CA1142851A - Compositions tiquicides synergiques - Google Patents

Compositions tiquicides synergiques

Info

Publication number: CA1142851A
Authority: CA; Canada
Prior art keywords: chloro; diethyl; phosphorothioate; composition; component
Prior art date: 1980-05-21
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA000352319A

Other languages

English (en)

Inventor

Vincent K. Stubbs

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Orica Ltd

Original Assignee

ICI Australia Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1980-05-21

Filing date

1980-05-21

Publication date

1983-03-15

1980-05-21 Application filed by ICI Australia Ltd filed Critical ICI Australia Ltd

1980-05-21 Priority to CA000352319A priority Critical patent/CA1142851A/fr

1983-03-15 Application granted granted Critical

1983-03-15 Publication of CA1142851A publication Critical patent/CA1142851A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 63
230000002195 synergetic effect Effects 0.000 title abstract 2
241000238680 Rhipicephalus microplus Species 0.000 claims abstract description 20
238000000034 method Methods 0.000 claims abstract description 20
-1 cyclopropanecarboxylic acid ester Chemical class 0.000 claims abstract description 12
150000002903 organophosphorus compounds Chemical class 0.000 claims abstract description 11
239000004480 active ingredient Substances 0.000 claims description 20
239000001257 hydrogen Substances 0.000 claims description 8
229910052739 hydrogen Inorganic materials 0.000 claims description 8
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 7
239000000460 chlorine Substances 0.000 claims description 7
229910052801 chlorine Inorganic materials 0.000 claims description 6
RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 claims description 6
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 5
150000007942 carboxylates Chemical class 0.000 claims description 5
239000011737 fluorine Substances 0.000 claims description 5
229910052731 fluorine Inorganic materials 0.000 claims description 5
150000002431 hydrogen Chemical class 0.000 claims description 5
NAGJZTKCGNOGPW-UHFFFAOYSA-K dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [O-]P([O-])([S-])=S NAGJZTKCGNOGPW-UHFFFAOYSA-K 0.000 claims description 4
229910052717 sulfur Inorganic materials 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
PKUWKAXTAVNIJR-UHFFFAOYSA-N O,O-diethyl hydrogen thiophosphate Chemical compound CCOP(O)(=S)OCC PKUWKAXTAVNIJR-UHFFFAOYSA-N 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 claims 2
CZGGKXNYNPJFAX-UHFFFAOYSA-N Dimethyldithiophosphate Chemical compound COP(S)(=S)OC CZGGKXNYNPJFAX-UHFFFAOYSA-N 0.000 claims 1
PCXMHWMAMMBLFG-UHFFFAOYSA-N [2-chloro-2-(2,4-dichlorophenyl)ethenyl] diethyl phosphate Chemical compound CCOP(=O)(OCC)OC=C(Cl)C1=CC=C(Cl)C=C1Cl PCXMHWMAMMBLFG-UHFFFAOYSA-N 0.000 claims 1
230000000749 insecticidal effect Effects 0.000 claims 1
241000238876 Acari Species 0.000 abstract description 17
206010061217 Infestation Diseases 0.000 abstract description 5
230000008029 eradication Effects 0.000 abstract description 5
230000002265 prevention Effects 0.000 abstract description 3
241000283690 Bos taurus Species 0.000 description 15
150000001875 compounds Chemical class 0.000 description 15
239000000306 component Substances 0.000 description 13
RIZMRRKBZQXFOY-UHFFFAOYSA-N ethion Chemical compound CCOP(=S)(OCC)SCSP(=S)(OCC)OCC RIZMRRKBZQXFOY-UHFFFAOYSA-N 0.000 description 12
KWGUFOITWDSNQY-UHFFFAOYSA-N Bromophos-ethyl Chemical group CCOP(=S)(OCC)OC1=CC(Cl)=C(Br)C=C1Cl KWGUFOITWDSNQY-UHFFFAOYSA-N 0.000 description 9
241001465754 Metazoa Species 0.000 description 7
SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 7
229910052760 oxygen Inorganic materials 0.000 description 7
241001481703 Rhipicephalus <genus> Species 0.000 description 6
239000007787 solid Substances 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
239000000463 material Substances 0.000 description 5
239000000843 powder Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
FSAVDKDHPDSCTO-WQLSENKSSA-N [(z)-2-chloro-1-(2,4-dichlorophenyl)ethenyl] diethyl phosphate Chemical compound CCOP(=O)(OCC)O\C(=C/Cl)C1=CC=C(Cl)C=C1Cl FSAVDKDHPDSCTO-WQLSENKSSA-N 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
BXNANOICGRISHX-UHFFFAOYSA-N coumaphos Chemical compound CC1=C(Cl)C(=O)OC2=CC(OP(=S)(OCC)OCC)=CC=C21 BXNANOICGRISHX-UHFFFAOYSA-N 0.000 description 4
YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical class OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 description 4
FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 4
JISACBWYRJHSMG-UHFFFAOYSA-N famphur Chemical compound COP(=S)(OC)OC1=CC=C(S(=O)(=O)N(C)C)C=C1 JISACBWYRJHSMG-UHFFFAOYSA-N 0.000 description 4
238000009472 formulation Methods 0.000 description 4
PNVJTZOFSHSLTO-UHFFFAOYSA-N Fenthion Chemical compound COP(=S)(OC)OC1=CC=C(SC)C(C)=C1 PNVJTZOFSHSLTO-UHFFFAOYSA-N 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
241000607479 Yersinia pestis Species 0.000 description 3
150000001409 amidines Chemical class 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
YMGUBTXCNDTFJI-UHFFFAOYSA-M cyclopropanecarboxylate Chemical compound [O-]C(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-M 0.000 description 3
238000010410 dusting Methods 0.000 description 3
125000000623 heterocyclic group Chemical group 0.000 description 3
239000007788 liquid Substances 0.000 description 3
229910052698 phosphorus Inorganic materials 0.000 description 3
239000011574 phosphorus Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000008247 solid mixture Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000007921 spray Substances 0.000 description 3
238000003860 storage Methods 0.000 description 3
QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
VEDTXTNSFWUXGQ-UHFFFAOYSA-N Carbophenothion Chemical compound CCOP(=S)(OCC)SCSC1=CC=C(Cl)C=C1 VEDTXTNSFWUXGQ-UHFFFAOYSA-N 0.000 description 2
LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 description 2
VBKKVDGJXVOLNE-UHFFFAOYSA-N Dioxation Chemical compound CCOP(=S)(OCC)SC1OCCOC1SP(=S)(OCC)OCC VBKKVDGJXVOLNE-UHFFFAOYSA-N 0.000 description 2
241000238889 Ixodidae Species 0.000 description 2
CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
241000403354 Microplus Species 0.000 description 2
239000000654 additive Substances 0.000 description 2
229910052785 arsenic Inorganic materials 0.000 description 2
RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
125000001309 chloro group Chemical group Cl* 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
229950011148 cyclopropane Drugs 0.000 description 2
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
125000004188 dichlorophenyl group Chemical group 0.000 description 2
WGWJBWHBOKETRC-UHFFFAOYSA-N diethoxy-(3-methyl-4-methylsulfanylphenoxy)-sulfanylidene-$l^{5}-phosphane Chemical group CCOP(=S)(OCC)OC1=CC=C(SC)C(C)=C1 WGWJBWHBOKETRC-UHFFFAOYSA-N 0.000 description 2
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
235000019000 fluorine Nutrition 0.000 description 2
229940060037 fluorine Drugs 0.000 description 2
125000001153 fluoro group Chemical group F* 0.000 description 2
239000008187 granular material Substances 0.000 description 2
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
239000012669 liquid formulation Substances 0.000 description 2
230000007774 longterm Effects 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
239000002736 nonionic surfactant Substances 0.000 description 2
239000000375 suspending agent Substances 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
IKFQCPLFVFOGMV-UHFFFAOYSA-N (2-chloro-3,3,3-trifluoroprop-1-enyl) 2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)CC1C(=O)OC=C(Cl)C(F)(F)F IKFQCPLFVFOGMV-UHFFFAOYSA-N 0.000 description 1
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
208000031295 Animal disease Diseases 0.000 description 1
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
241000282472 Canis lupus familiaris Species 0.000 description 1
241001480824 Dermacentor Species 0.000 description 1
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
241000283086 Equidae Species 0.000 description 1
241000238631 Hexapoda Species 0.000 description 1
241001480803 Hyalomma Species 0.000 description 1
241000238681 Ixodes Species 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
241001494479 Pecora Species 0.000 description 1
239000005921 Phosmet Substances 0.000 description 1
TZBPRYIIJAJUOY-UHFFFAOYSA-N Pirimiphos-ethyl Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(N(CC)CC)=N1 TZBPRYIIJAJUOY-UHFFFAOYSA-N 0.000 description 1
208000005374 Poisoning Diseases 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
239000005864 Sulphur Substances 0.000 description 1
241000251539 Vertebrata <Metazoa> Species 0.000 description 1
239000002253 acid Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000007824 aliphatic compounds Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
JYZIHLWOWKMNNX-UHFFFAOYSA-N benzimidazole Chemical compound C1=C[CH]C2=NC=NC2=C1 JYZIHLWOWKMNNX-UHFFFAOYSA-N 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical group [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000002775 capsule Substances 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 1
229960005286 carbaryl Drugs 0.000 description 1
239000000969 carrier Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
230000000332 continued effect Effects 0.000 description 1
230000002079 cooperative effect Effects 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
OMYMWKVYKBYCBS-UHFFFAOYSA-N diethoxy-(6-methyl-2-propan-2-ylpyrimidin-4-yl)oxy-sulfanylidene-$l^{5}-phosphane;trihydroxy(sulfanylidene)-$l^{5}-phosphane Chemical compound OP(O)(O)=S.CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 OMYMWKVYKBYCBS-UHFFFAOYSA-N 0.000 description 1
UCQFCFPECQILOL-UHFFFAOYSA-N diethyl hydrogen phosphate Chemical compound CCOP(O)(=O)OCC UCQFCFPECQILOL-UHFFFAOYSA-N 0.000 description 1
238000007865 diluting Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
235000013601 eggs Nutrition 0.000 description 1
238000005538 encapsulation Methods 0.000 description 1
239000003344 environmental pollutant Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
210000003608 fece Anatomy 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000010440 gypsum Substances 0.000 description 1
229910052602 gypsum Inorganic materials 0.000 description 1
125000001475 halogen functional group Chemical group 0.000 description 1
231100001261 hazardous Toxicity 0.000 description 1
230000004886 head movement Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
229920000554 ionomer Polymers 0.000 description 1
QRXWMOHMRWLFEY-UHFFFAOYSA-N isoniazide Chemical compound NNC(=O)C1=CC=NC=C1 QRXWMOHMRWLFEY-UHFFFAOYSA-N 0.000 description 1
229910052622 kaolinite Inorganic materials 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
238000009533 lab test Methods 0.000 description 1
230000001418 larval effect Effects 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
239000003094 microcapsule Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
LMNZTLDVJIUSHT-UHFFFAOYSA-N phosmet Chemical compound C1=CC=C2C(=O)N(CSP(=S)(OC)OC)C(=O)C2=C1 LMNZTLDVJIUSHT-UHFFFAOYSA-N 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
231100000719 pollutant Toxicity 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000139 polyethylene terephthalate Polymers 0.000 description 1
239000005020 polyethylene terephthalate Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920002620 polyvinyl fluoride Polymers 0.000 description 1
229920000131 polyvinylidene Polymers 0.000 description 1
230000003389 potentiating effect Effects 0.000 description 1
239000004540 pour-on Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000002728 pyrethroid Substances 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000004627 regenerated cellulose Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
241000894007 species Species 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
230000004083 survival effect Effects 0.000 description 1
239000000725 suspension Substances 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)

CA000352319A 1980-05-21 1980-05-21 Compositions tiquicides synergiques Expired CA1142851A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA000352319A CA1142851A (fr)	1980-05-21	1980-05-21	Compositions tiquicides synergiques

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA000352319A CA1142851A (fr)	1980-05-21	1980-05-21	Compositions tiquicides synergiques

Publications (1)

Publication Number	Publication Date
CA1142851A true CA1142851A (fr)	1983-03-15

Family

ID=4116998

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000352319A Expired CA1142851A (fr)	1980-05-21	1980-05-21	Compositions tiquicides synergiques

Country Status (1)

Country	Link
CA (1)	CA1142851A (fr)

1980
- 1980-05-21 CA CA000352319A patent/CA1142851A/fr not_active Expired

Legal Events

Date	Code	Title	Description
2000-03-15	MKEX	Expiry

Publication	Publication Date	Title
US4171355A (en)	1979-10-16	Certain tickicidal pyrethroid mixtures and stabilizer therefor
EP0005826B1 (fr)	1985-09-11	Mélanges synergétiques de composés pyréthroides et leur préparation
US4362722A (en)	1982-12-07	Synergistic tickicidal compositions containing organophosphorus compounds and cyclopropane carboxylates
US4178384A (en)	1979-12-11	Pyrethroid insect repellent
IE47446B1 (en)	1984-03-21	Insecticidal and acaricidal compositions
CA2756649C (fr)	2017-11-14	Compositons de pesticide topique renfermant de l'azamethiphos et de la cypermethrine ou de la deltamethrine en vue de combattre les ectoparasites sur les poissons
EP1372396B1 (fr)	2009-01-21	Composition pesticide
DE3615035C2 (de)	1997-03-13	Neue Verwendung von Schädlingsbekämpfungsmitteln und Verfahren zur Bekämpfung von Küchenschaben
GB1592056A (en)	1981-07-01	Synergistic parasiticidal compositions
CA1142851A (fr)	1983-03-15	Compositions tiquicides synergiques
GB1583847A (en)	1981-02-04	Pesticidal compositions
EP0053100B1 (fr)	1984-09-19	Agents pesticides
JPS5946206A (ja)	1984-03-15	相乗性殺虫剤組成物
US4308262A (en)	1981-12-29	Pyrethroid pesticidal compositions
JPS6036403A (ja)	1985-02-25	混合殺虫組成物
GB1581277A (en)	1980-12-10	Pesticidal compositions
US4554270A (en)	1985-11-19	Pesticidal composition containing a synergistic combination of 3-hydroxymethylacrylic acid methyl ester dimethylthionophosphate and cypermethrin
GB2052264A (en)	1981-01-28	Ectoparasiticidal agents containing substituted phenoxy-benzyloxycarbonyl derivatives and (thio) phoshphoric acid esters, a process for the preparation and their use as estoparasiticides
KR840000837B1 (ko)	1984-06-19	살충성 조성물
US4132785A (en)	1979-01-02	Isopropyl parathion as an insecticide for treating soil
GB2079604A (en)	1982-01-27	Pesticidal composition
IE45143B1 (en)	1982-06-30	Improvements in or relating to pesticides
DE1966823B2 (de)	1980-08-28	Insecticide und acaricide Zubereitung auf Basis von Benzimidazolderivaten
DD202380A5 (de)	1983-09-14	Schaedlingsbekaempfungsmittel
DE3023873A1 (de)	1982-01-21	Pestizide mittel und ihre verwendung