• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    A pesticidal composition comprising (A) 2-CHLORO-1-(2,4-DICHLOROPHENYL)VINYL DIETHYL PHOSPHATE, COMMONLY CALLED CHLOROFENVINPHOS, AND (B) AT LEAST ONE PYRETHROID COMPOUND.
    公开号:SU735150A3
    申请号:SU782565050
    申请日:1978-01-13
    公开日:1980-05-15
    发明作者:Клиффорд Фелтон Джон；Стеварт Бадмин Джон
    申请人:Шелл Интернэшнл Рисерч Маатсхаппий Б.В. (Фирма)；
    IPC主号:
    专利说明:

    . . . . one .
    This invention relates to a chemical plant protection agent, namely, an insecticoacaricidal composition. Based on 2-HLOR-1- (2,4-dichlorophenyl) -vinyl diethyl phosphate, .5
    It is already known that derivatives of cycloceropanecarboxylic acids are used as insecticides {),
    It is also known that 2-chloro-1- (2-4-dichlorophenyl) vinyl diethyl phosphate (chlor-30. Pheninphos) is used as an insecticide 2.. ...
    However, these compounds are not sufficiently active.
    The aim of the invention is to create an insecticoacaricidal composition having a high insecticacaricidal activity or an active substance basis that, when used together, exhibits a synergistic effect ...
    This goal is achieved using an insecticoacaricidal composition containing 2-chloro-1- (2,4-dichlorophenyl) -vinyl diethyl phosphate as an active substance with the addition of a phenoxybenzyl ester derivative of the general formula
    About B I A- 3-0-sa H / -v-l / 30
    2
    where R is hydrogen, cyan,
    A - 2- (2,2-dichlorovinyl) -3,3-dimethylcyclopropyl, c-isopropyl-4-chlorobenzyl.
    The weight ratio of components in the composition of 5: 1 - 25: 1.
    The content of the active substance in the composition is 1-50 wt.%, The rest is additive.
    The form of application of the composition is conventional: dispersions, emulsions, powders. They are prepared by methods that are common in the manufacture of first items. forms of pesticides.
    The following are formulas of the compounds tested in the examples.
    Compound A
    n dtt-ecig
    Nightclub
    Compound B
    H
    BUT
    n, s
    JooSng
    N N
    x /
    Shch
    Two- and three-day-old flies are anaesthetized with carbon dioxide and 1 μl of the test solution Veod t with a micrometric syringe into the bruine portion of each flour, with 20 flies being tested. The treated flies are in glass cans covered with a thin cloth, held on elastic ties. Cotton swabs are soaked with sugar solution and placed on top of the fabric as food. After 24 h, the death rate of the flies was maximum in each experiment. From these results, the sotoxicity coefficient is calculated in micrograms of active material. These results are presented in Table. one.
    Table 1
    CompoundA Chlorfenvinfos Compound A chlorfenvinfos
    Example 2. The activity of the mixture against tick cattle
    The coefficient of the toxicity of mixtures of compounds A, B and B with chlorfenvinphos is determined by the Johnson-Soun method.
    The cattle mite used in this example is resistant to the Bufilus strain. Mycroplus Because of the difficulty we define, the mites are alive or not, the activity of the compounds and their mixtures are expressed as a precursor for the reduction of deposited eggs.
    The compound and their mixtures test 1Gt1 of Zychyskye yateryyy jjaffvb nnye in acetone ..
    Female tick killing is done in petri dishes. 2 ml test p
    Compound A: Chlorfenvinfos
    Compound B Chlorfenvinfos
    Medium B: Chlorfenvinfos
    Compound C Chlorfenvinfos
    Compound B: Chlorfenvinfos
    0,0029 0,066
    0,017
    131
    solution take a micrometric syringe. cement and injected into the abdominal cavity of each .. "tick." Ticks are treated with solutions of a certain concentration.
    The treated ticks were incubated for 14 days in an incubator at 30% humidity. Then, the number of eggs deposited during this period is determined, and thereafter, the percentage of hatching.
     Compounds and mixtures thereof are determined by the Percentage of reducing the number of deposited eggs. From the obtained results, the activity of LDE compounds of microorganisms and the coefficient of sotoxicity are determined. Results are shown in Table. 2
    Table 2
    278
    222
    262
    Thus, the proposed compositions have high activity and exhibit a synergistic effect.
    权利要求:
    Claims (1)
    [1]
    Invention Formula
    An insecticoacaricidal composition containing 2-chloro-1- (2,4-dichlorophenyl) vinyl diethylphosphate as an active substance and an additive selected from the group that includes a solid carrier, a liquid carrier, and a surface active agent that, in order to enhance insect-acaricidal activity and the manifestation of a synergistic effect, it additionally contains a derivative of phenoxybenzyl ether of the general formula
    类似技术:
    公开号 | 公开日 | 专利标题
    US4889872A|1989-12-26|2,3,5,6-Tetrafluorobenzyl | 1r-trans-2,2-dimethyl-3-|-cyclopropanecarboxylate
    CN102113510B|2013-03-20|Insecticidal composition containing metaflumizone
    SU735150A3|1980-05-15|Insecticide-acaricide
    US4904645A|1990-02-27|Environmentally safe, broad spectrum insecticide
    EP0018406A1|1980-11-12|Insect control methods using abscisic acid
    IL24008A|1969-01-29|Insecticidal compositions comprising an insecticide and a synergistic methylenedioxyphenyl-compound
    DE1097750B|1961-01-19|Insect repellants
    JP3115137B2|2000-12-04|Insecticidal efficacy enhancer and liquid insecticide preparation containing the same
    EP0266822A1|1988-05-11|Use of farnesene in agriculture or horticulture or in the protection of stocks, or for the preparation of products, and also method for controlling insects and acarids by using farnesene
    US3535424A|1970-10-20|Insecticidal 1 - | - 2-mono or disubstituted ethylenes
    US4239774A|1980-12-16|Pesticidal compositions containng 1,3,5-triazapenta-1,4-diene and organo-tin oxide compounds
    US4000266A|1976-12-28|Synergistic combination of insecticides
    US3179557A|1965-04-20|N-methyl-phenyl carbamates for controlling animal pests
    EP0091616B1|1985-09-25|Acaricide compositions
    CH616313A5|1980-03-31|Process for the preparation of novel phenoxybenzyl esters of spirocarboxylic acids and their optical and geometric isomers
    US4517201A|1985-05-14|Synergistic compositions and methods of combating insects employing amitraz and cypermethrin
    US3010871A|1961-11-28|Method of destroying mites employing the p-bromophenyl ester of benzenesulfonic acid
    US4657936A|1987-04-14|Halogenated saturated hydrocarbons as acaricidal compounds
    US3830887A|1974-08-20|O,o-diloweralkyl-o-|thiophosphates
    US4166130A|1979-08-28|Pesticidal compositions
    JP2729397B2|1998-03-18|Acaricide composition
    US4216213A|1980-08-05|Acaricidal and insecticidal compositions
    US3644633A|1972-02-22|Method for combating soil insects and termites
    US3256145A|1966-06-14|Synergistic pesticidal composition
    IE45143B1|1982-06-30|Improvements in or relating to pesticides
    同族专利:
    公开号 | 公开日
    NL7801326A|1978-08-10|
    FR2379252A1|1978-09-01|
    IT1093643B|1985-07-19|
    PL204472A1|1978-11-06|
    SE7801368L|1978-08-09|
    IE780256L|1978-08-08|
    DK157424B|1990-01-08|
    DE2804946C2|1989-08-31|
    LU79019A1|1978-09-28|
    IT7820038D0|1978-02-06|
    AU3302078A|1979-08-16|
    AU522010B2|1982-05-13|
    GB1595081A|1981-08-05|
    TR19930A|1980-04-30|
    CA1111760A|1981-11-03|
    BR7800685A|1978-10-31|
    US4144331A|1979-03-13|
    CS194834B2|1979-12-31|
    HU184676B|1984-09-28|
    NZ186407A|1980-08-26|
    AR225479A1|1982-03-31|
    IE46400B1|1983-06-01|
    DD134036A5|1979-02-07|
    AR228830A1|1983-04-29|
    ZA78712B|1979-01-31|
    DE2804946A1|1978-08-10|
    DK52878A|1978-08-09|
    PL107728B1|1980-02-29|
    BE863663A|1978-08-07|
    GR64494B|1980-03-31|
    FR2379252B1|1980-04-04|
    JPS5399326A|1978-08-30|
    SE430846B|1983-12-19|
    DK157424C|1990-06-05|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    CA693024A|1958-06-10|1964-08-25|Allied Chemical Corporation|Vinyl phosphate insecticides|
    US2956073A|1960-04-13|1960-10-11|Shell Oil Co|Insecticidally active esters of phosphorus acids and preparation of the same|
    NL290307A|1962-03-19|
    US3991213A|1968-06-08|1976-11-09|Showa Denko Kabushiki Kaisha|Pesticidal composition|
    BE794926A|1971-04-23|1973-08-02|Shell Int Research|BIOLOGICALLY ACTIVE COMPOSITIONS|
    JPS515450B1|1971-06-29|1976-02-20|
    US4024163A|1972-05-25|1977-05-17|National Research Development Corporation|Insecticides|
    EG11383A|1972-07-11|1979-03-31|Sumitomo Chemical Co|Novel composition for controlling nixious insects and process for preparing thereof|
    JPS49132241A|1973-04-24|1974-12-18|
    GB1437815A|1973-05-15|1976-06-03|
    JPS5058237A|1973-09-28|1975-05-21|
    US3987193A|1974-12-03|1976-10-19|Shell Oil Company|Pesticidal dihalovinyl-spiroalkanecyclopropane derivatives|
    DE2706222A1|1976-02-16|1977-08-18|Ciba Geigy Ag|CYCLOPROPANCARBONIC ACID ESTERS, METHOD OF MANUFACTURING AND USING them|
    NZ186081A|1976-12-24|1982-03-09|Wellcome Found|Ectoparasiticidal compositions containing a pyrethroid and an organophosphorus compound|
    GB1592056A|1976-12-24|1981-07-01|Wellcome Found|Synergistic parasiticidal compositions|AU531541B2|1979-05-11|1983-08-25|Pitman-Moore Australia Limited|Tickicidal composition|
    DE2922481A1|1979-06-01|1980-12-11|Bayer Ag|ELECTROPARASITICIDES CONTAINING SUBSTITUTED PHENOXYBENZYLOXYCARBONYL DERIVATIVES,PHOSPHORIC ACID ESTERS, PROCESS FOR THEIR PRODUCTION AND THEIR USE AS EECTOPARASICIDES|
    ZA805747B|1979-09-19|1981-09-30|Shell Res Ltd|Pesticidal compositions|
    US4301155A|1979-10-01|1981-11-17|The Dow Chemical Company|Insecticidal synergistic mixtures of O,O-diethyl O-phosphorothioate and 2,2,3,3-tetramethylcyclopropanecarboxylic acid:cyanomethyl ester|
    US4301154A|1979-10-01|1981-11-17|The Dow Chemical Company|Insecticidal synergistic mixtures of 0,0-diethyl 0-phosphorothioate and 3--2,2-dimethylcyclopropane carboxylic acid:cyanomethyl ester|
    US4301156A|1979-10-01|1981-11-17|The Dow Chemical Company|Insecticidal synergistic mixtures of O,O-diethyl O- phosphorothioate and 4-chloro-α-benzeneacetic acid:cyano methyl ester|
    US4263287A|1979-11-02|1981-04-21|Stauffer Chemical Company|Fenvalerate-phosmet insecticidal composition|
    ZA806984B|1979-11-14|1981-11-25|Shell Res Ltd|Pesticidal compositions|
    DE4417742A1|1994-05-20|1995-11-23|Bayer Ag|Non-systemic control of parasites|
    EP3013196B1|2013-06-26|2019-03-06|Nestec S.A.|Volumetric heating device for beverage or food preparation machine|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    GB5112/77A|GB1595081A|1977-02-08|1977-02-08|Pesticidal composition|
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