SK207587A3 - Pesticidal agent - Google Patents

Pesticidal agent Download PDF

Info

Publication number: SK207587A3
Authority: SK; Slovakia
Prior art keywords: group; compound; alkyl; pesticide; pesticidal composition
Prior art date: 1986-03-31

Application number

SK2075-87A

Other languages

English (en)

Slovak (sk)

Other versions

SK278483B6 (en

Inventor

Herbert B Scher

Marius Rodson

Ronald L Morgan

Original Assignee

Stauffer Chemical Co

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.)

1986-03-31

Filing date

1987-03-26

Publication date

1997-07-09

1987-03-26 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1997-07-09 Publication of SK278483B6 publication Critical patent/SK278483B6/sk

1997-07-09 Publication of SK207587A3 publication Critical patent/SK207587A3/sk

Links

239000000203 mixture Substances 0.000 claims abstract description 61
239000000575 pesticide Substances 0.000 claims abstract description 29
231100000331 toxic Toxicity 0.000 claims abstract description 6
230000002588 toxic effect Effects 0.000 claims abstract description 6
239000002736 nonionic surfactant Substances 0.000 claims abstract description 5
150000001875 compounds Chemical class 0.000 claims description 21
230000000361 pesticidal effect Effects 0.000 claims description 21
239000004094 surface-active agent Substances 0.000 claims description 17
150000002903 organophosphorus compounds Chemical class 0.000 claims description 13
229910052760 oxygen Inorganic materials 0.000 claims description 9
-1 phenoxy, phenylthio Chemical group 0.000 claims description 9
230000002500 effect on skin Effects 0.000 claims description 7
125000001424 substituent group Chemical group 0.000 claims description 7
229910052717 sulfur Chemical group 0.000 claims description 5
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
239000002245 particle Substances 0.000 claims description 4
125000002071 phenylalkoxy group Chemical group 0.000 claims description 4
239000011593 sulfur Chemical group 0.000 claims description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 3
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 3
125000004093 cyano group Chemical group *C#N 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 2
JKTAIYGNOFSMCE-UHFFFAOYSA-N 2,3-di(nonyl)phenol Chemical group CCCCCCCCCC1=CC=CC(O)=C1CCCCCCCCC JKTAIYGNOFSMCE-UHFFFAOYSA-N 0.000 claims description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
239000001301 oxygen Substances 0.000 claims description 2
125000004660 phenylalkylthio group Chemical group 0.000 claims description 2
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
125000003342 alkenyl group Chemical group 0.000 claims 1
125000003302 alkenyloxy group Chemical group 0.000 claims 1
125000004414 alkyl thio group Chemical group 0.000 claims 1
125000002346 iodo group Chemical group I* 0.000 claims 1
229910052698 phosphorus Inorganic materials 0.000 claims 1
239000011574 phosphorus Substances 0.000 claims 1
239000003701 inert diluent Substances 0.000 abstract description 6
239000004927 clay Substances 0.000 description 20
238000012360 testing method Methods 0.000 description 15
KVGLBTYUCJYMND-UHFFFAOYSA-N fonofos Chemical compound CCOP(=S)(CC)SC1=CC=CC=C1 KVGLBTYUCJYMND-UHFFFAOYSA-N 0.000 description 12
241000283973 Oryctolagus cuniculus Species 0.000 description 10
230000007682 dermal toxicity Effects 0.000 description 10
231100000438 skin toxicity Toxicity 0.000 description 10
241001465754 Metazoa Species 0.000 description 9
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 9
239000008187 granular material Substances 0.000 description 9
239000004480 active ingredient Substances 0.000 description 7
230000004071 biological effect Effects 0.000 description 6
229920001223 polyethylene glycol Polymers 0.000 description 6
210000003491 skin Anatomy 0.000 description 6
239000000126 substance Substances 0.000 description 6
XLNZEKHULJKQBA-UHFFFAOYSA-N terbufos Chemical compound CCOP(=S)(OCC)SCSC(C)(C)C XLNZEKHULJKQBA-UHFFFAOYSA-N 0.000 description 6
230000001988 toxicity Effects 0.000 description 6
231100000419 toxicity Toxicity 0.000 description 6
239000002202 Polyethylene glycol Substances 0.000 description 5
235000013601 eggs Nutrition 0.000 description 5
238000000034 method Methods 0.000 description 5
238000002156 mixing Methods 0.000 description 5
BULVZWIRKLYCBC-UHFFFAOYSA-N phorate Chemical compound CCOP(=S)(OCC)SCSCC BULVZWIRKLYCBC-UHFFFAOYSA-N 0.000 description 5
239000002689 soil Substances 0.000 description 5
125000000217 alkyl group Chemical group 0.000 description 4
239000004359 castor oil Substances 0.000 description 4
235000019438 castor oil Nutrition 0.000 description 4
AWZOLILCOUMRDG-UHFFFAOYSA-N edifenphos Chemical compound C=1C=CC=CC=1SP(=O)(OCC)SC1=CC=CC=C1 AWZOLILCOUMRDG-UHFFFAOYSA-N 0.000 description 4
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
241000607479 Yersinia pestis Species 0.000 description 3
230000033228 biological regulation Effects 0.000 description 3
230000037396 body weight Effects 0.000 description 3
239000000969 carrier Substances 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
238000009472 formulation Methods 0.000 description 3
230000012010 growth Effects 0.000 description 3
230000000749 insecticidal effect Effects 0.000 description 3
239000002917 insecticide Substances 0.000 description 3
ATROHALUCMTWTB-WYMLVPIESA-N (z)-n-diethoxyphosphinothioyloxybenzenecarboximidoyl cyanide Chemical compound CCOP(=S)(OCC)O\N=C(/C#N)C1=CC=CC=C1 ATROHALUCMTWTB-WYMLVPIESA-N 0.000 description 2
RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
OKIJSNGRQAOIGZ-UHFFFAOYSA-N Butopyronoxyl Chemical compound CCCCOC(=O)C1=CC(=O)CC(C)(C)O1 OKIJSNGRQAOIGZ-UHFFFAOYSA-N 0.000 description 2
QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 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
241000489975 Diabrotica Species 0.000 description 2
RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
ANIAQSUBRGXWLS-UHFFFAOYSA-N Trichloronat Chemical compound CCOP(=S)(CC)OC1=CC(Cl)=C(Cl)C=C1Cl ANIAQSUBRGXWLS-UHFFFAOYSA-N 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
231100000293 acute skin toxicity Toxicity 0.000 description 2
239000002519 antifouling agent Substances 0.000 description 2
229960000892 attapulgite Drugs 0.000 description 2
239000011230 binding agent Substances 0.000 description 2
QGTYWWGEWOBMAK-UHFFFAOYSA-N chlormephos Chemical compound CCOP(=S)(OCC)SCCl QGTYWWGEWOBMAK-UHFFFAOYSA-N 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
230000007613 environmental effect Effects 0.000 description 2
KQTVWCSONPJJPE-UHFFFAOYSA-N etridiazole Chemical compound CCOC1=NC(C(Cl)(Cl)Cl)=NS1 KQTVWCSONPJJPE-UHFFFAOYSA-N 0.000 description 2
XDNBJTQLKCIJBV-UHFFFAOYSA-N fensulfothion Chemical compound CCOP(=S)(OCC)OC1=CC=C(S(C)=O)C=C1 XDNBJTQLKCIJBV-UHFFFAOYSA-N 0.000 description 2
BUYMVQAILCEWRR-UHFFFAOYSA-N naled Chemical compound COP(=O)(OC)OC(Br)C(Cl)(Cl)Br BUYMVQAILCEWRR-UHFFFAOYSA-N 0.000 description 2
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
229910052625 palygorskite Inorganic materials 0.000 description 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
PWYIUEFFPNVCMW-UHFFFAOYSA-N propaphos Chemical compound CCCOP(=O)(OCCC)OC1=CC=C(SC)C=C1 PWYIUEFFPNVCMW-UHFFFAOYSA-N 0.000 description 2
ZYHMJXZULPZUED-UHFFFAOYSA-N propargite Chemical compound C1=CC(C(C)(C)C)=CC=C1OC1C(OS(=O)OCC#C)CCCC1 ZYHMJXZULPZUED-UHFFFAOYSA-N 0.000 description 2
230000002829 reductive effect Effects 0.000 description 2
239000000243 solution Substances 0.000 description 2
241000894007 species Species 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
210000001519 tissue Anatomy 0.000 description 2
231100000167 toxic agent Toxicity 0.000 description 2
239000003440 toxic substance Substances 0.000 description 2
ZCVAOQKBXKSDMS-PVAVHDDUSA-N (+)-trans-(S)-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-PVAVHDDUSA-N 0.000 description 1
ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 1
SBNFWQZLDJGRLK-RTWAWAEBSA-N (1R)-trans-phenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-RTWAWAEBSA-N 0.000 description 1
125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 1
125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
125000006700 (C1-C6) alkylthio group Chemical group 0.000 description 1
GNEPLYVYORHREW-UHFFFAOYSA-N 1,1,3,3,6-pentamethyl-7-nitro-2h-inden-5-amine Chemical compound CC1=C(N)C=C2C(C)(C)CC(C)(C)C2=C1[N+]([O-])=O GNEPLYVYORHREW-UHFFFAOYSA-N 0.000 description 1
LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 description 1
JVGPVVUTUMQJKL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl thiocyanate Chemical compound CCCCOCCOCCSC#N JVGPVVUTUMQJKL-UHFFFAOYSA-N 0.000 description 1
KWGUFOITWDSNQY-UHFFFAOYSA-N Bromophos-ethyl Chemical group CCOP(=S)(OCC)OC1=CC(Cl)=C(Br)C=C1Cl KWGUFOITWDSNQY-UHFFFAOYSA-N 0.000 description 1
125000000882 C2-C6 alkenyl group Chemical group 0.000 description 1
RAPBNVDSDCTNRC-UHFFFAOYSA-N Chlorobenzilate Chemical compound C=1C=C(Cl)C=CC=1C(O)(C(=O)OCC)C1=CC=C(Cl)C=C1 RAPBNVDSDCTNRC-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
239000005769 Etridiazole Substances 0.000 description 1
PNVJTZOFSHSLTO-UHFFFAOYSA-N Fenthion Chemical compound COP(=S)(OC)OC1=CC=C(SC)C(C)=C1 PNVJTZOFSHSLTO-UHFFFAOYSA-N 0.000 description 1
241000238631 Hexapoda Species 0.000 description 1
240000008415 Lactuca sativa Species 0.000 description 1
235000003228 Lactuca sativa Nutrition 0.000 description 1
239000004166 Lanolin Substances 0.000 description 1
TZBPRYIIJAJUOY-UHFFFAOYSA-N Pirimiphos-ethyl Chemical group CCOP(=S)(OCC)OC1=CC(C)=NC(N(CC)CC)=N1 TZBPRYIIJAJUOY-UHFFFAOYSA-N 0.000 description 1
239000005924 Pirimiphos-methyl Substances 0.000 description 1
229920002043 Pluronic® L 35 Polymers 0.000 description 1
229920002066 Pluronic® P 65 Polymers 0.000 description 1
PNAAEIYEUKNTMO-UHFFFAOYSA-N S-Seven Chemical compound C=1C=CC=CC=1P(=S)(OCC)OC1=CC=C(Cl)C=C1Cl PNAAEIYEUKNTMO-UHFFFAOYSA-N 0.000 description 1
206010040840 Skin erosion Diseases 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
VXSIXFKKSNGRRO-MXOVTSAMSA-N [(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate;[(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl Chemical class CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1.CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VXSIXFKKSNGRRO-MXOVTSAMSA-N 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000002411 adverse Effects 0.000 description 1
239000003619 algicide Substances 0.000 description 1
239000003513 alkali Substances 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
229940024113 allethrin Drugs 0.000 description 1
239000000729 antidote Substances 0.000 description 1
229940075522 antidotes Drugs 0.000 description 1
230000008901 benefit Effects 0.000 description 1
229960001901 bioallethrin Drugs 0.000 description 1
230000031018 biological processes and functions Effects 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
SCKHCCSZFPSHGR-UHFFFAOYSA-N cyanophos Chemical compound COP(=S)(OC)OC1=CC=C(C#N)C=C1 SCKHCCSZFPSHGR-UHFFFAOYSA-N 0.000 description 1
230000034994 death Effects 0.000 description 1
210000004207 dermis Anatomy 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
229910003460 diamond Inorganic materials 0.000 description 1
239000010432 diamond Substances 0.000 description 1
FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
FAXIJTUDSBIMHY-UHFFFAOYSA-N diethoxy-(2-ethylsulfanylethoxy)-sulfanylidene-$l^{5}-phosphane;1-diethoxyphosphorylsulfanyl-2-ethylsulfanylethane Chemical compound CCOP(=O)(OCC)SCCSCC.CCOP(=S)(OCC)OCCSCC FAXIJTUDSBIMHY-UHFFFAOYSA-N 0.000 description 1
GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
SPCNPOWOBZQWJK-UHFFFAOYSA-N dimethoxy-(2-propan-2-ylsulfanylethylsulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound COP(=S)(OC)SCCSC(C)C SPCNPOWOBZQWJK-UHFFFAOYSA-N 0.000 description 1
238000002224 dissection Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
231100000290 environmental risk assessment Toxicity 0.000 description 1
210000002615 epidermis Anatomy 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
ULUJSLFWDQSXRS-UHFFFAOYSA-N ethenyl diethyl phosphate Chemical compound CCOP(=O)(OCC)OC=C ULUJSLFWDQSXRS-UHFFFAOYSA-N 0.000 description 1
RIZMRRKBZQXFOY-UHFFFAOYSA-N ethion Chemical compound CCOP(=S)(OCC)SCSP(=S)(OCC)OCC RIZMRRKBZQXFOY-UHFFFAOYSA-N 0.000 description 1
VJYFKVYYMZPMAB-UHFFFAOYSA-N ethoprophos Chemical compound CCCSP(=O)(OCC)SCCC VJYFKVYYMZPMAB-UHFFFAOYSA-N 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
238000003898 horticulture Methods 0.000 description 1
GBHRVZIGDIUCJB-UHFFFAOYSA-N hydrogenphosphite Chemical class OP([O-])[O-] GBHRVZIGDIUCJB-UHFFFAOYSA-N 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000002147 killing effect Effects 0.000 description 1
229940039717 lanolin Drugs 0.000 description 1
235000019388 lanolin Nutrition 0.000 description 1
231100000636 lethal dose Toxicity 0.000 description 1
238000005259 measurement Methods 0.000 description 1
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
239000003750 molluscacide Substances 0.000 description 1
230000002013 molluscicidal effect Effects 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 1
229960003536 phenothrin Drugs 0.000 description 1
229950001664 phoxim Drugs 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
QHOQHJPRIBSPCY-UHFFFAOYSA-N pirimiphos-methyl Chemical group CCN(CC)C1=NC(C)=CC(OP(=S)(OC)OC)=N1 QHOQHJPRIBSPCY-UHFFFAOYSA-N 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 1
229940070846 pyrethrins Drugs 0.000 description 1
239000002728 pyrethroid Substances 0.000 description 1
230000009467 reduction Effects 0.000 description 1
239000005871 repellent Substances 0.000 description 1
230000002940 repellent Effects 0.000 description 1
230000002441 reversible effect Effects 0.000 description 1
239000003128 rodenticide Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
239000010959 steel Substances 0.000 description 1
210000000434 stratum corneum Anatomy 0.000 description 1
239000000758 substrate Substances 0.000 description 1
XIUROWKZWPIAIB-UHFFFAOYSA-N sulfotep Chemical compound CCOP(=S)(OCC)OP(=S)(OCC)OCC XIUROWKZWPIAIB-UHFFFAOYSA-N 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
PPEZWDDRWXDXOQ-UHFFFAOYSA-N tributoxy(sulfanylidene)-$l^{5}-phosphane Chemical compound CCCCOP(=S)(OCCCC)OCCCC PPEZWDDRWXDXOQ-UHFFFAOYSA-N 0.000 description 1
230000035899 viability Effects 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/12—Powders or granules
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/22—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing aromatic radicals

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Agronomy & Crop Science (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

SK2075-87A 1986-03-31 1987-03-26 Pesticidal agent SK207587A3 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US84618386A	1986-03-31	1986-03-31

Publications (2)

Publication Number	Publication Date
SK278483B6 SK278483B6 (en)	1997-07-09
SK207587A3 true SK207587A3 (en)	1997-07-09

Family

ID=25297177

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK2075-87A SK207587A3 (en)	1986-03-31	1987-03-26	Pesticidal agent

Country Status (15)

Country	Link
EP (1)	EP0243694B1 (fr)
CN (1)	CN1021281C (fr)
AR (1)	AR241992A1 (fr)
AT (1)	ATE85184T1 (fr)
BR (1)	BR8701421A (fr)
CA (1)	CA1317875C (fr)
CZ (1)	CZ282064B6 (fr)
DE (1)	DE3783935T2 (fr)
DK (1)	DK163887A (fr)
ES (1)	ES2053461T3 (fr)
HU (1)	HU205825B (fr)
IL (1)	IL82049A (fr)
MY (1)	MY101710A (fr)
PH (1)	PH24021A (fr)
SK (1)	SK207587A3 (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH03167106A (ja) *	1989-11-28	1991-07-19	Nippon Tokushu Noyaku Seizo Kk	安定化された農薬組成物
US6646011B2 (en) *	1998-06-03	2003-11-11	Johnson & Johnson Consumer Companies, Inc.	Insect repellant compositions
US9206381B2 (en)	2011-09-21	2015-12-08	Ecolab Usa Inc.	Reduced misting alkaline cleaners using elongational viscosity modifiers
US20150141251A1 (en) *	2012-10-15	2015-05-21	Gowan Comercio Internacional E Servicos Limiada	Spontaneous self-forming mixed surfactant nano-emulsions from water insoluble pesticides in mixed water miscible solvents
US9637708B2 (en)	2014-02-14	2017-05-02	Ecolab Usa Inc.	Reduced misting and clinging chlorine-based hard surface cleaner
EP3719107B1 (fr)	2016-05-23	2024-08-07	Ecolab USA Inc.	Compositions acides de nettoyage, d'aseptisation et de désinfection à faible embuage par l'utilisation de polymères en émulsion d'eau dans l'huile à masse moléculaire élevée
US10392587B2 (en)	2016-05-23	2019-08-27	Ecolab Usa Inc.	Reduced misting alkaline and neutral cleaning, sanitizing, and disinfecting compositions via the use of high molecular weight water-in-oil emulsion polymers
WO2018160818A1 (fr)	2017-03-01	2018-09-07	Ecolab Usa Inc.	Assainisseurs et désinfectants à risques d'inhalation réduits par l'intermédiaire de polymères de poids moléculaire élevé
MX2022000454A (es)	2019-07-12	2022-04-18	Ecolab Usa Inc	Limpiador alcalino de niebla reducida mediante el uso de polímeros en emulsión solubles en álcali.

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4133878A (en) *	1975-12-22	1979-01-09	Mobil Oil Corporation	Stabilized organothiophosphorus formulations
IT1193914B (it) *	1980-02-06	1988-08-31	Montedison Spa	Formulazioni granulari di antiparassitari fosforici chimicamente stabili
DE3473987D1 (en) *	1983-07-22	1988-10-20	Stauffer Chemical Co	Pesticide compositions
US4603214A (en) *	1985-02-14	1986-07-29	Bayer Aktiengesellschaft	Agents for combating pests

1987
- 1987-03-04 PH PH34960A patent/PH24021A/en unknown
- 1987-03-09 MY MYPI87000256A patent/MY101710A/en unknown
- 1987-03-20 AR AR87307074A patent/AR241992A1/es active
- 1987-03-26 SK SK2075-87A patent/SK207587A3/sk unknown
- 1987-03-26 CZ CS872075A patent/CZ282064B6/cs not_active IP Right Cessation
- 1987-03-27 EP EP87104629A patent/EP0243694B1/fr not_active Expired - Lifetime
- 1987-03-27 ES ES87104629T patent/ES2053461T3/es not_active Expired - Lifetime
- 1987-03-27 DE DE8787104629T patent/DE3783935T2/de not_active Expired - Fee Related
- 1987-03-27 AT AT87104629T patent/ATE85184T1/de active
- 1987-03-27 BR BR8701421A patent/BR8701421A/pt not_active IP Right Cessation
- 1987-03-30 HU HU871362A patent/HU205825B/hu not_active IP Right Cessation
- 1987-03-30 IL IL82049A patent/IL82049A/xx not_active IP Right Cessation
- 1987-03-30 CA CA000533312A patent/CA1317875C/fr not_active Expired - Fee Related
- 1987-03-31 CN CN87102422A patent/CN1021281C/zh not_active Expired - Lifetime
- 1987-03-31 DK DK163887A patent/DK163887A/da not_active Application Discontinuation

Also Published As

Publication number	Publication date
DE3783935T2 (de)	1993-06-03
PH24021A (en)	1990-02-09
HU205825B (en)	1992-07-28
DK163887A (da)	1987-10-01
IL82049A0 (en)	1987-10-20
DE3783935D1 (de)	1993-03-18
ATE85184T1 (de)	1993-02-15
CN1021281C (zh)	1993-06-23
CN87102422A (zh)	1987-10-07
DK163887D0 (da)	1987-03-31
EP0243694A3 (en)	1990-05-16
CA1317875C (fr)	1993-05-18
SK278483B6 (en)	1997-07-09
CZ282064B6 (cs)	1997-05-14
MY101710A (en)	1992-01-17
CZ207587A3 (en)	1997-02-12
IL82049A (en)	1992-12-01
BR8701421A (pt)	1987-12-29
AR241992A1 (es)	1993-02-26
EP0243694B1 (fr)	1993-02-03
EP0243694A2 (fr)	1987-11-04
HUT46517A (en)	1988-11-28
ES2053461T3 (es)	1994-08-01

Publication	Publication Date	Title
JP3428112B2 (ja)	2003-07-22	複合殺ダニ剤組成物
US5120542A (en)	1992-06-09	Pesticide compositions and method
AU684627B2 (en)	1997-12-18	Microencapsulated compositon of chlorpyrifos or endosulfan
SK278483B6 (en)	1997-07-09	Pesticidal agent
US4933167A (en)	1990-06-12	Pesticide compositions
US2588969A (en)	1952-03-11	Certain acylamino-acrylates and-crotonates as insecticides
JPS5942646B2 (ja)	1984-10-16	忌避剤
US4215116A (en)	1980-07-29	Propoxylate toxicants
EP0134674B1 (fr)	1988-09-14	Compositions pesticides
JPS6241564B2 (fr)	1987-09-03
US4994261A (en)	1991-02-19	Pesticide compositions and method
GB1562908A (en)	1980-03-19	Insecticidal compostions
JPH0441406A (ja)	1992-02-12	ピレスロイド系化合物の安定剤及びピレスロイド系化合物の安定化方法
EP0091213A2 (fr)	1983-10-12	Compositions pesticides sous forme sèche pour le traitement des semences
CZ248594A3 (en)	1995-04-12	Pesticidal agents and application method thereof
HU188391B (en)	1986-04-28	Insecticide composition containing salicylic acid derivatives as activators
US4522825A (en)	1985-06-11	Acaricide compositions employing synergistic mixtures of 1-decyloxy-4-(7-oxa-4-octinyl)-oxy-benzene and propargite
CA1125655A (fr)	1982-06-15	Amido-amine toxique
US2745729A (en)	1956-05-15	Herbicidal composition
JP3465854B2 (ja)	2003-11-10	殺屋内塵性ダニ剤
JPH0120125B2 (fr)	1989-04-14
US3478153A (en)	1969-11-11	Method of protecting sheep from blowfly larvae
JP3349551B2 (ja)	2002-11-25	シロアリ防除剤
US2940896A (en)	1960-06-14	Quaternary ammonium and phosphoramide ester attractants and insect control therewith
JPS63270605A (ja)	1988-11-08	防蟻組成物