IL116148A - Complexible composition for insect control - Google Patents

Complexible composition for insect control

Info

Publication number: IL116148A
Authority: IL; Israel
Prior art keywords: composition according; foregoing; insects; solvent; polar solvent
Prior art date: 1994-11-30

Application number

IL11614895A

Other languages

English (en)

Hebrew (he)

Other versions

IL116148A0 (en

Inventor

Takaaki Mizutani

Michihiko Ikeda

Hiroshi Kodama

Masakazu Shibayama

Original Assignee

Rhone Poulenc Agrochimie

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.)

1994-11-30

Filing date

1995-11-27

Publication date

2001-03-19

1995-11-27 Application filed by Rhone Poulenc Agrochimie filed Critical Rhone Poulenc Agrochimie

1996-01-31 Publication of IL116148A0 publication Critical patent/IL116148A0/xx

2001-03-19 Publication of IL116148A publication Critical patent/IL116148A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 64
241000238631 Hexapoda Species 0.000 title claims abstract description 28
239000002798 polar solvent Substances 0.000 claims abstract description 20
150000001875 compounds Chemical class 0.000 claims abstract description 18
239000004480 active ingredient Substances 0.000 claims abstract description 12
239000003995 emulsifying agent Substances 0.000 claims abstract description 12
229910052736 halogen Inorganic materials 0.000 claims abstract description 10
239000002728 pyrethroid Substances 0.000 claims abstract description 9
150000002367 halogens Chemical group 0.000 claims abstract description 7
239000003021 water soluble solvent Substances 0.000 claims abstract description 7
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 3
-1 glycol ethers Chemical class 0.000 claims description 22
241000256602 Isoptera Species 0.000 claims description 17
239000006260 foam Substances 0.000 claims description 14
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
239000004088 foaming agent Substances 0.000 claims description 11
238000000034 method Methods 0.000 claims description 11
239000002904 solvent Substances 0.000 claims description 10
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 claims description 9
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 9
239000013078 crystal Substances 0.000 claims description 8
239000007788 liquid Substances 0.000 claims description 8
241001465754 Metazoa Species 0.000 claims description 7
241000607479 Yersinia pestis Species 0.000 claims description 7
239000003849 aromatic solvent Substances 0.000 claims description 7
239000003381 stabilizer Substances 0.000 claims description 7
241000239223 Arachnida Species 0.000 claims description 6
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 5
YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 4
241000238876 Acari Species 0.000 claims description 4
239000005874 Bifenthrin Substances 0.000 claims description 4
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 4
WPPOGHDFAVQKLN-UHFFFAOYSA-N N-Octyl-2-pyrrolidone Chemical compound CCCCCCCCN1CCCC1=O WPPOGHDFAVQKLN-UHFFFAOYSA-N 0.000 claims description 4
239000000654 additive Substances 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 claims description 4
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 claims description 4
125000001188 haloalkyl group Chemical group 0.000 claims description 4
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 claims description 4
HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 claims description 4
241000282472 Canis lupus familiaris Species 0.000 claims description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
241000282326 Felis catus Species 0.000 claims description 3
INISTDXBRIBGOC-CGAIIQECSA-N [cyano-(3-phenoxyphenyl)methyl] (2s)-2-[2-chloro-4-(trifluoromethyl)anilino]-3-methylbutanoate Chemical compound N([C@@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-CGAIIQECSA-N 0.000 claims description 3
125000000129 anionic group Chemical group 0.000 claims description 3
229960001591 cyfluthrin Drugs 0.000 claims description 3
QQODLKZGRKWIFG-QSFXBCCZSA-N cyfluthrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-QSFXBCCZSA-N 0.000 claims description 3
XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 claims description 3
229940075557 diethylene glycol monoethyl ether Drugs 0.000 claims description 3
YREQHYQNNWYQCJ-UHFFFAOYSA-N etofenprox Chemical compound C1=CC(OCC)=CC=C1C(C)(C)COCC1=CC=CC(OC=2C=CC=CC=2)=C1 YREQHYQNNWYQCJ-UHFFFAOYSA-N 0.000 claims description 3
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 claims description 2
CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 claims description 2
VEMKTZHHVJILDY-PMACEKPBSA-N (5-benzylfuran-3-yl)methyl (1r,3s)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-PMACEKPBSA-N 0.000 claims description 2
ZFHGXWPMULPQSE-SZGBIDFHSA-N (Z)-(1S)-cis-tefluthrin Chemical compound FC1=C(F)C(C)=C(F)C(F)=C1COC(=O)[C@@H]1C(C)(C)[C@@H]1\C=C(/Cl)C(F)(F)F ZFHGXWPMULPQSE-SZGBIDFHSA-N 0.000 claims description 2
AXTGDCSMTYGJND-UHFFFAOYSA-N 1-dodecylazepan-2-one Chemical compound CCCCCCCCCCCCN1CCCCCC1=O AXTGDCSMTYGJND-UHFFFAOYSA-N 0.000 claims description 2
NJPQAIBZIHNJDO-UHFFFAOYSA-N 1-dodecylpyrrolidin-2-one Chemical compound CCCCCCCCCCCCN1CCCC1=O NJPQAIBZIHNJDO-UHFFFAOYSA-N 0.000 claims description 2
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 claims description 2
DJCYDDALXPHSHR-UHFFFAOYSA-N 2-(2-propoxyethoxy)ethanol Chemical compound CCCOCCOCCO DJCYDDALXPHSHR-UHFFFAOYSA-N 0.000 claims description 2
COBPKKZHLDDMTB-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethanol Chemical compound CCCCOCCOCCOCCO COBPKKZHLDDMTB-UHFFFAOYSA-N 0.000 claims description 2
WFSMVVDJSNMRAR-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]ethanol Chemical compound CCOCCOCCOCCO WFSMVVDJSNMRAR-UHFFFAOYSA-N 0.000 claims description 2
KCBPVRDDYVJQHA-UHFFFAOYSA-N 2-[2-(2-propoxyethoxy)ethoxy]ethanol Chemical compound CCCOCCOCCOCCO KCBPVRDDYVJQHA-UHFFFAOYSA-N 0.000 claims description 2
239000005892 Deltamethrin Substances 0.000 claims description 2
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 2
WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 2
241000258242 Siphonaptera Species 0.000 claims description 2
239000005939 Tefluthrin Substances 0.000 claims description 2
229940024113 allethrin Drugs 0.000 claims description 2
230000015572 biosynthetic process Effects 0.000 claims description 2
238000009835 boiling Methods 0.000 claims description 2
229930188620 butyrolactone Natural products 0.000 claims description 2
230000000295 complement effect Effects 0.000 claims description 2
LSFUGNKKPMBOMG-UHFFFAOYSA-N cycloprothrin Chemical compound ClC1(Cl)CC1(C=1C=CC=CC=1)C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 LSFUGNKKPMBOMG-UHFFFAOYSA-N 0.000 claims description 2
ZXQYGBMAQZUVMI-UNOMPAQXSA-N cyhalothrin Chemical compound CC1(C)C(\C=C(/Cl)C(F)(F)F)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-UNOMPAQXSA-N 0.000 claims description 2
229960002483 decamethrin Drugs 0.000 claims description 2
OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 claims description 2
229940028356 diethylene glycol monobutyl ether Drugs 0.000 claims description 2
150000002191 fatty alcohols Chemical class 0.000 claims description 2
JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 claims description 2
229960000490 permethrin Drugs 0.000 claims description 2
RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 claims description 2
229960003536 phenothrin Drugs 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
229940108410 resmethrin Drugs 0.000 claims description 2
VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 claims description 2
HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 claims description 2
229960005199 tetramethrin Drugs 0.000 claims description 2
YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 claims description 2
JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 claims description 2
PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 claims description 2
NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 claims 2
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 claims 1
239000005946 Cypermethrin Substances 0.000 claims 1
VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 claims 1
230000037396 body weight Effects 0.000 claims 1
229960005424 cypermethrin Drugs 0.000 claims 1
KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 claims 1
150000002170 ethers Chemical class 0.000 claims 1
XQUXKZZNEFRCAW-UHFFFAOYSA-N fenpropathrin Chemical compound CC1(C)C(C)(C)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 XQUXKZZNEFRCAW-UHFFFAOYSA-N 0.000 claims 1
GBIHOLCMZGAKNG-CGAIIQECSA-N flucythrinate Chemical compound O=C([C@@H](C(C)C)C=1C=CC(OC(F)F)=CC=1)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 GBIHOLCMZGAKNG-CGAIIQECSA-N 0.000 claims 1
125000004438 haloalkoxy group Chemical group 0.000 claims 1
PZYDAVFRVJXFHS-UHFFFAOYSA-N n-cyclohexyl-2-pyrrolidone Chemical compound O=C1CCCN1C1CCCCC1 PZYDAVFRVJXFHS-UHFFFAOYSA-N 0.000 claims 1
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125000005843 halogen group Chemical group 0.000 abstract description 5
125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 2
HCMJWOGOISXSDL-UHFFFAOYSA-N (2-isothiocyanato-1-phenylethyl)benzene Chemical group C=1C=CC=CC=1C(CN=C=S)C1=CC=CC=C1 HCMJWOGOISXSDL-UHFFFAOYSA-N 0.000 abstract 1
125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 1
229910052739 hydrogen Inorganic materials 0.000 abstract 1
239000001257 hydrogen Substances 0.000 abstract 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
125000001424 substituent group Chemical group 0.000 abstract 1
238000002425 crystallisation Methods 0.000 description 9
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238000005187 foaming Methods 0.000 description 6
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QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 5
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238000009472 formulation Methods 0.000 description 5
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238000010790 dilution Methods 0.000 description 4
239000012895 dilution Substances 0.000 description 4
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239000011575 calcium Substances 0.000 description 3
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QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
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230000000996 additive effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229940077388 benzenesulfonate Drugs 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
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MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical class C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000004210 ether based solvent Substances 0.000 description 1
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
230000003648 hair appearance Effects 0.000 description 1
239000008233 hard water Substances 0.000 description 1
125000003454 indenyl group Chemical class C1(C=CC2=CC=CC=C12)* 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
LZGUHMNOBNWABZ-UHFFFAOYSA-N n-nitro-n-phenylnitramide Chemical compound [O-][N+](=O)N([N+]([O-])=O)C1=CC=CC=C1 LZGUHMNOBNWABZ-UHFFFAOYSA-N 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
229960005323 phenoxyethanol Drugs 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical class C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 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
239000002023 wood Substances 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
- 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
- A01N25/02—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 liquids as carriers, diluents or solvents
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Environmental Sciences (AREA)
Zoology (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Veterinary Medicine (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Public Health (AREA)
Chemical & Material Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Organic Chemistry (AREA)
Animal Behavior & Ethology (AREA)
Tropical Medicine & Parasitology (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Saccharide Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

IL11614895A 1994-11-30 1995-11-27 Complexible composition for insect control IL116148A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP32164594		1994-11-30

Publications (2)

Publication Number	Publication Date
IL116148A0 IL116148A0 (en)	1996-01-31
IL116148A true IL116148A (en)	2001-03-19

Family

ID=18134819

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL11614895A IL116148A (en)	1994-11-30	1995-11-27	Complexible composition for insect control

Country Status (19)

Country	Link
US (1)	US6066660A (de)
EP (1)	EP0794701B1 (de)
KR (1)	KR100404646B1 (de)
CN (1)	CN1074647C (de)
AT (1)	ATE189100T1 (de)
AU (1)	AU715579B2 (de)
BR (1)	BR9510169A (de)
CA (1)	CA2200603C (de)
CO (1)	CO4650016A1 (de)
DE (1)	DE69514828T2 (de)
DK (1)	DK0794701T3 (de)
ES (1)	ES2141396T3 (de)
GR (1)	GR3032487T3 (de)
IL (1)	IL116148A (de)
NZ (1)	NZ297003A (de)
PT (1)	PT794701E (de)
TR (1)	TR199501522A2 (de)
WO (1)	WO1996016543A2 (de)
ZA (1)	ZA9510186B (de)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6426333B1 (en)	1996-09-19	2002-07-30	Merial	Spot-on formulations for combating parasites
FR2753377B1 (fr)	1996-09-19	1999-09-24	Rhone Merieux	Nouvelle association parasiticide a base de 1-n-phenylpyra- zoles et de lactones macrocycliques endectocides
IL116147A (en) *	1994-11-30	2002-05-23	Aventis Cropscience Sa	Complexible composition for insect control
FR2735952B1 (fr)	1995-06-29	1997-08-01	Rhone Poulenc Agrochimie	Procede de controle d'une population d'insectes sociaux
JPH0987111A (ja) *	1995-09-27	1997-03-31	Sumitomo Chem Co Ltd	害虫駆除用毒餌剤
FR2739255B1 (fr)	1995-09-29	1998-09-04	Rhone Merieux	Composition antiparasitaire pour le traitement et la protection des animaux de compagnie
US6998131B2 (en)	1996-09-19	2006-02-14	Merial Limited	Spot-on formulations for combating parasites
JP3489401B2 (ja) *	1997-07-31	2004-01-19	住友化学工業株式会社	殺虫剤組成物
JPH11240809A (ja) *	1998-02-24	1999-09-07	Nippon Nohyaku Co Ltd	土壌処理用白蟻防除組成物
EP0963695A1 (de) *	1998-06-08	1999-12-15	Rhone Poulenc Agro	Insektizides Verfahren
JP4338837B2 (ja) *	1999-08-09	2009-10-07	フマキラー株式会社	殺虫剤組成物
FR2805971B1 (fr) *	2000-03-08	2004-01-30	Aventis Cropscience Sa	Procedes de traitement et/ou de protection des cultures contre les arthropodes et compositions utiles pour de tels procedes
RU2176879C1 (ru) *	2000-05-31	2001-12-20	Кольцов Николай Семенович	Инсектицидная композиция и способ борьбы с насекомыми
AU2008200430B2 (en) *	2001-07-25	2011-04-21	Syngenta Limited	Insecticidal mixture containing gamma-cyhalothrin
GB0118137D0 (en) *	2001-07-25	2001-09-19	Syngenta Ltd	Insecticidal mixture
US20050245582A1 (en) *	2002-09-12	2005-11-03	The Hartz Mountain Corporation	High concentration topical insecticides containing pyrethroids
EP1890767A2 (de) *	2005-05-27	2008-02-27	Pfizer Products Inc.	Kombinationstherapie zur behandlung von fettleibigkeit oder aufrechterhaltung des gewichtverlusts
CN1903029A (zh) *	2005-07-27	2007-01-31	拜尔农作物科学有限公司	微乳剂
DE102006061538A1 (de) *	2006-12-27	2008-07-03	Bayer Healthcare Ag	Kombinationsprodukt zur Bekämpfung von Parasiten an Tieren
AU2014271256B2 (en) *	2008-12-09	2016-12-15	Fmc Australasia Pty Ltd	Synergistic methods for control of pests
US20100144819A1 (en) *	2008-12-09	2010-06-10	Fmc Australasia Pty. Ltd.	Synergistic Methods for Control of Pests
AU2010215126B2 (en)	2009-02-20	2013-12-19	Deepak Pranjivandas Shah	A novel water dispersible granular composition
JO3626B1 (ar)	2012-02-23	2020-08-27	Merial Inc	تركيبات موضعية تحتوي على فيبرونيل و بيرميثرين و طرق استخدامها
CN102640747B (zh) *	2012-04-25	2013-11-06	南京太化化工有限公司	氯氰菊酯专用乳化剂及其乳油制剂
KR101250424B1 (ko) *	2012-09-17	2013-04-08	서진문화유산(주)	목재톱밥을 주요 성분으로 함유하는 흰개미 유인 및 살충용 조성물
US8993613B2 (en) *	2013-04-17	2015-03-31	The Hartz Mountain Corporation	Ectoparasiticidal formulations
EP3051944B1 (de)	2013-09-30	2023-11-01	FMC Corporation	Verfahren zur abgabe eines agrochemischen wirkstoffs
UY36181A (es)	2014-06-24	2016-09-30	Fmc Corp	Formulaciones de espumas y concentrados emulsionables
KR20180098320A (ko)	2015-12-23	2018-09-03	에프엠씨 코포레이션	고랑에서의 종자의 현장 처리
CN105557746B (zh) *	2015-12-29	2018-04-20	南京华洲药业有限公司	一种含乙螨唑与硅醚菊酯的增效杀虫组合物及其应用
CN110663685B (zh) *	2019-10-23	2021-10-12	扬州大学	一种介孔二氧化硅负载ppte的纳米农药制剂
CN111328818A (zh) *	2020-03-31	2020-06-26	厦门可灵有害生物防治有限公司	一种灭白蚁的混合物、用于制作灭白蚁的混合物的方法及灭白蚁的方法
CN118450798A (zh)	2021-12-16	2024-08-06	联合工业公司	即用型屏障和击倒杀有害生物剂

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP3355736B2 (ja) *	1993-12-20	2002-12-09	住友化学工業株式会社	殺虫、殺ダニ剤組成物
GB1473105A (de) *	1973-08-10	1977-05-11
IT1131750B (it) *	1980-06-06	1986-06-25	Montedison Spa	Formulazioni stabili di n-(3,4-diclorofenil)-n'metossi-n'-metilurea (linorun) e 2,6-dinitor-n,n-dipropil-4-trifluoro metilanilina (trifluralin) in emulsione
FR2498201A2 (fr) *	1980-06-11	1982-07-23	Roussel Uclaf	Compositions stables a la lumiere contenant des composes pyrethrinoides et des colorants
US5232940A (en) *	1985-12-20	1993-08-03	Hatton Leslie R	Derivatives of N-phenylpyrazoles
GB8713768D0 (en) *	1987-06-12	1987-07-15	May & Baker Ltd	Compositions of matter
DE4013523A1 (de) *	1990-04-27	1991-10-31	Bayer Ag	Verwendung von n-alkyl-lactamen als kristallisationsinhibitoren
IL99161A (en) *	1990-08-17	1996-11-14	Takeda Chemical Industries Ltd	History of guanidine A process for their preparation and preparations from pesticides that contain them
GB9120641D0 (en) *	1991-09-27	1991-11-06	Ici Plc	Heterocyclic compounds
JP2994182B2 (ja) *	1992-07-23	1999-12-27	石原産業株式会社	アミド系化合物又はその塩、それらの製造方法及びそれらを含有する有害動物防除剤
US5439683A (en) *	1992-10-09	1995-08-08	Rhone-Poulenc Inc.	Paddy rice treatment
GB9306184D0 (en) *	1993-03-25	1993-05-19	Zeneca Ltd	Heteroaromatic compounds
JP2766848B2 (ja) *	1993-10-26	1998-06-18	三井化学株式会社	フラニル系殺虫剤
BR9507118A (pt) *	1994-02-27	1997-08-12	Rhone Paulenc Agrochimie	Composição pesticida método para controle e prevenção de cupins método para controle de cupins e método para controle de pestes em animais
FR2721800B1 (fr) *	1994-07-01	1997-12-26	Roussel Uclaf	Nouveaux concentres emulsionnables renfermant un u plussieurs pesticides

1995
- 1995-11-27 IL IL11614895A patent/IL116148A/en not_active IP Right Cessation
- 1995-11-29 AU AU41765/96A patent/AU715579B2/en not_active Ceased
- 1995-11-29 CO CO95056734A patent/CO4650016A1/es unknown
- 1995-11-29 DK DK95940254T patent/DK0794701T3/da active
- 1995-11-29 AT AT95940254T patent/ATE189100T1/de active
- 1995-11-29 BR BR9510169A patent/BR9510169A/pt not_active IP Right Cessation
- 1995-11-29 DE DE69514828T patent/DE69514828T2/de not_active Expired - Lifetime
- 1995-11-29 EP EP95940254A patent/EP0794701B1/de not_active Expired - Lifetime
- 1995-11-29 WO PCT/EP1995/004684 patent/WO1996016543A2/en not_active Ceased
- 1995-11-29 NZ NZ297003A patent/NZ297003A/xx not_active IP Right Cessation
- 1995-11-29 KR KR1019970702375A patent/KR100404646B1/ko not_active Expired - Fee Related
- 1995-11-29 ES ES95940254T patent/ES2141396T3/es not_active Expired - Lifetime
- 1995-11-29 CA CA2200603A patent/CA2200603C/en not_active Expired - Lifetime
- 1995-11-29 PT PT794701T patent/PT794701E/pt unknown
- 1995-11-29 CN CN95196455A patent/CN1074647C/zh not_active Expired - Lifetime
- 1995-11-30 TR TR95/01522A patent/TR199501522A2/xx unknown
- 1995-11-30 ZA ZA9510186A patent/ZA9510186B/xx unknown
1998
- 1998-12-08 US US09/207,571 patent/US6066660A/en not_active Expired - Lifetime
2000
- 2000-01-27 GR GR990402500T patent/GR3032487T3/el unknown

Also Published As

Publication number	Publication date
CN1169655A (zh)	1998-01-07
HK1002947A1 (en)	1998-09-30
ES2141396T3 (es)	2000-03-16
DK0794701T3 (da)	2000-04-17
WO1996016543A2 (en)	1996-06-06
GR3032487T3 (en)	2000-05-31
BR9510169A (pt)	1997-10-14
ZA9510186B (en)	1996-06-11
WO1996016543A3 (en)	1996-08-29
DE69514828T2 (de)	2000-08-17
DE69514828D1 (de)	2000-03-02
CA2200603C (en)	2011-01-25
US6066660A (en)	2000-05-23
EP0794701B1 (de)	2000-01-26
CN1074647C (zh)	2001-11-14
AU4176596A (en)	1996-06-19
MX9703587A (es)	1997-10-31
EP0794701A2 (de)	1997-09-17
TR199501522A2 (tr)	1996-07-21
NZ297003A (en)	1999-05-28
PT794701E (pt)	2000-04-28
CA2200603A1 (en)	1996-06-06
KR970705925A (ko)	1997-11-03
ATE189100T1 (de)	2000-02-15
AU715579B2 (en)	2000-02-03
KR100404646B1 (ko)	2004-02-14
IL116148A0 (en)	1996-01-31
CO4650016A1 (es)	1998-09-03

Legal Events

Date	Code	Title
2001-07-24	FF	Patent granted
2001-10-31	KB	Patent renewed
2002-02-10	KB	Patent renewed
2006-02-05	KB	Patent renewed
2010-05-17	KB	Patent renewed
2013-12-31	KB	Patent renewed
2016-06-30	EXP	Patent expired

Publication	Publication Date	Title
AU715579B2 (en)	2000-02-03	Emulsifiable composition for the control of insects
AU709475B2 (en)	1999-08-26	Emulsifiable composition for the control of insects
US5612047A (en)	1997-03-18	Pesticidal microemulsion formulation
US6296864B1 (en)	2001-10-02	Pesticidal composition
MXPA97003588A (en)	1998-07-03	Emulsifiable composition for insec control
US4940729A (en)	1990-07-10	Pesticidal formulations
JPH08225414A (ja)	1996-09-03	白蟻類防除用乳化性組成物及びその使用方法
US6090751A (en)	2000-07-18	Emulsifiable concentrate comprising an insecticidal 1-arylpyrazole
JP3838661B2 (ja)	2006-10-25	昆虫類防除用の乳化性組成物
CS195339B2 (en)	1980-01-31	Synergic insecticide and acaricide
RU2125798C1 (ru)	1999-02-10	Инсектицидная композиция, способ борьбы с насекомыми
HK1002947B (en)	2001-02-02	Emulsifiable composition for the control of insects
JP3954649B2 (ja)	2007-08-08	昆虫類防除用の乳化性組成物
MXPA97003587A (en)	1998-07-03	Emulsified composition for deinsec control
TW316838B (de)	1997-10-01
HK1002946B (en)	2001-02-02	Emulsifiable composition for the control of insects
KR20030037989A (ko)	2003-05-16	사이로마진과 델타메트린을 유효성분으로 하는 살충제조성물