• 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:
    METHOD FOR PREPARING MEANS FOR THE FIGHT AGAINST ECOLOGICAL PARAMETERS OF ANIMALS on the basis of the active compound - complex pentafluoroben. 2,2-dimethyl-3- methyl ether
    公开号:SU1077554A3
    申请号:SU813296478
    申请日:1981-06-08
    公开日:1984-02-29
    发明作者:Дорн Губерт；Штендель Вильгельм；Феге Герберт
    申请人:Байер Аг (Фирма)；
    IPC主号:
    专利说明:

    1 vi
    U1
    : jfi
    4 The invention relates to veterinary medicine, in particular to a method for preparing and a means for combating ectoparasites of animals. A known method of preparing an agent for controlling ectoparasites of animals on the basis of active hydrodehyde, 2,2-dimethyl-3 (2,2-dichloroinvm) -cyclopropanecarboxylic acid complex pentafluorobenzyl ester or 2 isopropoxyphenyl-N-methylcarbamate, dissolves it in an organic a solvent of ethanol or isopropanol and mixing with the suspension stabilizer, which is colloid silicic acid or its mixture with yellow iron oxide pigment fl. The disadvantage of this method is that emogo usual means but which is applied to the skin of animals, is its poor iztza insufficient action of the residual. The purpose of the invention is to increase the ac. means by increasing its residual effect. This goal is achieved by introducing into the solution of the active compound with a solvent a water-soluble polymer that forms a gel — sodium alginate or propylene glycol sodium alginate from a calculation, 10 parts by weight. per 100 weight hours means when the content of the active compound in the solution is 0.1-15%,. ia after the introduction of the water-soluble polymer, stabilization is added to the mixture. -izator in the amount of 2-7% by weight of the suspension. Ingredients I-V1I and AZ are as follows: 1ft Pentafluoro-benzyl O-ester 2,2-dimethyl 3- (2,2-dichlorovinyl) -cyclopropane carboxylic acid, g Propylene glycol alginate, g, 10.0 Colloidal silicic acid, g 5 , 0 Yellow pigment of iron oxide, g. 2.0 2.0 To 100 Isopropanol, g To 100.0 ml ml 2.2-limethyl-3- (2, 2-dichlorovinyl) -cyclopropanecarboxylic acid, complex pentafluorononyl ester, g 0.1 Sodium alginate, g 10.0 Colloidal silicic acid, g 5.0 5.0 Yellow pigment 3.0 3.0 3.0. iron b, g Isopropdol To Up to 100 100.0 ml 2.2-dimethyl-3- (2.2 dichloro and silt) pentafluorobenzyl ester, g Sodium alginate, g 10.0 Colloidal silicic acid, g 2.0 2.0 To 100.0 Pre-ethanol ml 100 ml of 2,2-dimethyl-3- (2,2-Dichlorvil) -cycloprene lancarboxylic acid pentafluorobenzyl ester. Sodium alginate, g Colloidal cream 2, 0 2,0 nievy acid, g To Do Ethanol 100,0 100 M / I MP 2-Nzopropoxyphenyl 15, d 15,0 -N-methylcarbamate, g 10,0 Sodium alginate, g Colloidal creme 2 , 0 2.0 nievy acid, g To Isopropaiol 100.0 “So. MP 2-Isopropoxyphenyl5.0.0.0-n-methylcarbamate, g 10.0 Sodium alginate, g Colloidal cream2, 0 2.0 nieva acid, g To Do Ethanol 100.0 100 ml ml
    权利要求:
    Claims (1)
    [1]
    METHOD FOR PREPARING AN AGENT ECTOPARASITES AGENT Based on the active compound - 2,2-dimethyl-3- (2,2-dichlorovinyl) -cyclopropanecarboxylic acid pentafluorobenzyl ester or 2-is0Nropoxyphenyl-k-me. tilcarbamate, including dissolving it in an organic solvent, ethanol or isopropanol; crosslinking with a suspension stabilizer. Il ... which is colloidal silicic acid or its mixture with a yellow pigment of iron oxide, characterized in that, in order to increase the activity of the agent by increasing its residual effect, a water-soluble polymer is introduced into the solution of the active compound with a solvent, forming gel - sodium alginate or prfpilenglikol sodium alginate from the calculation of 10 parts by weight per 100 parts by weight means when the content of the active compound in the solution is 0.1-15%, and after the introduction of a water-soluble polymer to the mixture is added. stabilizer in the amount of 2-7% RT weight suspensions.
    m SU <„4077554 A
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    同族专利:
    公开号 | 公开日
    DE3021725A1|1981-12-17|
    DK251081A|1981-12-11|
    DK155141B|1989-02-20|
    EP0041654A1|1981-12-16|
    EP0041654B1|1983-09-21|
    PL231562A1|1982-01-18|
    AR226359A1|1982-06-30|
    US4568541A|1986-02-04|
    AU538164B2|1984-08-02|
    JPS5726601A|1982-02-12|
    DK155141C|1989-07-17|
    IL63048D0|1981-09-13|
    AU7142781A|1981-12-17|
    ES8705192A1|1987-05-01|
    NZ197332A|1984-02-03|
    JPH0148241B2|1989-10-18|
    PH16426A|1983-10-03|
    BR8103636A|1982-03-02|
    DE3160946D1|1983-10-27|
    ZA813849B|1982-06-30|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US3399991A|1964-05-05|1968-09-03|Du Pont|Freeze-resistant pesticidal composition|
    US3301808A|1964-05-12|1967-01-31|Gen Aniline & Film Corp|Aqueous aerosol film forming compositions|
    DE1617282A1|1965-11-30|1975-02-06|Astra Pharma Prod|DEVICE FOR LOCAL ANESTHETIZATION BY LOCAL APPLICATION AND METHOD FOR MANUFACTURING THIS DEVICE|
    US3590118A|1969-11-03|1971-06-29|Goodrich Co B F|Long lasting insect repellent films for skin and other substrates|
    GB1394990A|1971-08-12|1975-05-21|Hydrophilics Int Inc|Copolymers and compositions containing copolymers|
    FR2216921A1|1973-02-09|1974-09-06|Pepro|
    GB1451473A|1973-05-18|1976-10-06|Beecham Group Ltd|Insecticidal gels|
    US4178361A|1973-09-10|1979-12-11|Union Corporation|Sustained release pharmaceutical composition|
    DE2541087A1|1974-09-19|1976-04-15|Hydrophilics Int Inc|MEANS AND METHODS USED IN AGRICULTURE|
    US4183950A|1976-12-22|1980-01-15|Bayer Aktiengesellschaft|Combating arthropods with 2,2-dimethyl-3-vinyl-cyclopropane carboxylic acid esters of halogenated benzyl alcohols|
    DE2658725A1|1976-12-24|1978-07-06|Bayer Ag|AGENT FOR CONTROLLING ANIMAL EECTOPARASITES WITH A STRONG RESIDUAL EFFECT|DE3041814A1|1980-11-06|1982-06-03|Bayer Ag, 5090 Leverkusen|FORMULA FOR CONTROLLING ANIMAL EECTOPARASITES, IN PARTICULAR INSECTS AND ACARINES|
    US4938951A|1980-12-30|1990-07-03|Union Carbide Chemicals And Plastics Company Inc.|Potentiation of topical compositions wherein a uniform microdispersion of active agent is formed|
    JPS57123112A|1980-12-30|1982-07-31|Union Carbide Corp|Effect increase of local composition|
    NO151026C|1982-11-26|1985-01-30|Saetersmoen A S|INSECTICID AND AKARICID MIXTURE CONTAINING GELATIN, AND USING THE MIXTURE FOR AA FIGHTING INSECT AND MEDICINE|
    CA1256366A|1983-10-21|1989-06-27|George B. Marks, Sr.|In situ insecticide|
    US4762718A|1984-07-20|1988-08-09|Fearing Manufacturing Co., Inc.|In situ insecticide|
    US4783335A|1985-11-18|1988-11-08|The Kendall Company|Controlled topical application of bioactive reagent|
    GB8612826D0|1986-05-27|1986-07-02|Boots Co Plc|Insecticidal compositions|
    FR2599220A1|1986-05-29|1987-12-04|Aerosols Ste Mediterraneenne|New parasiticidal composition having prolonged effect for prevention or external treatment in man and warm-blooded animals|
    GB8902929D0|1989-02-09|1989-03-30|Ici Plc|Insecticide treatment & compositions therefor|
    US5221698A|1991-06-27|1993-06-22|The Regents Of The University Of Michigan|Bioactive composition|
    GB9318869D0|1993-09-11|1993-10-27|Pisacane Anthony|Repellant material|
    DE4417742A1|1994-05-20|1995-11-23|Bayer Ag|Non-systemic control of parasites|
    US8110608B2|2008-06-05|2012-02-07|Ecolab Usa Inc.|Solid form sodium lauryl sulfatepesticide composition|
    US8968757B2|2010-10-12|2015-03-03|Ecolab Usa Inc.|Highly wettable, water dispersible, granules including two pesticides|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    DE19803021725|DE3021725A1|1980-06-10|1980-06-10|AGENT FOR CONTROLLING ANIMAL EECTOPARASITES WITH A STRONG RESIDUAL EFFECT|
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