• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
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  • 优先权
    • 专利摘要:
    A non-aqueous and stable concentrated single phase sleep developing agent (SO) formulation. The SO formulation comprises the compound of formula (I) and at least one vegetable oil and a polar aprotic organic solvent which are active ingredients. Also optionally, the SO formulation may have one or more methylated vegetable oils. SO preparations are useful as blast fungicides in aquatic environments of rice. <Formula I>
    公开号:KR20020059748A
    申请号:KR1020027006347
    申请日:2000-11-16
    公开日:2002-07-13
    发明作者:미하엘 아펜；히다에끼 하스이；마사또시 모또요시
    申请人:스타르크, 카르크；바스프 악티엔게젤샤프트；
    IPC主号:
    专利说明:

    Non-Aqueous Concentrated Spreading Oil Composition
    [1] The present invention relates to a spreading oil (SO) composition for crop protection active ingredients having a non-aqueous stable shelf life and its use for pest control, in particular in aquatic environments.
    [2] Until now, however, pesticides have usually been applied to paddy fields in the form of soluble, dispersible or absorbent granules which release the active ingredient in water or infusions, in particular in the form of emulsion formulations which disperse the active ingredient in the water (eg EP 0 206 987).
    [3] European patent application EP 0 415 569 discloses solid carriers for application in the aquatic environment, azocistrobin (the bactericide as active ingredient EP 0 382 375) and oils which can be mixed or dispersed with the active ingredient. A fungicidal composition comprising was proposed.
    [4] It is well known that the efficacy of plant protection agents is higher when the active ingredient is applied in dissolved form than when in particle form. One environmentally friendly way of applying the active ingredient in dissolved form is to dissolve it in vegetable oil. However, most plant protection agents do not show high solubility in vegetable oils.
    [5] In view of the need for easy and safe operation and the improvement of the efficacy of the plant protection agent, there is a need for the development of SO formulations for application to rice fields containing relatively high concentrations of the plant protection agent in the sleeping development agent.
    [6] <Overview of invention>
    [7] The present invention provides for the application of crop protection active compounds in aquatic environments,
    [8] 15 15 to 400 g / L of one or more crop protection active compounds;
    [9] 300 300 to 700 g / L of one or more vegetable oils;
    [10] 30 30 to 200 g / L of one or more polar aprotic organic solvents;
    [11] ⒟ optionally at least one methylated vegetable oil
    [12] It relates to a single phase non-aqueous concentrated sleep developing agent (SO) comprising the sum of all components in the formulation in a total of 1 liter. Another aspect of the invention is a method of making this SO formulation.
    [13] In addition, the present invention treats the SO formulation of the present invention in water in an aquatic environment, as a result of which the oil film spreads on the water surface and comes into contact with the plant (plants grown or grown in this aquatic environment containing the active ingredient before or later). The present invention relates to a method for controlling plant diseases and / or pests, including causing them to do so.
    [14] Another aspect of the invention
    [15] (Iii) at least one vegetable oil,
    [16] (Ii) at least one polar aprotic organic solvent; And
    [17] (Iii) optionally at least one methylated vegetable oil
    [18] Fungicidal triazolopyrimidine (e.g. EP 0550 113), particularly for the control of pests of rice plants, comprising the application of an effective amount of at least one compound of formula (I) dissolved in a mixture comprising A method of enhancing the potency of a compound of formula (I).
    [19]
    [20] These and other objects and features of the present invention will become more apparent from the detailed description set forth below.
    [21] For the application of crop protection active compounds in aquatic environments surprisingly,
    [22] 15 15 to 400 g / L of one or more crop protection active ingredients;
    [23] 300 300 to 700 g / L of one or more vegetable oils;
    [24] 30 30 to 200 g / L of one or more polar aprotic organic solvents;
    [25] ⒟ optionally at least one methylated vegetable oil
    [26] It has been found that stable single phase non-aqueous SO formulations can be obtained comprising the sum of all components in the formulation in a total of 1 liter.
    [27] The use of SO formulations can further increase the biological activity of the active ingredient controlling pests, as compared to conventional formulations.
    [28] The term single phase as used above and below means that the crop protection active compound V is completely dissolved in the homogeneous mixture of V, V, V and optionally V without phase separation.
    [29] The term pest as used above and below includes vegetable pathogens, insects and weeds.
    [30] In principle, all crop protection active compounds can be used in the preparation of non-aqueous concentrated sleep developing agents according to the invention. Preference is given to lipophilic crop protection active compounds.
    [31] Crop protection active compounds are usually used which are virtually insoluble in water and sub-solubility in pure vegetable oils. Solubility of less than 100 g / L, in particular of less than 50 g / L, in pure solvents is preferred.
    [32] The composition of the present invention can be applied to the aquatic environment of plants with other active substances. The active substances are to provide trace elements or other preparations which affect the beneficial microorganisms that are used to improve nutrition of the plant, such as growth or azepin Sat bakteo of plants (Azetobacter), separation tank via (Rhizobia) or sub Jolla (azolla) It may be a fertilizer or a drug. However, the active substances are preferably herbicides, insecticides, fungicides, fungicides, nematicides, acaricides, chelators, rodenticides, virus killers, compounds which induce resistance of plants, viruses, bacteria, nematodes, fungi and Biological inhibitors such as other microorganisms, algae and mammalian repellents and plant growth regulators, or mixtures of some of these preparations.
    [33] Preference is given to chemical crop protection compounds which are solid at room temperature, in particular having a melting point of at least 50 ° C.
    [34] Mixtures of several biologically active compounds may have a broader activity spectrum than when only one compound is present. The mixture can also produce synergistic effects when compared to the active ingredient alone. In a preferred embodiment, the formulations of the invention can be used in a mixture of active ingredients. In the case of mixtures, all active ingredients VII are dissolved in the solvent mixture of the SO formulations of the invention.
    [35] Preferred fungicides used in the compositions of the present invention are commercially available compounds selected from the group consisting of:
    [36] AC 382042, anilazine, azoxystrobin, benalacyl, benomil, vinapacryl, bitteranol, blasticidin S, bromuconazole, burimate, cappafol, captan, carbendazim, carboxycin, Carpropamide, chlorbenzthiazone, chlorothalonil, clozolinate, cycloheximide, simoxanyl, sipofuram, ciproconazole, ciprodinyl, diclofloanide, diclones, dichloran, Diclobutrazole, Diclocimet, Diclomezine, Dietofenecarb, Diphenocazole, Diflumethorim, Dimethymolol, Dimethomorph, Diconazole, Dinocap, Ditalimfoss, Dithianon , Dodemorph, dodyne, edifeneforce, emoxiconazole, etaconazole, etirimole, erythrazole, pamosadon, phenanilyl, phenamidone, phenarimol, fenbuconazole, fenfuram, phenhexa Mead, fenpiclonyl, fenpropidine, fenpropormoff, fentin, fentin acetate, perimzone, Luazin, fludioxonyl, flumetober, fluquinconazole, flusilazole, flusulfamid, flutolanil, flutriafol, polpet, fuberidazole, furalaxyl, furamepyr, guaztine , Hexaconazole, IKF-916, imazalyl, iminottadine, ifconazole, iprodione, isoprothiolane, iprovalicarb, kasugamycin, KH-7281, chitazine P, cresoxime-methyl, Mepanipyrim, mepronyl, metallaxyl, metconazole, metfuroxam, MON 65500, myclobutanyl, neoazin, nickel dimethyldithiocarbamate, nitrothalysopropyl, noarimol, opurais , Organic mercury compounds, oxadixyl, oxycarboxycin, fenconazole, penicuron, phenazine oxide, phthalide, polyoxin D, polylam, probenazole, prochloraz, procimidion, propamocarb, Propiconazole, propineb, pyrazophos, pyrifenox, pyrimethanyl, pyroquilon, pirox Fur, quinomethionate, quinoxyphene, quintogen, spiroxamine, SSF-126, SSF-129, streptomycin, tebuconazole, teclophthalam, technazen, tetraconazole, thibendazole, tiflu Zamide, thiophanate-methyl, thiram, toclofomethylmethyl, tolifluanide, triadimefon, triadimenol, triazbutyl, triazoxide, tricyclazole, tridemorph, tripleoxystrobin , Triflumizol, tripolin, triticazole, validamycin A, vinclozoline, XRD-563, zarylamide.
    [37] In addition, the preparations according to the invention may comprise one or more compounds of biological control agents, such as viruses, bacteria, nematodes, fungi and other microorganisms, which are suitable for controlling insects, weeds or plant diseases or inducing host resistance of plants. have. Examples of such biocontrol agents are as follows; Bacillus thuringiensis , Verticillium lecanii , Autographica californica NPV, Beauvaria bassiana , Ampelomyces quisqualis quisqualis , Bacilis subtilis , Pseudomonas Fluorescens , Streptomyces griseoviridis and Trichoderma harzianum .
    [38] In addition, the preparations according to the invention may be used in combination with one or more of the compounds which induce the required resistance throughout the plant, for example isonicicotinic acid or derivatives thereof, 2,2-dichloro-3,3, -dimethylcyclopropylcarboxylic acid or BION. And chemical agents.
    [39] Preferably the SO preparation comprises in particular derivatives of azolopyrimidines of the general formula (I), for example described in European patent application EP 0 550 113 or international patent application WO 98/46608.
    [40] <Formula I>
    [41]
    [42] Wherein R 1 and R 2 are each independently hydrogen or an optionally substituted alkyl group, alkenyl group, alkynyl group, alkadienyl group, haloalkyl group, aryl group, heteroaryl group, cycloalkyl group, bicycloalkyl group or heterocyclyl group Or R 1 and R 2 together with an adjacent nitrogen atom represent an optionally substituted heterocyclic ring,
    [43] R 3 represents a halogen atom or an alkyl group or an alkoxy group,
    [44] n represents an integer of 0 to 5,
    [45] Hal represents a halogen atom.
    [46] R 1 and R 2 together with the nitrogen atom in between represent a 4-methylpiperidine ring, in particular R 1 is a C 1-6 alkyl group (especially isopropyl group), C 1-6 haloalkyl group (especially , 2,2,2-trifluoroethyl or 1,1,1-trifluoroprop-2-yl group) or C 3-8 cycloalkyl group (in particular, cyclopentyl group or cyclohexyl group), and R 2 Is a hydrogen atom, n is 2 or 3, and R 3 groups are attached at 2-, 4- and 6-positions and represent a fluorine atom or a chlorine atom or a C 1-6 alkoxy group. .
    [47] In particular, the following azolopyrimidines are preferred: 5-chloro-6- (2-chloro-6-fluorophenyl) -7- (4-methylpiperid-1-yl)-[1,2,4] Triazolo [1,5-a] pyrimidine (azolopyrimidine A), 5-chloro-6- (2-chloro-6-fluorophenyl) -7- (2,2,2-trifluoroethyl Amino)-[1,2,4] triazolo [1,5-a] pyrimidine (azolopyrimidine B) and 5-chloro-6- (2,4,6-trifluorophenyl) -7- (1,1,1-trifluoroprop-2-ylamino)-[1,2,4] triazolo [1,5-a] pyrimidine (azolopyrimidine C).
    [48] Azolopyrimidine C is in the form of a racemic mixture or one enantiomer-rich (ee) compound because of the chirality of the 1,1,1-trifluoroprop-2-yl group, in particular (S) -azolopyrimidine C Can be applied as the abbreviated (S) -isomer.
    [49] Most preferred are mixtures of one or more compounds of Formula I and one or more fungicidal active ingredients that act as inhibitors of melanin biosynthesis, such as AC 382042.
    [50] As weeding agents, commercially available compounds selected from the group consisting of:
    [51] 2,4-D, 2,4-DB, 2,4-DP, acetochlor, asifluorophene, alachlor, alkoxydim, amethridion, amidosulfuron, asulam, atrazine, azisulsulfuron, ben Furesate, bensulfuron, bentazone, bifenox, bromobutide, bromoxynil, butachlor, carfenstrol, carfentrazone, chloridazone, chlorimuron, chlorprofam, chlorsulfuron, chlortol Luron, Cynmethylline, Cinosulfuron, Clomazone, Clopyralide, Cyanazine, Cycloate, Cyclosulfamuron, Cyclodimdim, Dimuron, Desmedipham, Di-Metazone, Dicamba, Diclobenyl , Diclofen, diflufenican, dimethenamid, dithiopyr, diuron, ephtam, esprocarb, ethiozin, phenoxaprop, flamprop-M-isopropyl, flamprop -M-methyl fluazifop, fluoromethuron, fluoroglycopene, flulidone, fluoxypyr, fluttamone, flutiamide, pomesafen, article Lufosinate, Glyphosate, Halosafen, Haloxypope, Hexazinone, Imazamabenz, Imazamaphyr, Imazamax, Imazafir, Imazaquin, Imazetapyr, Ioxynyl, Isoproturon , Isoxaben, isoxaplutol, lactofen, MCPA, MCPP, mefenacet, metabenzthiazuron, metamitrone, metazachlor, methyldimron, metolachlor, metribuzin, metsulfuron, molinate , Nicosulfuron, norflurazone, oryzaline, oxadiargyl, oxasulfuron, oxyfluorfen, pendimethalin, picloram. Pretilachlor, propachlor, propanyl, prosulfocarb, pyrazolsulfuron, pyridate, quinmerac, quinclolac, quizolopopetyl, cetoxydim, simethrin, sulfotion, sulfentrazone , Sulfosate, terbutryn, terbutylazine, thiamethuron, thifensulfuron, thiobencarb, tracoximide, trialate, triasulfuron, tribenuron, triclopyr, trituralin.
    [52] N- (4-fluorophenyl) 6- (3-trifluoromethylphenoxy) -pyrid, in particular also generally referred to as picolinafen, described, for example, in European patent application EP-A-0 447 004 Preference is given to derivatives of aryloxypicolinamides such as 2-ylcarboxamide.
    [53] Examples of insecticide compounds include alpha-cypermethrin, benfuracarb, BPMC, buprofezin, carbosulphan, cartaf, chlorfenbinfos, chlorpyriphos-methyl, cycloprotrin, cipermethrin, es Fenovalate, etofenprox, phenpropatrine, flucitrinate, flufenoxuron, hydrmethylnon, imidacloprid, isoxation, MEP, MPP, nitenpyram, PAP, fermethrin, propaphos , Pymetrozine, silafluorene, tebufenozide, teflubenzuron, temefos, terbufos, tetrachlorbinfos and triamate.
    [54] Generally non-aqueous SO preparations according to the invention comprise 15 to 400 g / L, preferably 20 to 200 g / L, in particular 25 to 100 g / L, of at least one crop protection active compound.
    [55] Preferably the vegetable oil ⒝ is selected from the group consisting of olive oil, soybean oil, orange oil and sunflower oil and is especially a mixture of triglycerides or triglycerides comprising the following fatty acids: palmitic acid, palmitoleic acid, stearic acid, oleic acid, linoleic acid, Linolenic acid.
    [56] Preference is given to vegetable oils having a density of less than 1 g / mL, preferably from 0.90 g / mL to 0.95 g / mL at 25 ° C.
    [57] Vegetable oils having the following characteristics * are most preferred.
    [58]
    [59] In general, the non-aqueous SO according to the present invention comprises 300 to 700 g / L, preferably 350 to 600 g / L, in particular 400 to 500 g / L, of at least one vegetable oil oil.
    [60] The polar aprotic solvent ⒞ used as cosolvent is necessary to increase the amount of active ingredient. Without this cosolvent, formulations made with less active ingredient dissolved in SO and an increased amount of solvent added to the plant may be phytotoxic. The polar solvent exhibits a dielectric constant of at least 2.5 at 25 ° C., in particular 2.7 to 4.0 at 25 ° C., with low solubility in water being preferred. Ketones such as cyclohexanone, lactones and amides such as γ-butyrolactone, in particular NC 1-18 alkylpyrrolidone , preferably NC 2-16 alkylpyrrolidone or NC 5-18 cycloalkylpyrrolidone Cyclic amides such as Most preferred are N-octylpyrrolidone and N-dodecylpyrrolidone. In another preferred embodiment of the invention the cosolvent is at least one, preferably two or three chemical formulas H 3 CO-CO- (CH 2 ) m -CO-OCH 3 , wherein m is 2, 3 or 4 Dimethyl dicarboxylate is included as a main component.
    [61] Particularly preferred is a mixture consisting of glutaric acid dimethyl ester, succinic acid dimethyl ester and adipic acid dimethyl ester, Lemro Chemieprodukte Michael Mrozyk KG, Grevenbroich, Germany Commercially available DBE is most preferred.
    [62] Generally nonaqueous SOs according to the invention comprise 30 to 200 g / L, preferably 50 to 150 g / L, in particular 75 to 125 g / L, of at least one polar aprotic solvent 톤.
    [63] According to the present invention, methylated vegetable oils used as nonpolar water immiscible cosolvents 는 are generally subjected to esterification reactions of medium-chain fatty acids with methanol or to transesterification reactions of those vegetable oils (preferably in the presence of lipases). Methyl ester obtainable by. The fatty acid of this vegetable oil is preferably 5 to 20 carbon atoms, especially 6 to 15 carbon atoms. In general, vegetable oils are mixtures of fatty acids having different chain lengths, with particular preference being given to mixtures of fatty acids having 10 carbon atoms as the main component which accounts for at least 50 percent of the mixture. In a preferred embodiment, the methylated vegetable oil used is a methyl ester of caprylic / capric acid or capric acid containing less than 5 percent of fatty acids of chain length other than 10 carbon atoms. In particular, methylated vegetable oils are marketed by Witconol 1095 and Witconol 2309 by Witco Corporation, Houston, Texas, USA, Houston, Texas, or by Henkel KGaA, Dusseldorf, Germany. Commercially available Edenor® ME C 6-10 and Edenor ME C 12 70 by KGaA, Duesseldorf, Germany are preferred. In general, the non-aqueous SO according to the invention comprises at least 100 g / L, preferably 150 to 450 g / L, in particular 250 to 400 g / L, of at least one methylated vegetable oil shock.
    [64] Suitable relative amounts of the active ingredient VII and vegetable oil VII according to the invention are from 1:50 to 1: 1, preferably from 1:30 to 1: 5, in particular from 1:20 to 1:10.
    [65] Recommended dosages for various uses of the plant protective active ingredient 되는 which enhance potency according to the present invention are known. Application of the SO formulation form proposed herein can reduce the amount of active ingredient per hectare required at that recommended amount (depending on the active ingredient, solvent and cosolvent and its amount), so that at an appropriate dosage It is possible to control more pests.
    [66] Important advantages in the use of the novel SO formulations are their rapid effect and high activity persistence. These benefits extend the spacing of pesticides and provide more flexibility.
    [67] Pesticide SO formulations according to the invention can be used for the protection and treatment of plants.
    [68] In a particularly preferred embodiment, the nonaqueous SO according to the invention
    [69] (B) 15 to 400 g / L, preferably 20 to 200 g / L, of at least one crop protecting active compound, in particular a compound of formula (I);
    [70] 300 300 to 700 g / L, preferably 350 to 600 g / L, of one or more vegetable oils selected from the group consisting of olive oil and sunflower oil;
    [71] (C) 30 to 200 g / L, preferably 50 to 150 g / L, of at least one polar aprotic solvent, in particular N-octylpyrrolidone or N-dodecylpyrrolidone;
    [72] (B) optionally comprising at least 450 g / L, preferably 200 to 400 g / L, methyl ester of at least one methylated vegetable oil, in particular caprylic and / or capric acid.
    [73] The solvents VII, VII and VII and the pesticide active ingredient VII are processed into the SO formulations according to the invention by well established processes. For example, a solvent may be added to make it meltable if necessary, and the solution may be dissolved in a suitable mixture of ⒝, ⒞ and ⒟.
    [74] SO formulations according to the invention are usually made of a stable liquid product and generally have from 1.5 to 40% w / v of active ingredient, from 30 to 70% w / v of vegetable oil, from 3 to 20% w / v of polar aproton Other additives such as an aqueous solvent, 0 to 45% w / v methylated vegetable oil, 0 to 10% w / v defoaming agent, corrosion inhibitor, stabilizer, penetrant and fixing agent and anionic and / or nonionic dispersants. .
    [75] The final non-aqueous SO formulation according to the invention is stable upon storage even if stored for a relatively long period of time, for example. SO according to the present invention can be contained in the formulation in one or more pesticide active ingredients in a high filling amount, providing the advantage as an optimal and manageable formulation of the crop protection active ingredient.
    [76] The solubility of the active ingredient VII in the formulations according to the invention depends not only on the structure of the active ingredient but also on the amount of cosolvent VII. When 10 to 15% of the cosolvent VII is included in the formulation, the relative amount of active ingredient VII increases by about 40 to 60%.
    [77] Preferably the SO formulations according to the invention are sprayed or sprinkled on the surface of the aquatic environment of discussion, in particular using a Shaker Bottle Application.
    [78] The formulation spreads well into monolayers on the water surface and sticks to the lipophilic surface of rice leaves.
    [79] Solid granules (eg granules as described in EP 10 415 569) in which the SO preparation according to the invention is adsorbed onto a solid carrier are also within the scope of the invention.
    [80] SO formulations comprising fungicides as the active ingredient VII described herein preferably have a fungicidal effect against one or more of the following diseases: leaf blight ( Xanthomonas campestris pv . Orizae , Xanthomonas campestris pv oryzae ), Blemishes ( Pyicularia oryzae ), Brown spots ( Cochliobolus miyabeanus ), Drake leg disease and Stem rot ( Gibberella Fujikuroi ), Leaf blight ( Rhizoctonia solani ) and hair blight ( Corticium rolfsii ). As used herein, the term "fungicidal effect" means that the active ingredient exhibits activity against diseases caused by the fungus.
    [81] For a clearer understanding of the invention, specific embodiments are described as follows. These examples are merely illustrative and are not to be understood in any way as limiting the principles underlying the scope of the invention. Various modifications of the invention in addition to those shown and described herein will become apparent to those skilled in the art from the following examples and the foregoing description. Such modifications are also intended to be included within the scope of the appended claims.
    [82] Examples of non-aqueous SO formulations according to the present invention are shown in Examples 1-4 below.
    [83] Compound Names of Components Used in the Examples
    [84]
    [85] <Example 1>
    [86] The following SO formulations according to the invention were prepared by dissolving the active ingredient in a mixture of solvents VII, VII and VII.
    [87] The following formulations were obtained:
    [88]
    [89] SO formulations exhibit the following properties:
    [90] Density = 0.921 g / mL; Flash point> 83 ° C .;
    [91] Upon storage at 0 ° C. for one week, no crystals formed.
    [92] <Example 2>
    [93] The following SO formulations according to the invention were prepared by dissolving the active ingredient in a mixture of solvents VII, VII and VII.
    [94] The following formulations were obtained:
    [95]
    [96] <Example 3>
    [97] The following SO formulations according to the invention were prepared by dissolving the active ingredient in a mixture of solvents VII, VII and VII.
    [98] The following formulations were obtained:
    [99]
    [100] <Example 4>
    [101] The following SO formulations according to the invention were prepared by dissolving the active ingredient in a mixture of solvents VII, VII and VII.
    [102] The following formulations were obtained:
    [103]
    [104] Control of Ficularia Orissa
    [105] Rice of the "Koshihikari" variety was cultivated in seedlings and planted in rice fields (four seedlings / holes) in a greenhouse 457 cm 2. Three days after transfer, several formulations of (S) -azolopyrimidine C were added to water. 45 days after treatment with the active ingredient, the spore solution in Pyricularia Orissa was inoculated. Untreated rice was included in this test.
    [106] A. Rice Leaf Fever
    [107] At 53 days after treatment, 63% of the untreated rice (control) leaf area was infected with rice blasts. The incidence level of treated rice (% of infected leaf area) was also assessed and the efficacy of the treatment (%) was also measured. The effects of the SO formulations and granule formulations according to the invention are in Table I.
    [108]
    [109] B. Rice Ear Blast
    [110] At 126 days after treatment, 60% of untreated rice ears (control) were infected with rice blasts. The incidence level of the treated plants (% of infected rice ear) was also assessed and the efficacy of the treatment (%) was also measured. The effects of the SO formulations and granule formulations according to the invention are in Table II.
    [111]
    [112] Compared with conventional granule formulations, this test clearly demonstrates that a dose reduction of about 50% can be achieved with equivalent disease control when treated with the SO formulations according to the invention.
    [113] In addition, phytotoxicity was negligible at the tested dose.
    [114] In addition, the SO formulations of the present invention are much more environmentally friendly than conventional formulations and have improved toxicological characteristics, making the formulations safer to operate.
    权利要求:
    Claims (12)
    [1" claim-type="Currently amended] 15 15 to 400 g / L of one or more crop protection active compounds;
    300 300 to 700 g / L of one or more vegetable oils;
    30 30 to 200 g / L of one or more polar aprotic organic solvents;
    ⒟ optionally at least one methylated vegetable oil
    A non-aqueous stable concentrated single phase sleeping oil (SO) formulation of a crop protection active compound, comprising a total of 1 liter of all components in the formulation.
    [2" claim-type="Currently amended] The SO formulation of claim 1, comprising 100 to 450 g / L of one or more methylated vegetable oils.
    [3" claim-type="Currently amended] The SO preparation according to claim 1, wherein the crop protection active compound V contains at least one triazolopyrimidine of the general formula (I).
    <Formula I>

    Wherein R 1 and R 2 are each independently hydrogen or an optionally substituted alkyl group, alkenyl group, alkynyl group, alkadienyl group, haloalkyl group, aryl group, heteroaryl group, cycloalkyl group, bicycloalkyl group or heterocyclyl group Or R 1 and R 2 together with an adjacent nitrogen atom represent an optionally substituted heterocyclic ring,
    R 3 represents a halogen atom, an alkyl group or an alkoxy group,
    n represents an integer of 0 to 5,
    Hal represents a halogen atom.
    [4" claim-type="Currently amended] The SO preparation according to claim 1, wherein the vegetable oil soap is selected from the group consisting of olive oil, soybean oil, orange oil and sunflower oil.
    [5" claim-type="Currently amended] 2. The SO preparation according to claim 1, wherein said vegetable oil weng is a triglyceride or a mixture of triglycerides composed mainly of fatty acids of palmitic acid, palmitoleic acid, stearic acid, oleic acid, linoleic acid, linolenic acid.
    [6" claim-type="Currently amended] The SO preparation according to claim 1, wherein the ratio of the crop protection active compound ⒜ to the vegetable oil ⒝ is 1:50 to 1: 1, preferably 1:30 to 1: 5.
    [7" claim-type="Currently amended] According to claim 1, wherein one polar aprotic organic solvent ⒞ the NC 1-14 alkyl-pyrrolidone, NC 5- 8 cycloalkyl-pyrrolidone, selected from the group consisting of a lactone and cyclohexanone as γ- butyronitrile SO formulation.
    [8" claim-type="Currently amended] 8. The SO formulation of claim 7, wherein the polar aprotic organic solvent VII is N-octylpyrrolidone or N-dodecylpyrrolidone.
    [9" claim-type="Currently amended] The SO formulation of claim 2, wherein the methylated vegetable oil VII is a C 10 -methylated fatty acid.
    [10" claim-type="Currently amended] The SO preparation according to claim 2, wherein the methylated vegetable oil is methyl ester obtained from palm kernel oil.
    [11" claim-type="Currently amended] A method of controlling plant diseases and / or pests in an aquatic environment, comprising treating the SO formulation of claim 1 with water so that the oily membrane spreads over the water and the active ingredient contained in the SO formulation is in contact with the plant.
    [12" claim-type="Currently amended] In aquatic environments of rice
    (Iii) at least one vegetable oil,
    (Ii) at least one polar aprotic organic solvent; And
    (Iii) optionally at least one methylated vegetable oil
    A method of enhancing the efficacy of a compound of formula (I) comprising applying an effective amount of at least one compound of formula (I) dissolved in a mixture comprising as a main component.
    <Formula I>

    Wherein R 1 , R 2 , R 3 , Hal and n are the meanings as defined in claim 2.
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    同族专利:
    公开号 | 公开日
    BR0015677A|2002-08-06|
    CO5221072A1|2002-11-28|
    KR100766638B1|2007-10-15|
    MY128413A|2007-01-31|
    JP2003513989A|2003-04-15|
    TWI236872B|2005-08-01|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1999-11-18|Priority to US44282299A
    1999-11-18|Priority to US09/442,822
    2000-11-16|Application filed by 스타르크, 카르크, 바스프 악티엔게젤샤프트
    2002-07-13|Publication of KR20020059748A
    2007-10-15|Application granted
    2007-10-15|Publication of KR100766638B1
    优先权:
    申请号 | 申请日 | 专利标题
    US44282299A| true| 1999-11-18|1999-11-18|
    US09/442,822|1999-11-18|
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