.3: 1. With respect to the methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation of a composition described herein. In some embodiments, the composition is applied at an application rate of about 32 grams of active ingredient per hectare (g ia / ha) to about 420 g ai / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 10 grams of active ingredient per hectare (g ia / ha) to about 60 g ia / ha, based on the total amount of active ingredients in the application composition . In some embodiments, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation with a compound of Formula (I) or its salt or ester and haloxifop-R-methyl or its carboxylic acid or carboxylate salt or other ester, for example, sequentially or simultaneously. In some embodiments, haloxifop-R-methyl or its carboxylic acid or carboxylate salt or other ester is applied at a rate of about 6.75 g ea / ha to about 120 g ea / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 2 g ea / ha to about 300 g ea / ha. In some embodiments, haloxifop-R-methyl or its carboxylic acid or carboxylate salt or other ester is applied at a rate of about 3 g ai / ha to about 140 g ai / ha, and the compound of Formula (I ) or its salt or ester is applied at a rate of about 2 g of acid equivalent per hectare (g ea / ha) to about 45 g ea / ha. In some embodiments, haloxifop-R-methyl or its carboxylic acid or carboxylate salt or other ester is applied at a rate of about 6.75 g ai / ha to about 70 g ai / ha and the compound of Formula ( I) or its salt or ester is applied at a rate of about 4.38 g of acid equivalent per hectare (g ea / ha) to about 17.5 g ea / ha. In certain embodiments, the methods use the compound of Formula (I), or its benzyl or n-butyl ester and haloxifop-R-methyl. In one embodiment, the methods use the compound of Formula (I) and haloxifop-R-methyl, in which the compound of Formula (I) is applied at a rate of about 4.38 g of equivalent acid per hectare (g ea / ha) at about 35 g ea / ha, and haloxifop-R-methyl is applied at a rate of about 6.75 g ai / ha to about 70 g ai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and haloxifop-R-methyl, in which the benzyl ester of the compound of Formula (I) is applied at a rate of about 4.38 g of acid equivalent per hectare (g ea / ha) to about 17.5 g ea / ha, and haloxifop-R-methyl is applied at a rate of about 6.75 g ai / ha to about 27 g ai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with haloxifop-R-methyl or its carboxylic acid or carboxylate salt or other ester are used to control ECHCO, IPOHE, SCPJU , BRAPP or CYPRO. [000131] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with metamifop or its salt or ester. With respect to compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to metamifop or its salt or ester is within the range of about 1: 150 to about 6: 1 . In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to metamifop or its salt or ester is within the range of 1:34 to about 10: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to metamifop or its salt or ester is within the range of 1:34 to about 1: 2. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to metamifop or its salt or ester is within the range of about 1:60 to about 1: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to metamifop or its salt or ester is within the range of about 1:30 to about 1: 2.1. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its benzyl ester and metamifop. In one embodiment, the composition comprises the compound of Formula (I) and metamifop, wherein the weight ratio of the compound of Formula (I) to metamifop is from about 1:30 to about 1: 2.1. In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) and metamifop, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to metamifop is from about 1:30 to about 1: 15. Regarding the methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to the soil or water to prevent the appearance or growth of vegetation of a composition described here. In some embodiments, the composition is applied at an application rate of about 52 grams of active ingredient per hectare (g ia / ha) to about 600 g ai / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 40 grams of active ingredient per hectare (g ia / ha) to about 170 g ia / ha based on the total amount of active ingredients in the composition. In some embodiments, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation with a compound of Formula (I) or its salt or ester and metamifop or its salt or ester, for example, sequentially or simultaneously. In some embodiments, metamifop or its salt or ester is applied at a rate of about 50 g ai / ha to about 300 g ai / ha, and the compound of Formula (I) or its salt or ester is applied in a rate of about 2 g ea / ha to about 300 g ea / ha. In some embodiments, metamifop or its salt or ester is applied at a rate of about 30 g ai / ha to about 300 g ai / ha and the compound of Formula (I) or its salt or ester is applied in a rate of about 2 g of acid equivalent per hectare (g ea / ha) to about 70 g ea / ha. In some embodiments, metamifop or its salt or ester is applied at a rate of about 75 g ai / ha to about 150 g ai / ha and the compound of Formula (I) or its salt or ester is applied at a rate from about 4.38 g of acid equivalent per hectare (g ea / ha) to about 35 g ea / ha. In certain embodiments, the methods use the compound of Formula (I), or its benzyl ester and metamifop. In one embodiment, the methods use the compound of Formula (I) and metamifop, in which the compound of Formula (I) is applied at a rate of about 4.38 g of acid equivalent per hectare (g ea / ha) at about 35 g ea / ha, and metamifop is applied at a rate of about 75 g ai / ha to about 150 g ai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and metamifop, in which the benzyl ester of the compound of Formula (I) is applied at a rate of around 4.38 g of equivalent acid per hectare ( g ea / ha), and metamifop is applied at a rate of about 75 g ia / ha to about 150 g ia / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with metamifop or its salt or ester are used to control IPOHE, ECHCG, ECHOR, IPOHE, FIMMI, SCPMA or SCPJU. [000132] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with pinoxaden or its salt or ester. With respect to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester of pinoxaden or its salt or ester is within the range of about 1:30 to about 150: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pinoxaden or its salt or ester is within the range of 1:27 to about 25: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to pinoxaden or its salt or ester is within the range of 1:12 to about 2: 1. In certain embodiments, the compositions comprise the compound of Formula (I) or its benzyl or n-butyl ester and pinoxaden. With respect to the methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation of a composition described herein. In some embodiments, the composition is applied at an application rate of about 4 grams of active ingredient per hectare (g ia / ha) to about 360 g ai / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 8 grams of active ingredient per hectare (g ia / ha) to about 110 g ai / ha based on the total amount of active ingredients in the composition. In some embodiments, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation with a compound of Formula (I) or its salt or ester and pinoxaden or its salt , for example, sequentially or simultaneously. In some embodiments, pinoxaden or its salt or ester is applied at a rate of about 2 g ai / ha to about 60 g ai / ha and the compound of Formula (I) or its salt or ester is applied in a rate of about 2 g ea / ha to about 300 g ea / ha. In some embodiments, pinoxaden or its salt or ester is applied at a rate of about 15 g ai / ha to about 60 g ai / ha and the compound of Formula (I) or its salt or ester is applied at a rate from about 5 g ea / ha to about 32 g ea / ha. In certain embodiments, the methods use the compound of Formula (I) or its benzyl or n-butyl ester and pinoxaden for the control of ECHCO, IPOHE, KCHSC, PHAMI and SCPJU. [000133] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with profoxidim or its salt or ester. With regard to compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to profoxidim or its salt or ester is within the range of about 1:70 to about 29: 1 . In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to profoxidim or its salt or ester is within the range of 1: 8 to about 2: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to profoxidim or its salt or ester is within the range of about 1:10 to about 3: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to profoxidim or its salt or ester is within the range of about 1:23 to about 3: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to profoxidim or its salt or ester is within the range of about 1: 5 to about 1.4: 1. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its benzyl ester and profoxidim. In one embodiment, the composition comprises the compound of Formula (I) and profoxidim, wherein the weight ratio of the compound of Formula (I) to profoxidim is around 1: 3. In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) and profoxidim, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to profoxidim is from about 1: 5 to about 1, 4: 1. Regarding the methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to the soil or water to prevent the appearance or growth of vegetation of a composition described here. In some embodiments, the composition is applied at an application rate of around 15 grams of active ingredient per hectare (g ia / ha) to about 500 g ai / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 16 grams of active ingredient per hectare (g ia / ha) to about 50 g ai / ha based on the total amount of active ingredients in the composition. In some embodiments, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation with a compound of Formula (I) or its salt or ester and profoxidim or its salt or ester, for example, sequentially or simultaneously. In some embodiments, profoxidim or its salt or ester is applied at a rate of about 12 g ai / ha to about 200 g ai / ha and the compound of Formula (I) or its salt or ester is applied in a rate of about 2 g ea / ha to about 300 g ea / ha. In some embodiments, profoxidim or its salt or ester is applied at a rate of about 4 g ai / ha to about 140 g ai / ha and the compound of Formula (I) or its salt or ester is applied in a rate of about 2 g of acid equivalent per hectare (g ea / ha) to about 45 g ea / ha. In some embodiments, profoxidim or its salt or ester is applied at a rate of about 12.5 g ai / ha to about 25 g ai / ha and the compound of Formula (I) or its salt or ester is applied in a rate of about 4.38 g acid equivalent per hectare (g ea / ha) to about 17.5 g ea / ha. In certain embodiments, the methods use the compound of Formula (I), or its benzyl or n-butyl ester and profoxidim. In one embodiment, the methods use the compound of Formula (I) and profoxidim, in which the compound of Formula (I) is applied at a rate of about 4.38 g of equivalent acid per hectare (g ea / ha), and profoxidim is applied at a rate of around 12.5 g ai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and profoxidim, in which the benzyl ester of the compound of Formula (I) is applied at a rate of about 4.38 g of equivalent acid per hectare ( g ea / ha) at about 17.5 g ea / ha, and profoxidim is applied at a rate of about 12.5 g ai / ha to about 25 g ia / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with profoxidim or its salt or ester are used to control ECHCO, ECHCO, SCPJU or LEFCH. [000134] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with quizalofop-P-ethyl or its carboxylic acid or carboxylate salt or other ester. Regarding the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to quizalofop-P-ethyl or its carboxylic acid or carboxylate salt or another ester is within the range of about 1 : 100 to about 12: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to quizalofop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is within the range of 1: 8 to about 19 :1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to quizalofop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is within the range of 1: 6 to about 1: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to quizolofop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is within the range of about 1:12 to about 10: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to quizalofop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is within the range of about 1: 6 to about 5: 1. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its benzyl ester and quizolofop-P-ethyl. In one embodiment, the composition comprises the compound of Formula (I) and quizalofop-P-ethyl, wherein the weight ratio of the compound of Formula (I) to quizalofop-P-ethyl is about 1: 6 to about 5: 1. In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) and quizalofop-P-ethyl, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to quizalofop-P-ethyl is about 1: 6 to about 5: 1. With respect to the methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation of a composition described herein. In some embodiments, the composition is applied at an application rate of about 6 grams of active ingredient per hectare (g ia / ha) to about 400 g ai / ha, based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 8 grams of active ingredient per hectare (g ia / ha) to about 50 g ai / ha based on the total amount of active ingredients in the composition. In some modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation with a compound of Formula (I) or its salt or ester and quizalofop-P-ethyl or its carboxylic acid or carboxylate salt or other ester, for example, sequentially or simultaneously. In some embodiments, quiza-lopop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is applied at a rate of about 4 g ai / ha to about 100 g ea / ha and the compound of Formula ( I) or its salt or ester is applied at a rate of about 2 g ea / ha to about 300 g ea / ha. In some embodiments, quizalofop-P- or its carboxylic acid or carboxylate salt or other ester is applied at a rate of about 2 g ai / ha to about 60 g ai / ha and the compound of Formula (I) or its salt or ester is applied at a rate of about 2 g of acid equivalent per hectare (g ea / ha) to about 70 g ea / ha. In some embodiments, quizalofop-P-ethyl or its carboxylic acid or carboxylate salt or other ester is applied at a rate of about 3.56 g ai / ha to about 30 g ai / ha and the compound of Formula ( I) or its salt or ester is applied at a rate of about 3.75 g of acid equivalent per hectare (g ea / ha) to about 35 g ea / ha. In certain embodiments, the methods use the compound of Formula (I) or its benzyl ester and quizalofop-P-ethyl. In one embodiment, the methods use the compound of Formula (I) and quizalofop-P-ethyl, in which the compound of Formula (I) is applied at a rate of about 3.75 g of equivalent acid per hectare (g ea / ha) at about 35 g ea / ha, and quizalofop-P-ethyl is applied at a rate of about 3.56 g ai / ha to about 30 g ai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and quizalofop-P-ethyl, in which the benzyl ester of the compound of Formula (I) is applied at a rate of about 3.75 g of acid equivalent per hectare (g ea / ha) to about 17.5 g ea / ha, and quizalofop-P-ethyl is applied at a rate of about 3.56 g ai / ha to about 30 g ai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with quiza-lopop-P-ethyl or its carboxylic acid or carboxylate salt or other ester are used to control IPOHE, ECHOR , CYPRO, ECHCG, AVEFA, LOLMU. [000135] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with setoxidim or its salt or ester. With regard to compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to setoxidim or its salt or ester is within the range of about 1:70 to about 29: 1 . In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to setoxidim or its salt or ester is within the range of 1: 8 to about 2: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to setoxidim or its salt or ester is within the range of about 1:61 to about 1: 2. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to setoxidim or its salt or ester is within the range of about 1: 120 to about 1: 3. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to setoxidim or its salt or ester is within the range of about 1:54 to about 1: 7.7. In certain embodiments, the compositions provided herein comprise the compound of Formula (I) or its benzyl ester and setoxidim. In one embodiment, the composition comprises the compound of Formula (I) and setoxidim, wherein the weight ratio of the compound of Formula (I) to setoxidim is from about 1:54 to about 1: 7,7. In one embodiment, the composition comprises the benzyl ester of the compound of Formula (I) and setoxidim, wherein the weight ratio of the benzyl ester of the compound of Formula (I) to setoxidim is from about 1:27 to about 1: 15.4. Regarding the methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to the soil or water to prevent the appearance or growth of vegetation of a composition described here. In some embodiments, the composition is applied at an application rate of about 55 grams of active ingredient per hectare (g ia / ha) to about 825 g ai / ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 55 grams of active ingredient per hectare (g ia / ha) to about 300 g ai / ha based on the total amount of active ingredients in the composition. In some embodiments, the methods comprise contacting undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation with a compound of Formula (I) or its salt or ester and setoxidim or its salt or ester, for example, sequentially or simultaneously. In some embodiments, setoxidim or its salt or ester is applied at a rate of about 50 g ai / ha to about 525 g ai / ha and the compound of Formula (I) or its salt or ester is applied in a rate of about 2 g ea / ha to about 300 g ea / ha. In some embodiments, setoxidim or its salt or ester is applied at a rate of about 30 g ai / ha to about 600 g ai / ha and the Formula (I) compound or its salt or ester is applied at a rate of about 2 g of acid equivalent per hectare (g ea / ha) to about 45 g ea / ha. In some embodiments, setoxidim or its salt or ester is applied at a rate of about 67.5 g ai / ha to about 270 g ai / ha, and the compound of Formula (I) or its salt or ester is applied at a rate of about 4.38 g of acid equivalent per hectare (g ea / ha) to about 17.5 g ea / ha. In certain embodiments, the methods use the compound of Formula (I), or its benzyl ester and setoxidim. In one embodiment, the methods use the compound of Formula (I) and setoxidim, in which the compound of Formula (I) is applied at a rate of about 4.38 g of acid equivalent per hectare (g ea / ha) at about 17.5 g ea / ha and setoxidim is applied at a rate of about 67.5 g ai / ha to about 270 g ai / ha. In one embodiment, the methods use the benzyl ester of the compound of Formula (I) and setoxidim, in which the benzyl ester of the compound of Formula (I) is applied at a rate of about 4.38 g of equivalent acid per hectare ( g ea / ha) at about 8.75 g ea / ha, and setoxidim is applied at a rate around 135 g ai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with setoxidim or its salt or ester are used to control CYPES, CYPDI, CYPIR, SCPJU, LEFCH, FIMMI or ECHCG. [000136] In certain embodiments of the compositions and methods described herein, the compound of Formula (I) or its salt or ester is used in combination with tralkoxydim or its salt or ester. In relation to the compositions, in some embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to tralcoxidim or its salt or ester is within the range of about 1:38 to about 60: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to tralkoxydim or its salt or ester is within the range of 1:23 to about 10: 1. In certain embodiments, the weight ratio of the compound of Formula (I) or its salt or ester to tralcoxidim or its salt or ester is within the range of 1:40 to about 1: 2. In certain embodiments, the compositions comprise the compound of Formula (I) or its benzyl or n-butyl ester and alkoxydim. With respect to the methods, in certain modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation of a composition described herein. In some embodiments, the composition is applied at an application rate of about 7 grams of active ingredient per hectare (g ia / ha) to about 375 g ai / ha, based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of about 8 grams of active ingredient per hectare (g ia / ha) to about 100 g ai / ha based on the total amount of active ingredients in the application composition. In some modalities, the methods comprise the contact of undesirable vegetation or its location or application to soil or water to prevent the appearance or growth of vegetation with a compound of Formula (I) or its salt or ester and tralcoxidim or a salt thereof , for example, sequentially or simultaneously. In some embodiments, tralcoxidim or its salt or ester is applied at a rate of about 5 g ai / ha to about 75 g ai / ha and the compound of Formula (I) or its salt or ester is applied in a rate of about 2 g ea / ha to about 300 g ea / ha. In certain embodiments, the methods use the compound of Formula (I) or its benzyl or n-butyl ester and tralkoxydim is used to control AVEFA, CYPIR, KCHSC and LOLMU. [000137] The components of the mixtures described here can be applied separately or as part of a multi-component herbicide system. [000138] The mixtures described here can be applied in conjunction with one or more other herbicides to control a wider variety of undesirable vegetation. When used in conjunction with other herbicides, the composition can be formulated with the other herbicide or herbicides, mixed in tank with the other herbicide or herbicides, or applied sequentially with the other herbicide or herbicides. Some of the herbicides that can be used in conjunction with the compositions and methods described herein include, but are not limited to: 4-CPA; 4-CPB; 4-CPP; 2,4-D; 2,4-D choline salt, 2,4-D, 2,4-DB esters and amines; 3,4-DA; 3,4-DB; 2,4-DEB; 2,4-DEP; 3,4-DP; 2,3,6-TBA; 2,4,5-T; 2,4,5-TB; acetochlor, acifluorfen, aclonifen, acrolein, alachlor, alidochlor, aloxidime, allyl alcohol, alorac, ametridione, amethrine, amibuzin, amicarbazone, amidosulfurone, aminocyclopyrachlor, aminopiralid, amiprofos-methyl, amitron, amitron, amitron, sulphate , atrazine, azafenidin, azinsulfurone, aziprotrin, barbana, BCPC, beflubutamid, benazoline, bencarbazone, benfluralin, benfuresate, bensulfuron-methyl, bensulid, bentiocarb, bentazon-sodium, benzadox, benzofend, benzofen, benzofen, benzen , biafa, bicyclopyrone, bifenox, bilanafos, bispiribac-sodium, borax, bromacil, bromobonyl, bromobutide, bromophenoxin, bromoxynil, brompirazon, butachlor, butafenacil, butamiphos, butenachlor, butidonyl, butidonyl, butidonyl, butidonyl, butidonyl, butidonyl, butidonyl, butidonyl, butidonyl, butidonyl, butyronate , cacodylic acid, cafenstrol, calcium chlorate, calcium cyanamide, cambendichlor, carbasulam, carbetamide, carboxazole, chlorprocarb, carfentrazone-ethyl, CDEA, CE PC, chlorotoxifen, chloramben, chloranocril, chlorazifop, chlorazine, chlorobromuron, chlororburon, chloreturon, chlorphenac, clorfenprop, chlorflurazole, chlorflurenol, chloridazon, chlorimuron, chlorornitrophen, chloropon, chlorotoluron, chloroxuron, chloroxurur, chloroxuron cinidon-ethyl, cinmetilina, cinosulfuron, cisanilide, cliodinato, clofop, clomazone, clomeprop, cloprop, cloproxidim, clopyralid, cloransulam-methyl, CMA, copper sulphate, CPMF, CPPC, credazine, cresol, cumiluron, cyanatrin, cyanatrin, cyanatrin cyclopyrimorate, cyclosulfamuron, cycloxydim, cycluron, cyperquat, cyprazine, cyprazole, cipromid, daimuron, dalapon, dazomet, delaclor, demedipham, desmetrine, dialate, dicamba, diclobenil, dichloro-dichloro, dichloro, dichloro, dichloro, dichloro, dichloro, dichloro, dichloro, dichloro, dichloro, quat, dietathyl, difenopenten, difenoxuron, difenzoquat, diflufenican, diflufenzopyr, dimefuron, dimepiperate, dimetachlor, dimetamethrin, dimethamide, dimethenamide-P, dimexane, dimidazon, di nitramine, dinofenate, dinoprop, dinosam, dinoseb, dinoterb, diphenamid, dipropetrin, diquat, disul, dithiopir, diuron, DMPA, DNOC, DSMA, EBEP, eglinazine, endotal, epronaz, EPTC, erbon, esprocarb, etalfluralina, etbenzamide, etametsulfuron, etidimuron, etiolate, etobenzamid, etobenzamid, ethofumesate, ethoxyfen, ethoxysulfuron, ethinophen, etnipromid, etobenzanide, EXD, fenasulam, feneno, fenoxassulfone, fentaclor, fentacloride, fentacloride, fentacloride, fentacen -M, flazassul-furon, florassulam, fluazolate, flucarbazone, flucethosulfuron, fluclora- lin, flufenacet, flufenican, flufenpir-ethyl, flumetsulame, flumezin, flumi- chlorac-pentyl, flumioxazin, flumipropine, flumipropine, fluometuron, fluometuron , flúornitrofen, fluotiuron, flupoxam, flupropacil, flupropanato, flupirsulfuron, fluridone, fluorochloridone, fluroxypyr, fluroxy-pir-meptila, flurtamone, flutiaceto, fomesafen, foramsulfuron, phosamine, fumiclorac, glumoxin, fur glufosinate-ammonium, glufosinate-P-ammonium, salts and esters of glyphosate, halauxifen, halauxifen-methyl, halosafe n, halosulfuron-methyl, haloxidine, hexachloroacetone, hexaflurate, hexazinone, imazametabenzo, imazamyazur, imazamyazyz, , imazetapyr, indanofan, indaziflam, iodobonyl, iodomethane, iodosulfuron, iodosulfuron-ethyl-sodium, iofensulfuron, ioxinol, ipazine, ipfencarbazone, iprimidam, isocarbamid, isocyl, isomer, isopropyl, isopropyl, isopropyl, isopropyl, isopropyl, isopropyl, isopropyl, isopropyl, isopropyl, isopropyl, , isoxaben, isoxaclortol, isoxaflutol, isoxapirifop, carbutilate, ketoespiradox, lactofen, lenacil, linuron, MAA, MAMA, esters and amines MCPA, MCPA-thioethyl, MCPB, mecoprop, mecoprop-P, medinoterb, mefena, mefena, mesoprazine, mesosulfuron, mesotrione, metam, metamitron, metazachlor, metazosulfuron, metflurazon, metabenztiazuron, metalpropalin, metazol, metiobencarb, methiozoline, metiuron, methomon, methoprotrin, methyl bromide, isothiocyanate, isothiocyanate methyl, methyldinon, metobenzuron, metobromuron, metolachlor, metosulam, methoxy-ron, metribuzin, metsulfuron, metsulfuron-methyl, molinate, monalide, monisouron, monochloroacetic acid, monolinuron, monuron, morphan-napramide, MSMA , neburon, nicosulfuron, nipyraclofen, nitralin, nitrofen, nitrofluorfen, norflurazon, noruron, OCH, orbencarb, ortho-dichlorobenzene, orthosulfamuron, orizalin, oxadiargil, oxadiazon, oxapirazon, oxaduron, oxoxururon, oxoxururon, oxoxururon, oxicluron, oxoxururon, oxoxururon, , pebulate, pelargonic acid, pendimethalin, penoxsulam, pentachlorophenol, pentanochlor, pentoxa-zone, perfluidone, petoxamide, fenisofam, fenemedifame, fenemedifa-me-ethyl, fenobenzuron, phenylmercury acetate, picloram, picolinafen, arzoline, potassium, picolinafen, polina potassium, potassium cyanide, pretilachlor, primisulfuron-methyl, prociazine, prodiamine, profluazole, pro-fluralin, proglinazine, proexadione-calcium, promethrin, pronamide, propaclor, propanil, propaquizafop, propazine, profam, propisochlor, propoxycarbazone, propyrisulfuron, propizamide, prosulfalin, prosulfo-carb, prosulfuron, proxan, prinachlor, pidanon, piraclonil, piraflufen-ethyl, pirassulfotol, pirazograzole, pirazogolazole ethyl, pyrazoxyphen, pyribenzoxy, pyributicarb, pyrichloride, pyridafol, pyridate, pyriftalide, pyriminobac, pyrimisulfan, pyritazac-sodium, pyroxassulfone, pyroxsulam, quinclorac, quinmerac, quinoclamine, quinonamide, rhodetanil, rhodanil, rinethanol, rhodanil, rinulin, rhodanil, rinulin, rhodanil, rhodinol, rinet, rilan, ril. sebutilazine, secbumeton, siduron, simazine, simeton, symmetrine, SMA, sodium arsenite, sodium azide, sodium chloride, sulcotrione, sulfalate, sulfentrazone, sulfometuron, sulfosate, sulfosulfuron, sulfuric acid, sulglicapin, swep, SYN-523 , TCA, tebutamon, tebutiuron, tefuriltrione, tembotrione, tepraloxidim, terbacil, terbuclorb, terbuclor, terbumeton, terbutilazine, terbutrin, tetrafluron, tenilflor, thiazafluron, thiazopyr, thidiazine , tidiazuron, tiencarbazone-methyl, tifensulfuron, tifensulfurn-methyl, thiobencarb, tiocarbazil, thioclorin, topramezone, triafamone, tri-alate, triasulfuron, triaziflam, tribenuron, tribenuron and triclin, triluron-triclin, is triclin, triclin and triclin tri- clopyr, tridifane, trietazine, trifloxysulfuron, trifluralin, triflussulfuron, trifop, trifopsime, trihydroxytriazine, trimeturon, tripropindan, tritosacsulfuron, vernolate, xylachlor and salts, esters, and these esters. [000139] The compositions and methods described herein, can also be used in conjunction with glyphosate, 5-enolpyruvylchiquimate-3-phosphate (EPSP) synthase inhibitors, glufosinate, glutamine synthetase inhibitors, dicamba, phenoxy auxins, pyridyloxy auxins , synthetic auxins, auxin transport inhibitors, aryloxyphenoxypropionates, cyclohexanediones, phenylpyrazolines, acetyl CoA carboxylase (ACCase) inhibitors, imidazolinones, sulfonylureas, pyrimidinylthiobenzoates, triazolopyrimidine sulfonamide and sulfonamide inhibitors acetohydroxy acid (AHAS), 4-hydroxyphenyl-pyruvate dioxigenase (HPPD) inhibitors, phytene desaturase inhibitors, carotenoid biosynthesis inhibitors, protoporphyrinogen oxidase (PPO) inhibitors, cellulose biosynthesis inhibitors, mitosis inhibitors microtubules, very long-chain fatty acid inhibitors, biosynthesis inhibitors of fatty acid and lipid, photosystem I inhibitors, photosystem II inhibitors, triazines, and bromoxynil in cultures tolerant to glyphosate, tolerant to EPSP synthase inhibitor, tolerant to glufosinate, tolerant to glutamine synthetase inhibitor, tolerant to dicamba, tolerant to dicamba phenoxy auxin, tolerant to pyridyloxy auxin, tolerant to auxin, tolerant to auxin transport inhibitor, tolerant to aryloxyphenoxypropionate, tolerant to cyclohexanedione, tolerant to phenylpyrazoline, tolerant to ACCase, tolerant to imidazolinone, tolerant to sulfonylurea, tolerant to pyronylurea - diniltiobenzoate, tolerant to triazolopyrimidine, tolerant to sulfonylminocarbonyltriazolinone, tolerant to (ALS) or AHAS, tolerant to HPPD, tolerant to the phytene desaturase inhibitor, tolerant to the carotenoid biosynthesis inhibitor, tolerant to PPO inhibitors, tolerant to the inhibition of PPO inhibitors cellulose, tolerant to mitosis inhibitor, tolerant to m icrotubules, tolerant to very long chain fatty acid inhibitor, tolerant to fatty acid and lipid biosynthesis inhibitor, tolerant to photosystem I inhibitor, tolerant to photosystem II inhibitor, tolerant to triazine and tolerant to bromoxynil, and cultures that have multiple or concentrated features that provide tolerance to various chemicals and / or various modes of action through individual and / or multiple resistance mechanisms. In some embodiments, the compound of Formula (I) or its salt or ester and the complementary herbicide or its salt or ester are used in combination with herbicides that are selective for the crop being treated and that complement the spectrum of weeds controlled by them compounds at the application rate employed. In some embodiments, the compositions described herein and other complementary herbicides are applied at the same time, either as a combination formulation or as a tank mixture. [000140] In some embodiments, the compositions described herein are used in combination with one or more herbicide protectors, such as AD-67 (MON 4660), benoxacor, bentiocarb, brassinolide, cloquintocet (mexila), ciometrinil, daimuron, diclormid, dicyclonon, dimepiperate, disulfoton, fenclorazol-ethyl, fenclorin, flurazol, fluxofenin, furilazole, harpine proteins, isoxadifen-ethyl, jiecaowan, jiecaoxi, mefenpir-diethyl, mefenate, amine; of N-phenylsulfonylbenzoic acid, to enhance its selectivity. In some modalities, protectors are used in the fixation of rice, cereal, or corn. In some embodiments, the protector is cloquintocet or an ester or salt thereof. In certain embodiments, cloquintocet is used to antagonize the harmful effects of the compositions on rice and cereals. In some modalities, the protector is cloquintocet (mexila). [000141] In some embodiments, the compositions described herein are used in combination with one or more plant growth regulators, such as 2,3,5-triiodiodobenzoic acid, IAA, IBA, naphthalene acetamide, α-naphthalene acetic acids, benzyladenine , 4-hydroxyphenethyl alcohol, kinetin, zeatin, endotal, etefon, pentachlorophenol, tidiazuron, tribufos, aviglycine, maleic hydrazide, gibberellins, gibberellic acid, abscisic acid, ancimidol, phosamine, glyphosine, isopyimimid, maleic acid, jasmine , mepiquat, 2,3,5-triiodiobenzoic acid, morphactins, dichlorflurenol, flurprimidol, mefluidide, paclobutrazol, tetciclacis, uniconazole, brassinolide, brassinolideo-ethyl, cycloheximide, ethylene, metassulfocarb, proexadine and trexexyamine, trexapexine and trexadine. [000142] In some modalities, plant growth regulators are used in one or more crops or settlements, such as rice, cereal crops, corn, leafy crops, rapeseed / canola, grass, pineapple, sugar cane , sunflower, pastures, lawns, pastures, abandoned land, grape trees and orchards, crops, vegetables and non-agricultural (ornamental) settlements. In some embodiments, the plant growth regulator is mixed with the compound of Formula (I), or mixed with the compound of Formula (I) and ACCase inhibitors to cause a preferentially beneficial effect on plants. [000143] In certain embodiments, the compositions comprise or the methods use (a) the compound of Formula I or its agriculturally acceptable salt or ester; (b) an ACCase inhibitor; and (c) a third herbicide. In some embodiments, the compositions comprise or methods use a compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and penoxsulam. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 7 to about 45 weight percent of the total composition; cyhalofop-butyl is about 48 to about 89 weight percent of the total composition, and penoxsulam is about 4 to about 7 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 9 to about 28 weight percent of the total composition; cyhalofop-butyl is about 62 to about 88 weight percent of the total composition, and penoxsulam is about 2 to about 10 weight percent of the total composition. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha (grams of acid equivalent / ha); cialofop-butyl or its salt or ester is applied at a rate of about 25 to about 400 g ai / ha (grams of active ingredient / ha), and penoxsulam is applied from about 1 to about 50 g ai / ha (grams of active ingredient / ha). In another embodiment, the compound of Formula I, or its agriculturally acceptable salt or ester, is applied at a rate of about 1 to about 32 g ea / ha; cialofop-butyl or its salt or ester is applied at a rate of about 25 to about 280 g ai / ha, and penoxsulam is applied from about 2 to about 35 g ai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with cyhalofop-butyl and penoxsulam, or its salt or ester, are used to control ECHCG, CYPRO and FIMMI. [000144] In some embodiments, the compositions comprise or methods use a compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and bentazone-sodium. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 2 to about 13 weight percent of the total composition; cyhalofop-butyl is about 14 to about 20 weight percent of the total composition, and bentazon-sodium is about 73 to about 78 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 1 to about 9 weight percent of the total composition; cyhalofop-butyl is about 15 to about 18 weight percent of the total composition, and bentazone-sodium is about 78 to about 84 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cialofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and benta-zone-sodium is applied from about 1 to about 1500 g ai / ha. In another embodiment, the compound of Formula I, or its agriculturally acceptable salt or ester, is applied at a rate of about 1 to about 32 g ea / ha; cialofop-butyl or its salt or ester is applied at a rate of about 25 to about 280 g ai / ha, and bentazone-sodium is applied from about 210 to about 1200 g ai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with cyhalofop-butyl and sodium bentazone, or its salt or ester, are used to control ECHCG and FIMMI. [000145] In some embodiments, the compositions comprise or methods use a compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and triclopyr. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 2 to about 20 weight percent of the total composition; cyhalofop-butyl is about 20 to about 22 weight percent of the total composition, and bentazone-sodium is about 58 to about 78 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 1 to about 11 weight percent of the total composition; cyhalofop-butyl is about 15 to about 25 weight percent of the total composition, and triclopyr is about 64 to about 84 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cyhalofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and triclopyr is applied from about 100 to about 840 g ea / ha. In another embodiment, the compound of Formula I, or its agriculturally acceptable salt or ester, is applied at a rate of about 1 to about 32 g ea / ha; cialofop-butyl its salt or ester is applied at a rate of about 25 to about 280 g ai / ha, and triclopyr is applied from about 210 to about 560 g ea / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with cyhalofop-butyl and triclopyr, or its salt or ester, are used to control ECHCG and SCPJU. [000146] In some embodiments, the compositions comprise or the methods use a compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and bispiribac-sodium. In some embodiments, the Formula I compound or its agriculturally acceptable salt or ester is about 4 to about 44 weight percent of the total composition; cyhalofop-butyl is about 47 to about 53 weight percent of the total composition, and bispiribac-sodium is about 9 to about 43 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 6 to about 28 weight percent of the total composition; cyhalofop-butyl is about 60 to about 63 weight percent of the total composition, and bispiribac-sodium is about 11 to about 30 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cyhalofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and bispiribac-sodium is applied from about 20 to about 90 g ai / ha. In another embodiment, the compound of Formula I, or its agriculturally acceptable salt or ester, is applied at a rate of about 1 to about 32 g ea / ha; cyhalofop-butyl or its salt or ester is applied at a rate of about 25 to about 280 g ai / ha, and bispiribac-sodium is applied from about 25 to about 75 g ai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with cyhalofop-butyl and bispiribac-sodium, or its salts or esters, are used to control ECHCG and SCPJU. or methods use the compound of Formula I, cyhalofop-butyl, and imazamox. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 5 to about 44 weight percent of the total composition; cyhalofop-butyl is about 46 to about 77 weight percent of the total composition, and imazamox is about 10 to about 18 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 8 to about 28 weight percent of the total composition; cyhalofop-butyl is about 58 to about 80 weight percent of the total composition, and imazamox is about 12 to about 14 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ai / ha; cialofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and imazamox is applied from about 6 to about 70 g ai / ha. [000147] In some embodiments, the compositions comprise or the methods use the compound of Formula I, [000148] In some embodiments, the compositions comprise or the methods use a compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and benzobicyclon. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 3 to about 33 weight percent of the total composition; cyhalofop-butyl is about 32 to about 35 weight percent of the total composition, and benzobicyclon is about 33 to about 65 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 3 to about 19 weight percent of the total composition; cyhalofop-butyl is about 32 to about 42 weight percent of the total composition, and benzobicyclon is about 39 to about 65 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ai / ha; cialofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and benzobicyclon is applied from about 50 to 300 g ai / ha. In another embodiment, the compound of Formula I, or its agriculturally acceptable salt or ester, is applied at a rate of about 1 to about 32 g ea / ha; cyhalofop-butyl or its salt or ester is applied at a rate of about 25 to about 280 g ai / ha, and benzobicyclon is applied from about 50 to about 300 g ai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with cyhalofop-butyl and bispyribac-sodium, or its salt or ester, are used to control ECHCG, ECHOR and FIMMI. [000149] In some embodiments, the compositions comprise or methods use a compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl and quinclorac. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 2 to about 25 weight percent of the total composition; cyhalofop-butyl is about 25 to about 27 weight percent of the total composition, and quinclorac is about 48 to about 72 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 3 to about 14 weight percent of the total composition; cyhalofop-butyl is about 25 to about 26 weight percent of the total composition, and quinclorac is about 54 to about 71 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cialofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and quinclorac is applied from about 70 to about 560 g ai / ha. [000150] In some embodiments, the compositions comprise or the methods use a compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and glyphosate. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 1 to about 11 weight percent of the total composition; cyhalofop-butyl is about 11 to about 13 weight percent of the total composition, and glyphosate is about 78 to about 86 weight percent of the total composition. In certain embodiments the compound of Formula I or its agriculturally acceptable salt or ester is about 1.5 to about 5.5 weight percent of the total composition; cyhalofop-butyl is about 15 to about 11.5 weight percent of the total composition, and glyphosate is about 83 to about 83.5 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cyhalofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and glyphosate is applied from about 160 to about 2240 g ea / ha. [000151] In some embodiments, the compositions comprise or methods use a compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and glufosinate. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 4 to about 14 weight percent of the total composition; cyhalofop-butyl is about 15 to about 45 weight percent of the total composition, and glufosinate is about 51 to about 71 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 4 to about 7 weight percent of the total composition; cyhalofop-butyl is about 16 to about 38 weight percent of the total composition, and glufosinate is about 58 to about 77 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cyhalofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and glufosinate is applied from about 28 to about 1560 g ai / ha. [000152] In some embodiments, the compositions comprise or methods use a compound of Formula I or its agriculturally acceptable salt or ester, phenoxaprop, and penoxsulam. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 7 to about 61 weight percent of the total composition; phenoxaprop is about 89 to about 29 weight percent of the total composition, and penoxsulam is about 4 to about 10 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 9 to about 44 weight percent of the total composition; fenoxaprop is about 41 to about 88 weight percent of the total composition, and penoxsulam is about 3 to about 15 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; fenoxaprop is applied at a rate of about 25 to about 140 g ea / ha, and penoxsulam is applied from about 1 to about 50 g ai / ha. [000153] In some embodiments, the compositions comprise or the methods use a compound of Formula I or its agriculturally acceptable salt or ester, metamifop, and penoxsulam. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 4 to about 46 weight percent of the total composition; metamifop is about 46 to about 94 weight percent of the total composition, and penoxsulam is about 2 to about 8 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 7 to about 30 weight percent of the total composition; metamifop is about 60 to about 90 weight percent of the total composition, and penoxsulam is about 3 to about 10 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; metamifop is applied at a rate of about 10 to about 300 g ea / ha, and penoxsulam is applied from about 1 to about 50 g ai / ha. In another embodiment, the compound of Formula I, or its agriculturally acceptable salt or ester, is applied at a rate of about 1 to about 32 g ea / ha; metamifop, or its salt or ester, is applied at a rate of about 25 to about 100 g ai / ha, and penoxsulam is applied from about 5 to about 35 g ai / ha. In certain embodiments, methods and compositions using the compound of Formula (I) or its salt or ester in combination with metamifop and penoxsulam, or its salt or ester, are used to control ECHCG. [000154] In some embodiments, the compositions comprise or the methods use a compound of Formula I or its agriculturally acceptable salt or ester, profoxidim and penoxsulam. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 13 to about 55 weight percent of the total composition; profoxidim is about 36 to about 80 weight percent of the total composition, and penoxsulam idiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 19 to about 39 weight percent of the total composition; profoxidim is about 50 to about 74 weight percent of the total composition, and penoxsulam is about 3 to about 10 weight percent of the total composition. In some embodiments, the compound of Formula I, or a salt or ester thereof, is applied at a rate of about 2 to about 300 g ea / ha; profoxidim is applied at a rate of about 12 to about 200 g ai / ha, and penoxsulam is applied from about 1 to about 50 g ai / ha. or the methods use a compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and benfuresate. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 2 to about 32 weight percent of the total composition; cyhalofop-butyl is about 34 to about 35 weight percent of the total composition, and benfuresate is about 33 to about 64 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 3 to about 19 weight percent of the total composition; cyhalofop-butyl is about 32 to about 42 weight percent of the total composition, and benfuresate is about 39 to about 64 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cyhalofop-butyl, is applied at a rate of about 25 to about 400 g ai / ha, and benfuresate is applied from about 50 to 300 g ai / ha. [000155] In some embodiments, the compositions comprise or methods use a compound of Formula I or its agriculturally acceptable salt or ester, [000156] In some embodiments, the compositions comprise or methods use a compound of Formula I or its agriculturally acceptable salt or ester of cyhalofop-butyl and fentrazamide. In some embodiments, the Formula I compound or its agriculturally acceptable salt or ester is about 5 to about 33 weight percent of the total composition; cyhalofop-butyl is about 35 to about 58 weight percent of the total composition, and fentrazamide is about 32 to about 37 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 6 to about 19 weight percent of the total composition; cyhalofop-butyl is about 39 to about 63 weight percent of the total composition, and fentrazamide is about 31 to about 40 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cyhalofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and fentrazamide is applied from about 16 to about 300 g ai / ha. [000157] In some embodiments, the compositions comprise or the methods use a compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and indanofan. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 4 to about 33 weight percent of the total composition; cyhalofop-butyl is about 35 to about 48 weight percent of the total composition, and indanofan is about 32 to about 48 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 5 to about 19 weight percent of the total composition; cyhalofop-butyl is about 42 to about 48 weight percent of the total composition, and indanofan is about 39 to about 48 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cyhalofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and indanofan is applied from about 25 to about 300 g ai / ha. [000158] In some embodiments, the compositions comprise or methods use a compound of Formula I or its agriculturally acceptable salt or ester, [000159] In some embodiments, the compositions comprise or the methods use a compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and mefenacet. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 1 to about 14 weight percent of the total composition; cyhalofop-butyl is about 9 to about 14 weight percent of the total composition, and mefenacet is about 72 to about 90 weight percent of the total composition. In certain embodiments, Formula I is about 2 to about 7 weight percent of the total composition; cyhalofop-butyl is about 14 to about 16 weight percent of the total composition, and mefenacet is about 77 to about 85 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cialofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and mefenacet is applied from about 250 to about 1600 g ai / ha. In another embodiment, the compound of Formula I, or its agriculturally acceptable salt or ester, is applied at a rate of about 1 to about 32 g ea / ha; cialofop-butyl or its salt or ester is applied at a rate of about 25 to about 280 g ai / ha, and mefenacet is applied from about 75 to about 560 g ai / ha. [000160] In some embodiments, the compositions comprise or the methods use a compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and oxaziclomafone. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 6 to about 43 weight percent of the total composition; cyhalofop-butyl is about 42 to about 76 weight percent of the total composition, and oxazyclomaphone is about 11 to about 18 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 7 to about 27 weight percent of the total composition; cyhalofop-butyl is about 58 to about 77 weight percent of the total composition, and oxazyclomaphone is about 14 to about 15 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cyhalofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and oxaziclomafone is applied from about 6 to about 80 g ai / ha. In some embodiments, the compositions comprise or methods use a compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, or pretilachlor. [000161] In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 3 to about 22 weight percent of the total composition; cyhalofop-butyl is about 23 to about 38 weight percent of the total composition, and pretilachlor is about 55 to about 58 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 3 to about 13 weight percent of the total composition; cyhalofop-butyl is about 26 to about 32 weight percent of the total composition, and pretilachlor is about 61 to about 65 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cyhalofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and pretilachlor is applied from about 38 to about 750 g ai / ha. [000162] In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and propyrisulfuron. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 5 to about 42 weight percent of the total composition; cyhalofop-butyl is about 44 to about 66 weight percent of the total composition, and propyrisulfuron is about 14 to about 29 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 7 to about 26 weight percent of the total composition; cyhalofop-butyl is about 56 to about 66 weight percent of the total composition, and propyrisulfuron is about 18 to about 27 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cyhalofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and propyrisulfuron is applied from about 11 to about 100 g ai / ha. [000163] In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and pyraclonil. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 1 to about 33 weight percent of the total composition; cyhalofop-butyl is about 12 to about 33 weight percent of the total composition, and pyraclonil is about 33 to about 87 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 2 to about 19 weight percent of the total composition; cyhalofop-butyl is about 20 to about 42 weight percent of the total composition, and pyraclonil is about 39 to about 78 weight percent of the total composition. In some modalities, the compound of Formula I, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cyhalofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and pi-raclonil is applied from about 180 to about 300 g ai / ha. [000164] In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl, and pyriftalid. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 3 to about 42 weight percent of the total composition; cyhalofop-butyl is about 35 to about 45 weight percent of the total composition, and pyriftalid is about 13 to about 62 weight percent of the total composition. In certain embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 5 to about 27 weight percent of the total composition; cyhalofop-butyl is about 47 to about 57 weight percent of the total composition, and pyriftalid is about 16 to about 48 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate from about 2 to about 300 g ea / ha; cialofop-butyl is applied at a rate of about 25 to about 400 g ai / ha, and pyriftalid is applied from about 45 to about 90 g ai / ha. [000165] In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester, cyhalofop-butyl and pyrimisulfan. In some embodiments, the compound of Formula I or its agriculturally acceptable salt or ester is about 7 to about 46 weight percent of the total composition; cyhalofop-butyl is about 48 to about 85 weight percent of the total composition, and pyrimisulfan is about 6 to about 8 weight percent of the total composition. In certain embodiments, Formula I is about 9 to about 29 weight percent of the total composition; cyhalofop-butyl is about 63 to about 84 weight percent of the total composition, and pyrimisulfan is about 7 to about 8 weight percent of the total composition. In some embodiments, the Formula I compound, or its salt or ester, is applied at a rate of about 2 to about 300 g ea / ha; cyhalofop-butyl is applied at a rate of about 25 to about 320 g ai / ha, and pyrimissulfan is applied from about 2.5 to about 40 g ai / ha. [000166] In some embodiments, the compositions described herein are used in combination with one or more herbicide protectors, such as AD-67 (MON 4660), benoxacor, bentiocarb, brassinolide, cloquintocet (mexila), ciometrinil, daimuron, diclormid, dicyclonon, dimepiperate, disulfoton, fenclorazol-ethyl, fenclorim, flurilazol, fluoxofenim, flurilazole, harpine proteins, isoxadifen-ethyl, jiecaowan, jiecaoxi, mefenpir-diethyl, mefenpirido, NA, nefe and N-phenylsulfonylbenzoic acid amides, to enhance their selectivity. In some embodiments, the protector is cloquintocet or an ester or salt thereof. In certain embodiments, cloquintocet is used to antagonize the harmful effects of the compositions on rice and cereals. In some modalities, the protector is cloquintocet (mexila). [000167] In some embodiments, the compositions provided here still comprise at least one agriculturally acceptable adjuvant or vehicle. Suitable adjuvants or vehicles should not be phytotoxic to valuable crops, particularly at the concentrations used in applying the compositions for the selective control of weeds in the presence of crops, and should not react chemically with the herbicidal components or other ingredients in the composition. Such mixtures can be designed for direct application to weeds or their location, or they can be concentrated or formulations that are usually diluted with additional vehicles and adjuvants before application. They can be solids, such as, for example, powders, granules, water-dispersible granules, or wetting powders, or liquids, such as, for example, emulsifiable concentrates, solutions, emulsions or suspensions. They can also be supplied as a premix or tank mix. [000168] Suitable agricultural adjuvants and vehicles include, but are not limited to, culture oil concentrate; nonylphenol ethoxylate; benzylcocoalkyl dimethyl quaternary ammonium salt; mixture of petroleum hydrocarbon, alkyl esters, organic acid, and anionic surfactant; C9-C11 alkyl polyglycoside; phosphated alcohol ethoxylate; natural primary alcohol ethoxylate (C12-C16); EO-PO di-seg-butylphenol block copolymer; polysiloxane-methyl layer; nonylphenol ethoxylate + ammonium urea nitrate; emulsified methylated seed oil; tridecyl alcohol (synthetic) ethoxylate (8EO); tallow amine ethoxylate (15 EO); PEG (400) dioleate-99. [000169] Liquid vehicles that can be used include water and organic solvents. Organic solvents include, but are not limited to, petroleum or hydrocarbon fractions such as mineral oil, aromatic solvents, paraffinic oils, and more, vegetable oils such as soybean oil, rapeseed oil, olive oil, castor, sunflower seed oil, coconut oil, corn oil, cottonseed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil, tung oil and more; the esters of the vegetable oils above; esters of dihydric, trihydric, or lower monoalcohols or polyalcohols (containing 4-6 hydroxy), such as 2-ethyl hexyl stearate, n-butyl oleate, isopropyl myristate, propylene glycol dioleate , di-octyl succinate, di-butyl adipate, di-octyl phthalate and more; esters of mono-, di- and polycarboxylic acids and more. Specific organic solvents include, but are not limited to, estem toluene, xylene, petroleum naphtha, crop oil, acetone, methyl ethyl ketone, cyclohexanone, trichlorethylene, perchlorethylene, ethyl acetate, amyl acetate, butyl acetate, monomethyl propylene glycol ether and monomethyl diethylene ether, methyl alcohol, ethyl alcohol, isopropyl alcohol, amyl alcohol, ethylene glycol, propylene glycol, glycerin, N-methyl-2-pyrrolidinone, N, N-dimethyl alkylamides, dimethyl sulfoxide, fertilizers liquids and more. In certain embodiments, water is the vehicle for diluting concentrates. [000170] Suitable solid vehicles include, but are not limited to, talc, pyrophyllite clay, silica, atapulgite clay, kaolin clay, kieselguhr, chalk, diatomaceous earth, lime, calcium carbonate, bentonite clay, Fuller earth, cotton shells, wheat flour, soy flour, pumice stone, sawdust, nutshell flour, lignin, cellulose, and more. [000171] In some embodiments, the compositions described here still comprise one or more surfactants. In some embodiments, such surfactants are employed in both solid and liquid compositions, and in certain embodiments those designed to be diluted with a vehicle prior to application. Surfactants can be anionic, cationic or non-ionic in character and can be used as emulsifying agents, wetting agents, suspending agents, or for other purposes. Surfactants that can also be used in the present formulations are described, inter alia, in “McCutcheon's Detergents and Emulsifiers Annual,” MC Publishing Corp., Ridgewood, New Jersey, 1998 and in “Encyclopedia of Surfactants,” Vol. I-III, Chemical Pu-blishing Co., New York, 1980-81. Surfactants include, but are not limited to, alkyl sulfate salts, such as diethanolammonium lauryl sulfate; alkylarylsulfonate salts, such as calcium dodeci- Ibenzenesulfonate; alkylphenol-alkylene oxide addition products, such as nonylphenol-Cie ethoxylate; alcohol-alkylene oxide addition products, such as ethoxylated Ciθ-tridecyl alcohol; soaps, such as sodium stearate; alkyl naphthalene sulfonate salts, such as sodium dibutyl naphthalenesulfonate; dialkyl esters of sulfosuccinate salts, such as sodium sulfosuccinate di (2-ethylexyl); sorbitol esters, such as sorbitol oleate; quaternary amines, such as lauryl trimethylammonium chloride; polyethylene glycol esters of fatty acids, such as polyethylene glycol stearate; block copolymers of ethylene oxide and propylene oxide; salts of mono- and dialkyl phosphate esters; vegetable or seed oils such as soybean oil, rapeseed / canola oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cottonseed oil, linseed oil, palm oil , peanut oil, safflower oil, sesame oil, tung oil and more; and esters of the above vegetable oils, and in certain embodiments, methyl esters. [000172] In some embodiments, these materials, such as vegetable or seed oils and their esters, can be used interchangeably as an agricultural adjuvant, as a liquid carrier or as a surfactant. [000173] Other exemplary additives for use in the compositions provided herein include, but are not limited to, compatibilizing agents, defoaming agents, sequestering agents, neutralizing and buffering agents, corrosion inhibitors, tinctures, fragrances, blowing agents, auxiliaries penetration agents, fixing agents, dispersing agents, thickening agents, freezing point depressants, antimicrobial agents, and more. The compositions can also contain other compatible components, for example, other herbicides, plant growth regulators, fungicides, insecticides and more and can be formulated with liquid or solid fertilizers, particulate fertilizer vehicles such as ammonium nitrate, urea and others more. [000174] In some embodiments, the concentration of the active ingredients in the compositions described here is about 0.0005 to 98 weight percent. In some embodiments, the concentration is about 0.0006 to 90 weight percent. In compositions designed to be employed as concentrates, the active ingredients, in certain embodiments, are present in a concentration of about 0.1 to 98 weight percent, and in certain embodiments about 0.5 to 90 weight percent. Such compositions are, in certain embodiments, diluted with an inert carrier, such as water, prior to application. The diluted compositions generally applied to weeds or the weed site contain, in certain embodiments, about 0.0006 to 10.0 weight percent of active ingredient and in certain embodiments contain from about 0.01 to 5.0 percent by weight. [000175] The present compositions can be applied to weeds or in their place using conventional sprinklers, sprayers and soil or aerial granule applicators, through the addition in irrigation water or rice paddy, and by other known conventional means by those skilled in the art. [000176] The modalities described and the following examples are for illustrative purposes and are not intended to limit the scope of king-vindications. Other modifications, uses or combinations in relation to the compositions described herein will be evident to a person of practical skill in the technique without departing from the spirit and scope of the object claimed. Examples [000177] The results of Examples I, II, III, IV VI and VII are the results of experiments in the greenhouse. Example I. Evaluation of Herbicidal Mixtures Applied to Post-emergence Leaves for Weed Control in No-Till Rice [000178] Seeds or small nuts of the desired test plant species were planted in a soil matrix prepared by mixing a clay or sandy clay soil (for example, 28.6 percent mud, 18.8 percent clay, and 52.6 percent sand, with a pH around 5.8 and an organic matter content around 1.8 percent) and limestone sand in a ratio of 80 to 20. The soil matrix was contained in pots of plastic with a volume of 1 liter (1 quarter gallon) and a surface area of 83.6 square centimeters (cm2). When required to ensure good germination and healthy plants, a fungicide treatment and / or other chemical or physical treatment was applied. The plants were grown for 8 to 22 days in a greenhouse with a photoperiod of approximately 14 h which was kept at around 29 ° C during the day and 26 ° C at night. The nutrients (Peters Excel® 15-5-15 5-Ca 2-Mg and iron chelate) were applied to the irrigation solution when necessary and water was added on a regular basis. Supplementary lighting was provided with 1000 Watt metal halide suspended lamps when needed. The plants were used for testing when they reached the first to the fourth authentic leaf stage. [000179] The treatments consisted of 4- amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxy-phenyl) pyridine-2-carboxylic acid or esters (Compound A) , each formulated as a SC (suspension concentrate), and various herbicidal components alone and in combination. Compound A forms were applied on an equivalent acid base. [000180] The forms of compound A (compound of Formula I) tested include: Benzyl Ester of Compound A [000181] Other herbicidal components were applied on an acid equivalent (ae) or active ingredient (ai) basis and included acetyl coA carboxylase (ACCase) inhibiting herbicides (cyclohexanedione and aryloxyphenoxypropionate) chemical classes. -butyl formulated as Clincher® SF (285 gai / L EC), diclofop-methyl formulated as Hoelon® 3EC, phenoxaprop-p-ethyl + isoxadifenethyl formulated as RiceStar® HT (0.58 Ib / gal EC), fenoxaprop- p- ethyl + mefenpir diethyl formulated as Puma® 1EC, metamifop formulated as Metamifop EC, haloxifop-methyl formulated as Gallant Super®, fluazifop-p-butyl formulated as Fusilade® DX, quizalofop-p-ethyl formulated as Assure® II, profoxidim formulated as Aura® 20EC, clethodim applied as Intensity®, setoxidim formulated as Poast®, and tralcoxidim formulated as Achieve®. [000182] The treatment requirements were calculated based on the rates being tested, the concentration of active ingredient or acid equivalent in the formulation, and an application volume of 12 mL at a rate of 187 L / ha. [000183] For treatments comprised of formulated compounds, measured amounts of compounds were placed individually in 25 ml_ glass bottles and diluted in a volume of 1.25% (v / v) of concentrated Agri-Dex® culture oil for obtain 12X raw material solutions. If a test compound does not dissolve easily, the mixture is heated and / or subjected to ultrasound. The application solutions were prepared by adding an appropriate amount of each raw material solution (for example, 1 ml) and diluted to the appropriate final concentrations with the addition of 10 ml of a 1.25% (v / v) culture oil concentrate so that the final spray solutions contain 1.25 +/- 0.05% (v / v) culture oil concentrate. [000184] For treatments comprised of technical compounds, weighted amounts can be placed individually in 25 ml glass vials and dissolved in a volume of 97: 3 v / v acetonine / DMSO to obtain 12X raw material solutions. If a test compound does not dissolve easily, the mixture can be heated and / or subjected to ultrasound. Application solutions can be prepared by adding an appropriate amount of each raw material solution (for example, 1 ml) and diluted to the appropriate final concentrations with the addition of 10 ml of a 1.5% aqueous mixture (v / v) of culture oil concentrate so that the final spray solutions contain 1.25% (v / v) of culture oil concentrate. When technical materials are used, concentrated raw material solutions can be added to the spray solutions so that the final concentrations of acetone and DMSO in the application solutions are 16.2% and 0.5%, respectively. [000185] For treatments comprised of formulated and technical compounds, weighted amounts of technical materials can be placed individually in 25 ml glass vials and dissolved in a 97: 3 v / v acetone / DMSO volume to obtain matter solutions -12X, and measured quantities of the formulated compounds can be placed individually in 25 ml glass bottles and diluted in a volume of 1.5% (v / v) of culture oil or water concentrate to obtain raw material solutions press 12X. If a test compound does not dissolve easily, the mixture can be heated and / or subjected to ultrasound. Application solutions can be prepared by adding an appropriate amount of each raw material solution (eg 1 ml) and diluted to the appropriate final concentrations with the addition of an appropriate amount of an aqueous mixture of 1.5 % (v / v) of culture oil concentrate so that the final spray solutions contain 1.25% (v / v) of culture oil concentrate. As required, additional water and / or 97: 3 v / v acetone / DMSO can be added to the individual application solutions so that the final concentrations of acetone and DMSO of the application solutions being compared are 8.1% and 0, 25%, respectively. [000186] All raw material solutions and application solutions were visually inspected for compatibility of the compound prior to application. The spraying solutions were applied to the plant material with a drop-out spray from Mandei equipped with a nozzle 8002E calibrated to release 187 L / ha over an application area of 0.503 m2 at a spray height of 46 to 50 cm (18 to 20 inches) above the average height of the canopy of the plant. The control plants were sprayed in the same way with the complete solvent. [000187] The treated plants and the control plants were placed in a greenhouse as described above and watered by sub-irrigation to prevent washing extraction of the test compounds. After approximately 3 weeks, the condition of the test plants when compared to the condition of the untreated plants was visually determined and rated on a scale of 0 to 100 percent where 0 corresponds to no injury or growth inhibition and 100 corresponds to complete killing. [000188] Colby's equation was used to determine the expected herbicidal effects of the mixtures (Colby, S.R. 1967. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 15: 20-22.). [000189] The following equation was used to calculate the expected activity of mixtures containing two active ingredients, A and B: Expected = A + B - (A x B / 100) A = observed effectiveness of active ingredient A at the same concentration as used in the mix. B = observed effectiveness of active ingredient B at the same concentration as used in the mixture. [000190] The tested compounds, the application rates employed, the plant species tested, and the results are provided in Tables 1 to 21. Table 1. Synergistic Activity of Herbicidal Compositions of Acid and Cialofop-Butyl Compound A Applied in Leaves on Weed Control in a Rice Culture System. Table 2. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Cialofop-Butyl Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 3. Synergistic Activity of Herbicidal Compositions of Acid and Fenoxprop-p-ethyl + Isoxadifen-ethyl of Compound A Applied to Leaves on the Control of Weeds in a Rice Culture System. * g ia / ha refers to the concentration of phenoxaprop-p-ethyl Table 4. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Fenoxaprop-p-ethyl + Isoxadifen-ethyl of Compound A Applied to Leaves on Weed Control in a Rice Culture System. * g ia / ha refers to the concentration of phenoxaprop-p-ethyl Table 5. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Fenoxaprop-p-ethyl + Mefenpir-diethyl Compound A Applied to Leaves on Weed Control in Systems of Rice Culture. * g ia / ha refers to the concentration of phenoxaprop-p-ethyl Table 6. Synergistic Activity of Herbicidal Compositions of Acid and Haloxifop-methyl of Compound A Applied in Leaves on the Control of Common Weeds in Rice Culture Systems. Table 7. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Haloxifop-Methyl Compound A Applied in Leaves on the Control of Common Weeds in Rice Culture Systems. Table 8. Synergistic Activity of Herbicidal Compositions of Acid and Metamifop of Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 9. Synergistic Activity of Herbicidal Compositions Benzyl Ester and Metamifop of Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 10. Synergistic Activity of Herbicidal Compositions of Acid and Fluazifop-p-butyl of Compound A Applied to Leaves on the Control of Common Weeds in Rice Culture Systems. Table 11. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Fluazifop-p-butyl Compound A Applied in Leaves on the Control of Common Weeds in Rice Culture Systems. Table 12. Synergistic Activity of Herbicidal Compositions of Acid and Quizalofop-p-ethyl of Compound A Applied in Leaves on the Control of Common Weeds in Rice Culture Systems. Table 13. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Quizalofop-Ethyl Compound A Applied to Leaves on the Control of Common Weeds in Rice Culture Systems. Table 14. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Diclofop-Methyl Compound A Applied in Leaves on the Control of Common Weeds in Rice Culture Systems. Table 15. Synergistic Activity of Herbicidal Compositions of Acid and Profoxidim of Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 16. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Profoxidim of Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 17. Synergistic Activity of Compound A Acid and Setoxidim Herbicidal Compositions Applied to Leaves on Common Weed Control in Rice Culture Systems. Table 18. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Setoxidim of Compound A Applied in Leaves on the Control of Common Weeds in Rice Culture Systems. Table 19. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Tralcoxidim of Compound A Applied in Leaves on the Control of Common Weeds in Rice Culture Systems. Table 20. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Pinoxaden of Compound A Applied in Leaves on the Control of Common Weeds in Rice Culture Systems. Table 21. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Cletodim of Compound A Applied in Leaves on the Control of Common Weeds in Rice Culture Systems. BRAPP Brachia ria platyphylla (Griseb.) Nash brachiaria, hardwood CYPDI Cyperus difformis L. june, umbrella CYPES Cyperus esculentus L. juniper CYPIR Cyperus would L. flat junction, rice DIGSA Digitaria sanguinalis (L.) Scop. large, ECHCG Echinochloa crusgalli (L.) Beauv. ECHCO grass Echinochloa colona (L.) Link junglerice IPOHE Ipomoea hederacea Jacq. morning glory, ISCRU ivy Ischaemum rugosum Salisb. saramollagrass LEFCH Leptochloa chinensis (L.) Nees sprangletop, Chinese SCPJU SchoenoplectusJuncoides (Roxb.) Palia reed, Japanese g ea / ha = grams of acid equivalent per hectare g ia / ha = grams of active ingredient per hectare Obs = observed value Exp = expected value as calculated by the Colby equation DAA = days after application NT = not tested Example II. Evaluation of Herbicidal Mixtures Applied in Water for Weed Control in Transplanted Paddy Rice [000191] Small weed seeds or nuts of the desired test plant species were planted in pond (mud) soil prepared by mixing a fragmented non-sterile mineral soil (50.5 percent sludge, 25.5 percent clay, and 24 percent sand, with a pH around 7.6 and an organic matter content around 2.9 percent) and water in a volumetric ratio of 1: 1. The prepared sludge was dispensed in 365 mL aliquots in 454 g (16 oz.) Unperforated plastic pots with a surface area of 86.59 square centimeters (cm2) leaving a free top of 3 centimeters (cm) ) in each pot. The sludge was allowed to dry overnight before planting or transplanting. The rice seeds were planted in the plantation mixture in Sun Gro MetMix®, which typically has a pH of 6.0 to 6.8 and an organic matter content of around 30 percent, in trays with a plastic lid . The seedlings in the second or third stage of leaf growth were transplanted in 860 mL of mud contained in 907g (32-oz.) Unperforated plastic pots with a surface area of 86.59 cm2 4 days before herbicide application. The rice was created by loading the free top of the pots with 2.5 to 3 cm of water. When required to ensure good germination and healthy plants, a fungicide treatment and / or other chemical or physical treatment was applied. The plants were grown for 4 to 22 days in a greenhouse with a photoperiod of approximately 14 h which was kept at around 29 ° C during the day and 26 ° C at night. The nutrients were added as Osmocote® (19: 6: 12, N: P: K + secondary nutrients) in a pot of 2 g per 454 g (16-oz.) And a pot of 4 g per 907 g (32-oz. ) Water was added on a regular basis to keep the rice from flooding, and supplementary lighting was provided with 1000 Watt metal halide suspended lamps as needed. The plants were used for testing when they reached the first to the fourth authentic leaf stage. [000192] The treatments consisted of 4- amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxy-phenyl) pyridine-2-carboxylic acid or esters (compound A) each Formulated as a SC (suspension concentrate) and various herbicide components alone and in combination. Compound A forms were applied on an equivalent acid base. [000193] The forms of compound A (compound of Formula I) tested include: Compound A Acid Benzyl Ester of Compound A [000194] Other herbicidal components were applied on an acid equivalent (ae) or active ingredient (ai) basis as for normal commercial practice, and included acetyl CoA carboxylase (ACCase) inhibiting herbicides (chemical classes) cyclohexanedione and aryloxyphenoxypropionate) cialofop-butyl formulated as Clincher® EC, phenoxaprop-p-ethyl + isoxadifen-ethyl formulated as RiceStar® HT, phenoxaprop-p-ethyl + mefenpir diethyl formulated as Puma 1EC, metamifop formulated as Metamifop EC, haloxifop-methyl formulated as Gallant Super®, fluazifop-p-butyl formulated as Fusilade® DX, quizalofop-p-ethyl formulated as Assure® II, profoxidim formulated as Aura® 20EC, and setoxidim formulated as Po-ast®. [000195] The treatment requirements for each compound or herbicidal component were calculated based on the rates being tested, the concentration of active ingredient or acid equivalent in the formulation, an application volume of 2 mL per component per pot, and a application area of 86.59 cm2 per pot. [000196] For the formulated compounds, a measured quantity was placed in a 100 or 200 mL individual glass bottle and was dissolved in a volume of 1.25% (v / v) of Agricola oil concentrate Dex® for application solutions. If the test compound does not dissolve easily, the mixture is heated and / or subjected to ultrasound. [000197] For technical grade compounds, a weighted amount can be placed in an individual 100 or 200 mL glass bottle and dissolved in a volume of acetone to obtain concentrated raw material solutions. If the test compound does not dissolve easily, the mixture can be heated and / or subjected to ultrasound. The concentrated raw material solutions obtained can be diluted with an equivalent volume of an aqueous mixture containing 2.5% (v / v) of culture oil concentrate so that final application solutions contain 1.25% (v / v) of culture oil concentrate. [000198] The applications were prepared by injecting an appropriate amount of pipette of the application solutions, individually and sequentially, into the aqueous layer of the rice field. The control plants were treated the same way as the complete solvent. The applications were prepared so that all the treated plant material receives the same concentrations of acetone and culture oil concentrate. [000199] The treated plants and the control plants were placed in a greenhouse as described above and water was added when necessary to maintain a flood of rice. After approximately 3 weeks the condition of the test plants when compared to the condition of the untreated plants was visually determined and rated on a scale of 0 to 100 percent where 0 corresponds to no injury or growth inhibition and 100 corresponds to complete killing. [000200] Colby's equation was used to determine the expected herbicidal effects of the mixtures (Colby, S.R. 1967. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 15: 20-22.). [000201] The following equation was used to calculate the expected activity of mixtures containing two active ingredients, A and B: Expected = A + B - (A x B / 100) A = observed effectiveness of active ingredient A at the same concentration as used in the mix. B = observed effectiveness of active ingredient B at the same concentration as used in the mixture. [000202] Some of the tested compounds, application rates employed, tested plant species, and results are provided in Tables 22 to 39. Table 22. Synergistic Activity of Water Applications of Compound A Acid and Cialofop-butyl Compounds on o Weed Control in a Rice Culture System. Table 23. Synergistic Activity of Water Applications of Compound A Benzyl Ester and Cialofop-Butyl Herbicide Compositions on Weed Control in a Rice Culture System. Table 24. Synergistic Activity of Water Applications of Herbicidal Compositions of Acid and Fenoxaprop-p-ethyl + Isoxadifen-ethyl of Compound A on the Control of Weeds in a Rice Culture System. Table 25. Synergistic Activity of Water Applications of Herbicidal Compositions of Benzyl Ester and Fenoxaprop-p-ethyl + Isoxadiphenyl of Compound A on Weed Control in a Rice Culture System. Table 26. Synergistic Activity of Water Applications of Herbicidal Compositions of Acid and Fenoxaprop-p-ethyl + Mefenpir-diethyl of Compound A on the Control of Common Weeds in Rice Culture Systems. Table 27. Synergistic Activity of Water Applications of Herbicidal Compositions of Benzyl Ester and Fenoxaprop-p-ethyl + Mefenpirethyl Diethyl Compound A on the Control of Common Weeds in Rice Culture Systems. Table 28. Synergistic Activity of Water Applications of Compound A Acid and Haloxifop-Butyl Compositions on the Control of Common Weeds in Rice Culture Systems. Table 29. Synergistic Activity of Water Applications of Compound A Benzyl Ester and Haloxifop-Methyl Herbicidal Compositions on the Control of Common Weeds in Rice Culture Systems. Table 30. Synergistic Activity of Water Applications of Herbicidal Compositions of Acid and Metamifop of Compound A on Weed Control in a Rice Culture System. Table 31. Synergistic Activity of Water Applications of Herbicidal Compositions of Benzyl Ester and Metamitop of Compound A on Weed Control in a Rice Culture System. Table 32. Synergistic Activity of Water Applications of Compound A Acid and Fluazifop-p-butyl Compositions on the Control of Common Weeds in Rice Culture Systems. Table 33. Synergistic Activity of Water Applications of Herbicidal Compositions of Benzyl Ester and Fluazifop-p-butyl of Compound A on the Control of Common Weeds in Rice Culture Systems. Table 34. Synergistic Activity of Water Applications of Compound A Acid and Quizalofop-p-Ethyl Compositions on the Control of Common Weeds in Rice Culture Systems. Table 35. Synergistic Activity of Water Applications of Compound A Benzyl Ester and Quizalofop-p-Ethyl Compositions on the Control of Common Weeds in Rice Culture Systems. Table 36. Synergistic Activity of Water Applications of Herbicidal Compositions of Acid and Profoxidim of Compound A on the Control of Common Weeds in Rice Culture Systems. Table 37. Synergistic Activity of Water Applications of Herbicidal Compositions of Benzyl Ester and Profoxidim of Compound A on the Control of Common Weeds in Rice Culture Systems. Table 38. Synergistic Activity of Water Applications of Compound A Acid and Setoxidim Herbicidal Compositions on the Control of Common Weeds in Rice Culture Systems. Table 39. Synergistic Activity of Water Applications of Herbicidal Compositions of Benzyl Ester and Setoxidim of Compound A on the Control of Common Weeds in Rice Culture Systems. CYPRO Cyperus rotundus L. tiririca ECHCG Echinochloa crusgalli (L.) Beauv. ECHOR grass Echinochloa oryzoides (Ard.) Fritsch early water grass FIMMI Fimbristylis miliacea (L.) Vahl fringerush, globe LEFCH Leptochloa chinensis (L.) Nees sprangletop, Chinese SCPJU Schoenoplectus juncoides (Roxb.) L.) Palia or Schoenoplectus maritimus (L.) Lye clubrush, sea g ea / ha = grams of acid equivalent per hectare g ia / ha = grams of active ingredient per hectare Obs = observed value Exp = expected value as calculated by the equation Colby DAA = days after application Example III. Evaluation of Herbicidal Mixtures Applied to Post-emergence Leaves for the Control of Common Weeds in Serial Crops such as Corn and Soybeans [000203] Seeds or small nuts of the desired test plant species were planted in a soil matrix prepared by mixing a clay or sandy clay soil (eg 28.6 percent sludge, 18.8 percent clay, and 52.6 percent sand, with a pH around 5.8 and an organic matter content around 1.8 percent) and limestone sand in a ratio of 80 to 20. The soil matrix was contained in pots of plastic with a surface area of 84.6 square centimeters (cm2) and a volume of 560 cubic centimeters (cm3). When required to ensure good germination and healthy plants, a fungicide treatment and / or other chemical or physical treatment was applied. The plants were grown for 7 to 31 days (d) in a greenhouse with a photoperiod of approximately 15 hours (h) which was maintained at around 23 to 29 ° C during the day and from 22 to 28 ° C at night . Nutrients (Peters Excel® 15-5-15 5-Ca 2-Mg) and water were added on a regular basis and supplementary lighting was provided with 1000 Watt metal halide suspended lamps as needed. The plants were used for testing when they reached the first, second or third authentic leaf stage. [000204] The treatment requirements were calculated based on the rates being tested, the concentration of active ingredient or acid equivalent in the formulation, and an application volume of 12 mL at a rate of 187 L / ha. [000205] The treatments consisted of 4- amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxy-phenyl) pyridine-2-carboxylic acid or esters (Compound A) , each formulated as a SC (suspension concentrate), and various herbicidal components alone and in combination. Compound A forms were applied on an equivalent acid base. [000206] The forms of compound A (compound of Formula I) tested include: Benzyl Ester of Compound A [000207] Other herbicidal components were applied on an equivalent acid base and included the acetyl coA carboxylase (ACCase) inhibiting herbicide (classes of chemical cyclohexanedione and aryloxyphenoxypropionate) quizalofop-p-ethyl formulated as Assure® II. [000208] For treatments comprised of formulated compounds, measured amounts of compounds were placed individually in 25 ml glass bottles and diluted in a volume of 1.5% (v / v) of concentrated Agri-Dex® culture oil for obtain 6X raw material solutions. If a test compound does not dissolve easily, the mixture is heated and / or subjected to ultrasound. The application solutions were prepared by adding an appropriate amount of each raw material solution (typically 2 ml) and diluted to the appropriate final concentrations with the addition of an appropriate amount of 1.5% (v / v) concentrate. culture oil and an appropriate amount of water so that the final spray solutions contain 1.25 +/- 0.05% (v / v) of culture oil concentrate. [000209] For treatments comprised of technical compounds, weighted amounts can be placed individually in 25 ml_ glass bottles and dissolved in a 97: 3 v / v acetone / DMSO volume to obtain 12X raw material solutions. If a test compound does not dissolve easily, the mixture can be heated and / or subjected to ultrasound. Application solutions can be prepared by adding an appropriate amount of each raw material solution (for example, 1 ml) and diluted to the appropriate final concentrations with the addition of an appropriate amount of 1.5% ( v / v) culture oil concentrate and an appropriate amount of water so that the final spray solutions contain 1.25% (v / v) culture oil concentrate. When technical materials are used, concentrated raw material solutions can be added to the spray solutions so that the final concentrations of acetone and DMSO in the application solutions are 16.2% and 0.5%, respectively. [000210] For treatments comprised of formulated and technical compounds, weighted amounts of technical materials can be placed individually in 25 ml_ glass vials and dissolved in a 97: 3 v / v acetone / DMSO volume to obtain raw material solutions press 6X, and measured amounts of formulated compounds can be placed individually in 25 ml_ glass bottles and diluted in a volume of 1.5% (v / v) of culture oil concentrate or water to obtain raw material solutions 6X. If a test compound does not dissolve easily, the mixture can be heated and / or subjected to ultrasound. Application solutions can be prepared by adding an appropriate amount of each raw material solution (eg 2 ml) and diluted to the appropriate final concentrations with the addition of an appropriate amount of an aqueous mixture of 1 , 5% (v / v) of culture oil concentrate so that the final spray solutions contain 1.25% (v / v) of culture oil concentrate. When required, additional water and / or 97: 3 v / v acetone / DMSO can be added to the individual application solutions so that the final concentrations of acetone and DMSO of the application solutions being compared were 16.2% and 0, 5%, respectively. [000211] All raw material solutions and application solutions were visually inspected for compound compatibility prior to application. The compost requirements are based on an application volume of 12 mL at a rate of 187 liters per hectare (L / ha). The formulated compounds were applied to the plant material with a Mandei suspended chute sprayer equipped with a 8002E nozzle calibrated to release 187 L / ha over an application area of 0.503 square meters (m2) at a spray height of 46 to 50 cm (18 20 inches) above the average canopy height of the plant. The control plants were sprayed in the same way with the complete solvent. [000212] The treated plants and the control plants were placed in a greenhouse as described above and watered by sub-irrigation to prevent washing extraction of the test compounds. After approximately 2 weeks, the condition of the test plants when compared to the condition of the untreated plants was determined visually and rated on a scale of 0 to 100 percent where 0 corresponds to no injury or growth inhibition and 100 cor-respond to killing complete. [000213] Colby's equation was used to determine the expected herbicidal effects of the mixtures (Colby, S.R. 1967. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 15: 20-22.). [000214] The following equation was used to calculate the expected activity of mixtures containing two active ingredients, A and B: Expected = A + B - (A x B / 100) A = observed effectiveness of active ingredient A at the same concentration as used in the mix. B = observed effectiveness of active ingredient B at the same concentration as used in the mixture. [000215] Some of the compounds tested, the application rates applied, the plant species tested, and the results are provided in Tables 40 to 41. Table 40. Synergistic Activity of Herbicidal Acid and Quizalofop-p-ethyl compositions of Compound A Applied to Leaves on Common Weed Control in Serial Crops such as Corn and Soy Culture Systems. Table 41. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Quizalofop-p-ethyl of Compound A Applied in Leaves on the Control of Common Weeds in Serial Crops such as Corn and Soy Culture Systems. AVEFA Avena fatua L. oats, silvesl tre LOLMU Lolium multiflorum Lam. Ryegrass, Italian g ea / ha = grams of acid equivalent per hectare g ia / ha = grams of active ingredient per hectare Obs = observed value Exp = expected value as calculated by the Colby DAA equation = days after application Example IV. Evaluation of Herbicidal Activity Post-emergence of Mixtures in Cereal Cultures in the Greenhouse. [000216] Seeds of the desired test plant species were planted in the Sun Gro MetroMix® planting mixture, which typically has a pH of 6.0 to 6.8 and an organic matter content of around 30 percent, in plastic pots with a surface area of 103.2 square centimeters (cm2). When required to ensure good germination and healthy plants, a fungicide treatment and / or other chemical or physical treatment was applied. The plants were grown for 7 to 36 days in a greenhouse with an approximate 14 hour photoperiod which was maintained at around 18 ° C during the day and around 17 ° C at night. Nutrients and water were added on a regular basis and supplementary lighting was provided with 1000 Watt metal halide hanging lamps as needed. The plants were used for testing when they reached the second or third authentic leaf stage. [000217] The treatments consisted of the benzyl ester of 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxy-phenyl) pyridine-2-carboxylic acid (Compound A), formulated as a SC, a second cereal herbicide alone and then in combination. [000218] The forms of compound A (compound of Formula I) tested include: Benzyl Ester of Compound A [000219] Other herbicidal components were applied on an active ingredient basis and included acetyl-CoA carboxylase (ACCase) inhibiting herbicides clodinafop-propargyl, phenoxaprop-P-ethyl, pinoxaden and tralcoxidim. [000220] Measured aliquots of 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxy-phenyl) pyridine-2-carboxylic acid benzyl ester (Compound A) in 25 milliliter (ml) glass bottles and diluted in a 1.25% (v / v) volume of Agri-Dex® culture oil concentrate to obtain raw material solutions. The compost requirements are based on an application volume of 12 mL at a rate of 187 liters per hectare (L / ha). The spray solutions of the second cereal herbicide and experimental compound mixtures were prepared by adding the raw material solutions in the appropriate amount of dilution solution to form 12 ml of spray solution with active ingredients in two- and three-way combinations. The formulated compounds were applied to the plant material with a Mandei suspended chute sprayer equipped with a 8002E nozzle calibrated to release 187 L / ha over an application area of 0.503 square meters (m2) at a spray height of 46 cm (18 inches) ) above the average canopy height of the plant. The control plants were sprayed in the same way with the complete solvent. [000221] The treated plants and the control plants were placed in a greenhouse as described above and watered by sub-irrigation to prevent washing extraction of the test compounds. After 20 to 22 days, the condition of the test plants when compared to the condition of the control plants was determined visually and rated on a scale of 0 to 100 percent where 0 corresponds to no injury and 100 corresponds to complete killing. [000222] Colby's equation was used to determine the expected herbicidal effects of the mixtures (Colby, S.R. 1967. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 15: 20-22.). [000223] The following equation was used to calculate the expected activity of mixtures containing two active ingredients, A and B: Expected = A + B - (A x B / 100) A = observed effectiveness of active ingredient A at the same concentration as used in the mix. B = observed effectiveness of active ingredient B at the same concentration as used in the mixture. [000224] The compounds tested, the rates of application employed, the plant species tested, and the results are provided in Tables 42 to 45. Table 42. Synergistic Activity of Herbicidal Compositions of Benzyzester Ester and Clodinafop-Propargyl of Compound A Applied to Leaves on Weed Control in a Cereal Culture System. Table 43. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Phenoxaprop-P-ethyl of Compound A Applied to Leaves on Weed Control in a Cereal Culture System. Table 44. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Pinoxaden of Compound A Applied to Leaves on Weed Control in a Cereal Culture System. Table 45. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Compound A Tralcoxidim Applied to Leaves on Weed Control in a Cereal Culture System. ALOMY Alopecurus myosuroides Huds. black grass APESV Apera spica-venti (L.) Beauv. wind grass AVEFA Avena fatua L. wild oats KCHSC Kochia scoparia (L.) Schrad. kochia LOLMU Lolium multiflorum Lam. PH AM I Phalaris minor Retz. ryegrass, Italian seedling, small seed g ea / ha = grams of acid equivalent per hectare g ia / ha = grams of active ingredient per hectare Obs = observed value Exp = expected value as calculated by the Colby equation DAA = days after application Example V. Post-emergence Herbicidal Activity Evaluation of Mixtures Applied under Field Conditions in Seeded Rice [000225] Multiple field experiments were conducted under the field conditions of commercial producers in Tolima, Colombia; Thessaloniki, Greece; Bianze and Copiano, Italy; and Humphrey, Arkansas, USA. The experiment sites were located in commercially developed areas of no-till rice (Oryza sativa) using the small batch research methodology with standard herbicide. The batches varied from 2 to 3 meters (m) x 5 to 8 m (width x length) with 4 replicates per treatment. The rice crop was developed using normal cropping practices during fertilization, seeding, irrigation, flooding and maintenance to ensure good growth of the crop and weeds. [000226] All treatments in the field experiments were applied using a backpack air / compressed gas sprayer with flat jet nozzles (80 ° or 110 °) calibrated to apply 187 to 300 L / ha of pressure spray volume nozzle of approximately 200 to 400 kPa. Commercially available cyhalofop-butyl products (Clincher 180EC, Clincher 200EC, and Clincher SF (285 gai / L EC)) were mixed in water at the appropriate formulated product rates to achieve the desired rates based on a unit area of application ( hectare) to achieve the desired rates as shown. Treatments were evaluated 19 to 58 days after application (DAA) compared to untreated control plants. Visual weed control was rated on a scale of 0 to 100 percent where 0 corresponds to no injury and 100 corresponds to complete killing. [000227] All treatment results, both for the isolated product and for the mixtures, are an average of 4 replicates. The test sites had populations of naturally occurring weeds. The weed spectrum included, but was not limited to, flat rice sedge (Cyperus vai, CYPIR); smallflower small flower umbrella plant (Cyperus difformis, CYPDI), jungle rice (Echinochloa colona, ECHCO), grass (Echinochloa crus-galli, ECHCG); multiple species of Echinochloa in the same field (ECHSS), grasslike fimbristylis (Fimbristylis miliacea, FIMMI); reed from the rice field (Schoenoplectus mucronatus, SCPMU) and Sesbania hemp (Sesbania exaltata, SEBEX). All synergistic interactions were significant at the P> 0.01 level. [000228] Some of the compounds tested, the application rates applied, the plant species tested, and the results are provided in Tables 46-48. Table 46. Synergistic Activity of Compound A Benzyl Ester and Cialofop-Butyl Herbicidal Compositions Applied to Leaves on Weed Control in a Rice Culture System when assessed 19 DAA (Days after application) in Tolima, Colombia. Table 47. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Cialofop-butyl Compound A Applied to Leaves on Weed Control in a Rice Culture System when 7DAA (Days after application) was evaluated in Humphrey, Arkansas, USA. Table 48. Synergistic Activity of Herbicidal Compositions of Benzyl Ester and Cialofop-butyl Compound A Applied to Leaves on Weed Control in a Rice Culture System when assessed at 55 to 58 DAA (Days after application) in Greece (CYPDI and ECHCG) and Italy (ECHSS and SCPMU). Example V. Evaluation of Ternary Herbicidal Mixtures Applied to Post-emergence Leaves for Weed Control in No-Till Rice [000229] Seeds or small nuts of the desired test plant species were planted in a soil matrix prepared by mixing a sandy clay or clay soil (for example, 32 percent mud, 23 percent clay, and 45 percent sand , with a pH around 6.5 and an organic matter content around 1.9 percent) and limestone sand in a ratio of 80 to 20. The soil matrix was contained in plastic pots with a volume of 1 liter (1 quarter gallon) and a surface area of 83.6 square centimeters (cm2). When required to ensure good germination and healthy plants, a fungicide and / or other chemical or physical treatment treatment was applied. The plants were grown for 8 to 22 days in a greenhouse with a photoperiod of approximately 14 h which was kept at around 29 ° C during the day and 26 ° C at night. The nutrients (Peters Excel® 15-5-15 5-Ca 2-Mg and iron chelate) were applied to the irrigation solution when necessary and water was added on a regular basis. Supplementary lighting was provided with 1000 Watt metal halide suspended lamps when needed. The plants were used for testing when they reached the first to the fourth authentic leaf stage. [000230] The treatments consisted of 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxy-phenyl) pyridine-2-carboxylic acid benzyl ester (Compound A), formulated as a SC (suspension concentrate), an ACCase inhibitor, and a third herbicidal component, each applied alone and in ternary combination. Compound A forms were applied on an equivalent acid base. [000231] The forms of compound A (compound of Formula I) tested include: Benzyl Ester of Compound A [000232] The ACCase inhibitor component was applied to an active ingredient base and included cyhalofop-R-butyl formulated as Clincher® SF, phenoxaprop-p-ethyl formulated as RiceStar® HT, and profoxi-dim formulated as Aura® 20EC. Other herbicidal components were applied over an active ingredient or equivalent acid base depending on the compound and included penoxsulam formulated as Grasp® SC, sodium bentazon formulated as Basagran®, triclopyr trimethylammonium salt (TEA) formulated as Grandstand® R, sodium bispiribac formulated as Regiment® 80WP, imazamox ammonium formulated as Beyond®, benzobicyclon, quinclorac formulated as Facet® 75DF, glyphosate dimethylammonium (DMA) salt formulated as Durango® DMA, glu-phosinate ammonium formulated as Ignite® 280, fentrazamide formulated as an emulsifiable concentrate ( EC), propirisulfuron formulated as Zeta One®, and indanofan (technical grade material). [000233] Treatment requirements were calculated based on the rates being tested, the concentration of active ingredient or acid equivalent in the formulation, and an application volume of 12 mL at a rate of 187 L / ha. [000234] For treatments comprised of formulated compounds, measured amounts of compounds were placed individually in 25 ml glass bottles and diluted in a volume of 1.25% (v / v) of Agri-Dex® culture oil concentrate to obtain 12X raw material solutions. If a test compound does not dissolve easily, the mixture is heated and / or subjected to ultrasound. The application solutions were prepared by adding an appropriate amount of each raw material solution (for example, 1 ml) and diluted to the appropriate final concentrations with the addition of 9 ml of a 1.25% (v / v) culture oil concentrate so that the final spray solutions contain 1.25% (v / v) culture oil concentrate. [000235] For treatments comprised of formulated and technical compounds, weighted amounts of the technical materials were placed individually in 25 ml glass bottles and dissolved in a 97: 3 v / v acetone / DMSO volume to obtain solutions of 12X raw material, and measured amounts of the formulated compounds were placed individually in 25 ml_ glass bottles and diluted in a 1.5% (v / v) volume of culture oil concentrate to obtain 12X raw material solutions . If a test compound does not dissolve easily, the mixture is heated and / or subjected to ultrasound. The application solutions were prepared by adding an appropriate amount of each raw material solution (for example, 1 ml) and diluted to the appropriate final concentrations with the addition of an appropriate amount of a 1.5% aqueous mixture (v / v) of culture oil concentrate so that the final spray solutions contain 1.25% (v / v) of culture oil concentrate. As required, additional water and / or 97: 3 v / v acetone / DMSO was added to the individual application solutions so that the final concentrations of acetone and DMSO of the application solutions being compared were 8.1% and 0.25% , respectively. [000236] All raw material solutions and application solutions were visually inspected for compatibility of the compound prior to application. The spraying solutions were applied to the plant material with a drop-out water spray from the Mandi equipped with an 8002E nozzle calibrated to release 187 L / ha over a 0.50 m2 application area at a spray height of 46 cm (18 inches) above average plant canopy height. The control plants were sprayed in the same way with the complete solvent. [000237] The treated plants and the control plants were placed in a greenhouse as described above and watered by sub-irrigation to prevent extraction by washing the test compound. After approximately 3 weeks, the condition of the test plants when compared to the condition of the untreated plants was visually determined and rated on a scale of 0 to 100 percent where 0 corresponds to no injury or growth inhibition and 100 cor-respond to killing complete. [000238] Colby's equation was used to determine the expected herbicidal effects of the mixtures (Colby, S.R. 1967. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 15: 20-22.). [000239] The following equation was used to calculate the expected activity of mixtures containing three active ingredients, A, B, and C: Expected = A + B + C - (((A xB + AxC + Bx C) / 100) + ( A x BxC / 10000) A = observed effectiveness of active ingredient A in the same concentration as used in the mixture. B = observed effectiveness of active ingredient B at the same concentration as used in the mixture. C = observed effectiveness of active ingredient C at the same concentration as used in the mixture. [000240] The tested compounds, the application rates employed, the plant species tested, and the results are provided in Tables 49 to 62. Table 49. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Penoxsulam of the Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 50. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Bentazon of Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 51. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Triclopir TEA salt of Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 52. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Bispiribac Sodium Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 53. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Imazamox Ammonium Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 54. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Benzobicyclon of Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 55. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Quinclorac of Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 56. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Glyphosate Dimethylammonium Salt (DMA) of Compound A Applied to Leaves on the Control of Weeds in a Rice Culture System. Table 57. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-Butyl and Compound A Ammonium Glufosinate Applied to Leaves on Weed Control in a Rice Culture System. Table 58. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Fentrazamide of Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 59. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Propirisulfuron of Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 60. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Fenoxaprop-p-ethyl + Isoxadifen-ethyl Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 61. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Profoxidim and Penoxsulam of Compound A Applied to Leaves on Weed Control in a Rice Culture System. Table 62. Synergistic Activity of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Indanofan of Compound A Applied to Leaves on Weed Control in a Rice Culture System. CYPES Cyperus esculentus junça CYPIR Cyperus would L. flat tiririca, ECHCG Echinochloa crusgalli (L.) Beauv rice. ECHCO grass Echinochloa colona (L.) Link jungle rice ECHOR Echinochloa oryzoides (Ard.) Fritsch grass from early waters IPOHE Ipomoea hederacea Jacq. ipomea, ivy LEFCH Leptochloa chinensis (L.) Nees sprangletop, Chinese SCPJU Schoenoplectus juncoides (Roxb.) Palia reed, Japanese g ea / ha = grams of acid equivalent per hectare g ia / ha = grams of active ingredient per hectare Obs = observed value Exp = expected value as calculated by the Colby equation DAA = days after application Example VI. Evaluation of Ternary Herbicidal Mixtures Applied in Water for the Control of Weeds in Transplanted Rice Paddies [000241] Seeds or small weed nuts of the desired test plant species were planted in pond (mud) soil prepared by mixing a fragmented non-sterile mineral soil (50.5 percent sludge, 25.5 percent clay, and 24 percent sand, with a pH around 7.6 and an organic matter content around 2.9 percent) and water in a volumetric ratio of 1: 1. The prepared sludge was dispensed in 365 mL aliquots in 454 g (16 oz.) Unperforated plastic pots with a surface area of 86.59 square centimeters (cm2) leaving a free top of 3 centimeters (cm) ) in each pot. The sludge was allowed to dry overnight before planting or transplanting. The rice seeds were planted in the plantation mixture in Sun Gro MetMix®, which typically has a pH of 6.0 to 6.8 and an organic matter content of around 30 percent, in trays with a plastic lid . The seedlings in the second or third stage of leaf growth were transplanted to 860 mL of mud contained in 907 g (32-oz.) Unperforated plastic pots with a surface area of 86.59 cm2 4 days before herbicide application . The rice was created by loading the free top of the pots with 2.5 to 3 cm of water. When required to ensure good germination and healthy plants, a fungicide and / or other chemical or physical treatment treatment was applied. The plants were grown for 4 to 22 days in a greenhouse with a photoperiod of approximately 14 h which was kept at around 29 ° C during the day and 26 ° C at night. Nutrients were added as Osmocote® (19: 6: 12, N: P: K + secondary nutrients) in 2 g per 454 g (16-oz.) Bowl and 4 g per 907 g (32-oz. ) of vase. Water was added on a regular basis to keep the rice from flooding, and supplementary lighting was provided with 1000 watt metal halide hanging lamps when needed. The plants were used for testing when they reached the first to the fourth authentic leaf stage. [000242] The treatments consisted of the benzyl ester of 4-amino-3-chloro-5-fluoro-6- (4-chloro-2-fluoro-3-methoxy-phenyl) pyridine-2-carboxylic acid (Compound A), formulated as a SC (suspension concentrate), an ACCase inhibitor herbicide, and a third herbicide component, each applied alone and in ternary combination. Compound A forms were applied on an equivalent acid base. [000243] The forms of compound A (compound of Formula I) tested include: Benzyl Ester of Compound A [000244] The ACCase inhibitor component was applied on an active ingredient basis and included cialofop-R-butyl formulated as Clincher® G and metamifop formulated as Metamifop EC. Other herbicidal components were applied on an active ingredient or acid equivalent basis depending on the compound and included penoxsulam formulated as Grasp® SC, sodium bentazon formulated as Basagran®, trichlopyr trimethylammonium (TEA) salt formulated as Grandstand® R, benzobicyclon formulated as Benzobicyclon, benfuroresate formulated as Full Slot® WG, piraclonil formulated as Pyraclon® Flowable, mefenacet (technical grade material), and pretilachlor (technical grade material). [000245] The treatment requirements for each compound or herbicidal component were calculated based on the rates being tested, the concentration of active ingredient or acid equivalent in the formulation, an application volume of 1 ml_ per component per pot, and a application area of 86.59 cm2 per pot. [000246] For the formulated compounds, a measured quantity was placed in a 100 or 200 ml_ individual glass vial and was dissolved in a volume of 1.25% (v / v) of Agri-culture oil concentrate Dex® for application solutions. If the test compound does not dissolve easily, the mixture is heated and / or subjected to ultrasound. [000247] For technical grade compounds, a weighted amount was placed in an individual 100 or 200 ml glass bottle and was dissolved in a volume of acetone to obtain concentrated raw material solutions. If the test compound does not dissolve easily, the mixture is heated and / or subjected to ultrasound. The concentrated raw material solutions obtained were diluted with an equivalent volume of an aqueous mixture containing 2.5% (v / v) of oil concentrate so that the final application solutions contain 1.25% (v / v) of culture oil concentrate. [000248] The applications were prepared by injection with an appropriate amount of pipette of the application solutions, in the aqueous layer of the rice field. Control plants were treated in the same way with the complete solvent. The applications were prepared so that all the treated plant material receives the same concentrations of acetone and culture oil concentrate. [000249] The treated plants and the control plants were placed in a greenhouse as described above and water was added when necessary to maintain a flood of rice. After approximately 3 weeks the condition of the test plants when compared to the condition of the untreated plants was visually determined and rated on a scale of 0 to 100 percent where 0 corresponds to no injury or growth inhibition and 100 corresponds to complete killing. [000250] Colby's equation was used to determine the expected herbicidal effects of the mixtures (Colby, S.R. 1967. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 15: 20-22.). [000251] The following equation was used to calculate the expected activity of mixtures containing three active ingredients, A, B, and C: Expected = A + B + C - (((A xB + AxC + Bx C) / 100) + ( A x B x C / 10000) A = observed effectiveness of active ingredient A in the same concentration as used in the mixture. B = observed effectiveness of active ingredient B at the same concentration as used in the mixture. C = observed effectiveness of active ingredient C at the same concentration as used in the mixture. [000252] The tested compounds, the application rates employed, the plant species tested, and the results are provided in Tables 63 to 71. Table 63. Synergistic Activity of Water Applications of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Penox-sulam from Compound A on Weed Control in a Rice Culture System. Table 64. Synergistic Activity of Water Applications of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-Butyl and Triclopyr Trimethylammonium Salt of Compound A on Weed Control in a Rice Culture System. Table 65. Synergistic Activity of Water Applications of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-Butyl and Triclopyr Trimethylammonium Salt of Compound A on Weed Control in a Rice Culture System. Table 66. Synergistic Activity of Water Applications of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Compound A Beneficial on Weed Control in a Rice Culture System. Table 67. Synergistic Activity of Water Applications of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Benzobicyclon of Compound A on Weed Control in a Rice Culture System. Table 68. Synergistic Activity of Water Applications of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Pi-raclonil of Compound A on the Control of Weeds in a Rice Culture System. Table 69. Synergistic Activity of Water Applications of Ternary Herbicidal Compositions of Benzyl Ester, Cialofop-butyl and Mefenacet of Compound A on Weed Control in a Rice Culture System. Table 70. Synergistic Activity of Applications in Water of Benzyl Ester, Cialofop-butyl, and Pretilachlor of Compound A. Table 71. Synergistic Activity of Water Applications of Ternary Herbicidal Compositions of Benzyl Ester, Metamifop and Penoxsulfone of Compound A on Weed Control in a Rice Culture System. CYPRO Cyperus rotundus L. tiririca ECHCG Echinochloa crusgalli (L.) Beauv. ECHOR grass Echinochloa oryzoides (Ard.) Fritsch water grass, early FIMMI Fimbristylis miliacea (L.) Vahl fringerush, globe SCPJU Schoenoplectus juncoides (Roxb.) Palia junco, Japanese SCPMA Bolboschoenus maritimus (L.) Palla or Schoeno ) Lie clubrush, sea g ea / ha = grams of acid equivalent per hectare g ia / ha = grams of active ingredient per hectare Obs = observed value Exp = expected value as calculated by the Colby equation DAA = days after application
权利要求:
Claims (10) [0001] 1. Synergistic herbicidal composition, characterized by the fact that it comprises a herbicidally effective amount of: (a) a compound of Formula (I) [0002] 2. Composition, according to claim 1, characterized by the fact that it also comprises an agriculturally acceptable adjuvant or vehicle. [0003] 3. Composition according to claim 1 or 2, characterized by the fact that it also comprises a herbicide protector. [0004] 4. Composition according to any one of claims 1 to 3, characterized by the fact that it further comprises a compound selected from the group consisting of penoxsulam, bentazon-sodium, triclopyr, bispiribac-sodium, imazamox, benzobicyclone, quinclorac, glyphosphate, glufosinate, phenoxaprop-p-ethyl, isoxadifen-ethyl, profoxidim, benfuresate, fentrazamide, indanofan, mefenacet, pretilachlor, propyrisulfuron, pyraclonil and metamifop, or a carboxyl acid or salt . [0005] 5. Method for controlling undesirable vegetation, characterized by the fact that it comprises the steps of: contacting a plant, the plant being an undesirable vegetation, or its location, soil or water, being the soil or water they allow the growth of undesirable vegetation, with a herbicidally effective amount of a composition, as defined in any one of claims 1 to 4. [0006] 6. Method according to claim 5, characterized by the fact that undesirable vegetation is controlled in rice, cereals, wheat, barley, oats, rye, sorghum, corn, sugar cane, sunflower, rapeseed, canola, beet, soy, cotton, pineapple, pasture, lawn, pasture, abandoned land, peat, trees and vines, aquatic, industrial vegetation management (IVM) or easements (ROW) sown by no-tillage, water planting or transplanted. [0007] 7. Method according to claim 5 or 6, characterized by the fact that (a) and (b) are applied pre-emergently to the plant or crop. [0008] Method according to any one of claims 5 to 7, characterized by the fact that undesirable vegetation is controlled in glyphosate-tolerant cultures, 5-enolpyruvylchiquimate-3-phosphate (EPSP) synthase inhibitor, glufosinate, inhibitor of glutamine synthase, dicamba, phenoxy auxin, pyridyloxy auxin, synthetic auxin, auxin transport inhibitor, aryloxyphenoxypropionate, cyclohexanedione, phenylpyrazoline, acetyl CoA carboxylase inhibitor (ACCase), imidazolinone, sulfonyl-amine, tridimidine, tridimidine na, sulfonylaminocarbonyltriazolinone, acetolactate synthase (ALS) inhibitors or acetohydroxy acid synthase (AHAS), 4-hydroxyphenylpyruvate dioxigenase (HPPD) inhibitor, phyteno desaturase inhibitor, carotenoid biosynthesis inhibitor, protoporin inhibitor ), cellulose biosynthesis inhibitor, mitosis inhibitor, microtubule inhibitor, very long chain fatty acid inhibitor, bi inhibitor ossynthesis of fatty acid and lipid, inhibitor of photosystem I, inhibitor of photosystem II, triazine or bromoxynil. [0009] 9. Method, according to claim 8, characterized by the fact that the tolerant culture has multiple strains or strains piled up that confer tolerance to multiple herbicides or multiple modes of action. [0010] Method according to any one of claims 5 to 9, characterized in that the undesirable vegetation comprises a herbicide resistant or tolerant plant.
类似技术:
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同族专利:
公开号 | 公开日 SG11201500535SA|2015-02-27| PT2877017T|2020-02-14| SA115360515B1|2016-04-14| PH12015500151B1|2015-03-16| JP2015527334A|2015-09-17| ZA201501138B|2016-07-27| IL236850A|2020-02-27| EP2877017A4|2016-03-16| US8796177B2|2014-08-05| TWI655904B|2019-04-11| PE20150901A1|2015-05-31| AU2013293254A1|2015-03-05| UY34928A|2014-02-28| RU2015105995A|2016-09-10| US20150189879A1|2015-07-09| IN2015DN01375A|2015-07-03| JP6255399B2|2017-12-27| CN104661524B|2018-09-25| CA2879970A1|2014-01-30| US9232796B2|2016-01-12| WO2014018407A9|2014-05-30| PH12015500151A1|2015-03-16| MX2015001153A|2015-09-08| RU2632491C2|2017-10-05| HUE043811T2|2019-09-30| IL236850D0|2015-03-31| CL2015000187A1|2015-04-24| SA113340757B1|2015-07-07| EP2877017B1|2019-01-02| US20140031228A1|2014-01-30| BR102013018472A2|2015-02-18| ES2717034T3|2019-06-18| TW201406289A|2014-02-16| CN104661524A|2015-05-27| EP2877017A1|2015-06-03| CO7200279A2|2015-02-27| KR102104869B1|2020-04-29| PL2877017T3|2019-07-31| UA114917C2|2017-08-28| HK1210385A1|2016-04-22| WO2014018407A1|2014-01-30| AR091880A1|2015-03-04| AU2013293254B2|2017-04-13| KR20150038242A|2015-04-08|
引用文献:
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法律状态:
2015-02-17| B03A| Publication of a patent application or of a certificate of addition of invention [chapter 3.1 patent gazette]| 2015-04-14| B03H| Publication of an application: rectification [chapter 3.8 patent gazette]|Free format text: REFERENTE A RPI 2302 DE 18/02/2015, QUANTO AO ITEM (57). | 2016-10-11| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]| 2018-09-25| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]| 2019-03-12| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]| 2019-12-10| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]| 2020-04-07| B06A| Patent application procedure suspended [chapter 6.1 patent gazette]| 2020-07-07| B09A| Decision: intention to grant [chapter 9.1 patent gazette]| 2020-11-17| B16A| Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 19/07/2013, OBSERVADAS AS CONDICOES LEGAIS. |
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申请号 | 申请日 | 专利标题 US201261675103P| true| 2012-07-24|2012-07-24| US61/675,103|2012-07-24| US13/839,043|US8796177B2|2012-07-24|2013-03-15|Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-pyridine-2-carboxylic acid or a derivative thereof and acetyl-CoA carboxylaseinhibitors| US13/839,043|2013-03-15| 相关专利
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