LU82761A1 - Compositions insecticides liquides contenant des pyrethroides synthetiques - Google Patents

Compositions insecticides liquides contenant des pyrethroides synthetiques Download PDF

Info

Publication number: LU82761A1
Authority: LU; Luxembourg
Prior art keywords: compositions according; phenoxy; benzyl ester; vehicle; cyano
Prior art date: 1979-09-12

Application number

LU82761A

Other languages

English (en)

French (fr)

Inventor

A Longoni

Moro A Dal

F Pinamonti

Original Assignee

Montedison Spa

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.)

1979-09-12

Filing date

1980-09-10

Publication date

1981-04-17

1980-09-10 Application filed by Montedison Spa filed Critical Montedison Spa

1981-04-17 Publication of LU82761A1 publication Critical patent/LU82761A1/fr

Links

239000000203 mixture Substances 0.000 title claims description 124
VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 title claims description 15
239000002917 insecticide Substances 0.000 title description 7
239000007788 liquid Substances 0.000 title description 5
239000003981 vehicle Substances 0.000 claims description 31
239000004094 surface-active agent Substances 0.000 claims description 27
-1 R3 = H Chemical class 0.000 claims description 22
239000002728 pyrethroid Substances 0.000 claims description 21
239000002904 solvent Substances 0.000 claims description 20
235000015112 vegetable and seed oil Nutrition 0.000 claims description 17
239000008158 vegetable oil Substances 0.000 claims description 17
239000004480 active ingredient Substances 0.000 claims description 16
235000021122 unsaturated fatty acids Nutrition 0.000 claims description 13
150000004670 unsaturated fatty acids Chemical class 0.000 claims description 13
229910052736 halogen Inorganic materials 0.000 claims description 12
150000002367 halogens Chemical class 0.000 claims description 12
239000000839 emulsion Substances 0.000 claims description 11
230000000749 insecticidal effect Effects 0.000 claims description 10
238000000034 method Methods 0.000 claims description 10
239000002253 acid Substances 0.000 claims description 9
206010061217 Infestation Diseases 0.000 claims description 8
239000003963 antioxidant agent Substances 0.000 claims description 8
125000005456 glyceride group Chemical group 0.000 claims description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
239000012963 UV stabilizer Substances 0.000 claims description 5
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 4
UOHMMEJUHBCKEE-UHFFFAOYSA-N prehnitene Chemical compound CC1=CC=C(C)C(C)=C1C UOHMMEJUHBCKEE-UHFFFAOYSA-N 0.000 claims description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
230000003078 antioxidant effect Effects 0.000 claims description 3
150000002148 esters Chemical class 0.000 claims description 3
239000003381 stabilizer Substances 0.000 claims description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
229920002554 vinyl polymer Polymers 0.000 claims description 3
241000238631 Hexapoda Species 0.000 claims description 2
NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Polymers CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 claims description 2
NWGKJDSIEKMTRX-MDZDMXLPSA-N Sorbitan oleate Polymers CCCCCCCC\C=C\CCCCCCCC(=O)OCC(O)C1OCC(O)C1O NWGKJDSIEKMTRX-MDZDMXLPSA-N 0.000 claims description 2
NWGKJDSIEKMTRX-BFWOXRRGSA-N [(2r)-2-[(3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] (z)-octadec-9-enoate Polymers CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)C1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-BFWOXRRGSA-N 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 claims description 2
239000000428 dust Substances 0.000 claims description 2
239000008187 granular material Substances 0.000 claims description 2
239000000843 powder Substances 0.000 claims description 2
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 claims 2
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims 2
HVUMOYIDDBPOLL-UHFFFAOYSA-N 2-(3,4-Dihydroxyoxolan-2-yl)-2-hydroxyethyl octadecanoate Polymers CCCCCCCCCCCCCCCCCC(=O)OCC(O)C1OCC(O)C1O HVUMOYIDDBPOLL-UHFFFAOYSA-N 0.000 claims 1
HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Polymers CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 claims 1
HVUMOYIDDBPOLL-QNECDRBKSA-N [(2r)-2-[(3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] octadecanoate Polymers CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)C1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-QNECDRBKSA-N 0.000 claims 1
HVUMOYIDDBPOLL-XGKPLOKHSA-N [2-[(2r,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] octadecanoate Polymers CCCCCCCCCCCCCCCCCC(=O)OCC(O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XGKPLOKHSA-N 0.000 claims 1
HVUMOYIDDBPOLL-IIZJTUPISA-N [2-[(2r,3s,4r)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] octadecanoate Polymers CCCCCCCCCCCCCCCCCC(=O)OCC(O)[C@H]1OC[C@@H](O)[C@@H]1O HVUMOYIDDBPOLL-IIZJTUPISA-N 0.000 claims 1
239000000654 additive Substances 0.000 claims 1
239000012965 benzophenone Substances 0.000 claims 1
239000007800 oxidant agent Substances 0.000 claims 1
230000000087 stabilizing effect Effects 0.000 claims 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
239000008096 xylene Substances 0.000 claims 1
241000196324 Embryophyta Species 0.000 description 13
239000000470 constituent Substances 0.000 description 10
235000014113 dietary fatty acids Nutrition 0.000 description 8
239000000194 fatty acid Substances 0.000 description 8
229930195729 fatty acid Natural products 0.000 description 8
150000004665 fatty acids Chemical class 0.000 description 8
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230000000694 effects Effects 0.000 description 7
238000009472 formulation Methods 0.000 description 7
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CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
239000011575 calcium Substances 0.000 description 6
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 description 5
230000002688 persistence Effects 0.000 description 5
230000002085 persistent effect Effects 0.000 description 5
230000002195 synergetic effect Effects 0.000 description 5
235000019486 Sunflower oil Nutrition 0.000 description 4
240000004460 Tanacetum coccineum Species 0.000 description 4
ROVGZAWFACYCSP-MQBLHHJJSA-N [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 Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-MQBLHHJJSA-N 0.000 description 4
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239000003921 oil Substances 0.000 description 3
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ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
238000007539 photo-oxidation reaction Methods 0.000 description 3
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
240000008067 Cucumis sativus Species 0.000 description 2
239000005946 Cypermethrin Substances 0.000 description 2
206010015946 Eye irritation Diseases 0.000 description 2
235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
241000124008 Mammalia Species 0.000 description 2
239000005642 Oleic acid Substances 0.000 description 2
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
240000003768 Solanum lycopersicum Species 0.000 description 2
244000061456 Solanum tuberosum Species 0.000 description 2
241000256248 Spodoptera Species 0.000 description 2
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 2
239000003849 aromatic solvent Substances 0.000 description 2
230000004071 biological effect Effects 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
239000004359 castor oil Substances 0.000 description 2
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229960005424 cypermethrin Drugs 0.000 description 2
229940079593 drug Drugs 0.000 description 2
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ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 2
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 2
238000005286 illumination Methods 0.000 description 2
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
239000002480 mineral oil Substances 0.000 description 2
239000000575 pesticide Substances 0.000 description 2
230000000885 phytotoxic effect Effects 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 2
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239000000725 suspension Substances 0.000 description 2
239000008399 tap water Substances 0.000 description 2
235000020679 tap water Nutrition 0.000 description 2
150000003626 triacylglycerols Chemical class 0.000 description 2
PRQBZVSKZHRPSZ-UHFFFAOYSA-N (2-hydroxyphenyl)-(4-octoxyphenyl)methanone Chemical compound C1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1O PRQBZVSKZHRPSZ-UHFFFAOYSA-N 0.000 description 1
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Polymers OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
RLLPVAHGXHCWKJ-IEBWSBKVSA-N (3-phenoxyphenyl)methyl (1s,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-IEBWSBKVSA-N 0.000 description 1
OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
CMCBDXRRFKYBDG-UHFFFAOYSA-N 1-dodecoxydodecane Chemical compound CCCCCCCCCCCCOCCCCCCCCCCCC CMCBDXRRFKYBDG-UHFFFAOYSA-N 0.000 description 1
PDOBSLHNWIVQJX-UHFFFAOYSA-N 1-ethenylcyclopropane-1-carboxylic acid Chemical compound OC(=O)C1(C=C)CC1 PDOBSLHNWIVQJX-UHFFFAOYSA-N 0.000 description 1
RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Polymers CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
JNYAEWCLZODPBN-UHFFFAOYSA-N 2-(1,2-dihydroxyethyl)oxolane-3,4-diol Polymers OCC(O)C1OCC(O)C1O JNYAEWCLZODPBN-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
VTJMSIIXXKNIDJ-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-methylbutyric acid Chemical compound CC(C)C(C(O)=O)C1=CC=C(Cl)C=C1 VTJMSIIXXKNIDJ-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
NPSJHQMIVNJLNN-UHFFFAOYSA-N 2-ethylhexyl 4-nitrobenzoate Chemical compound CCCCC(CC)COC(=O)C1=CC=C([N+]([O-])=O)C=C1 NPSJHQMIVNJLNN-UHFFFAOYSA-N 0.000 description 1
239000004808 2-ethylhexylester Substances 0.000 description 1
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235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 1
235000009849 Cucumis sativus Nutrition 0.000 description 1
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208000030852 Parasitic disease Diseases 0.000 description 1
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102100036247 Phosphatidylinositol-glycan biosynthesis class X protein Human genes 0.000 description 1
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PHYFQTYBJUILEZ-UHFFFAOYSA-N Trioleoylglycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCCCCCCCC)COC(=O)CCCCCCCC=CCCCCCCCC PHYFQTYBJUILEZ-UHFFFAOYSA-N 0.000 description 1
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125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
KFNPWTXAXKAKJU-UHFFFAOYSA-N diphenyl 2-methylidenepropanedioate Chemical compound C=1C=CC=CC=1OC(=O)C(=C)C(=O)OC1=CC=CC=C1 KFNPWTXAXKAKJU-UHFFFAOYSA-N 0.000 description 1
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125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
ODLMAHJVESYWTB-UHFFFAOYSA-N ethylmethylbenzene Natural products CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
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 description 1
239000010460 hemp oil Substances 0.000 description 1
239000002085 irritant Substances 0.000 description 1
231100000021 irritant Toxicity 0.000 description 1
231100001032 irritation of the eye Toxicity 0.000 description 1
239000000944 linseed oil Substances 0.000 description 1
235000021388 linseed oil Nutrition 0.000 description 1
208000018769 loss of vision Diseases 0.000 description 1
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239000000312 peanut oil Substances 0.000 description 1
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238000001556 precipitation Methods 0.000 description 1
239000003380 propellant Substances 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
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229960003656 ricinoleic acid Drugs 0.000 description 1
FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
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JNYAEWCLZODPBN-CTQIIAAMSA-N sorbitan Polymers OCC(O)C1OCC(O)[C@@H]1O JNYAEWCLZODPBN-CTQIIAAMSA-N 0.000 description 1
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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
- 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
- A01N25/02—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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof

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)

LU82761A 1979-09-12 1980-09-10 Compositions insecticides liquides contenant des pyrethroides synthetiques LU82761A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
IT25634/79A IT1123122B (it)	1979-09-12	1979-09-12	Composizioni liquide insetticide contenenti piretroidi sintetici
IT2563479		1979-09-12

Publications (1)

Publication Number	Publication Date
LU82761A1 true LU82761A1 (fr)	1981-04-17

Family

ID=11217315

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU82761A LU82761A1 (fr)	1979-09-12	1980-09-10	Compositions insecticides liquides contenant des pyrethroides synthetiques

Country Status (14)

Country	Link
JP (1)	JPS5655303A (da)
AU (1)	AU6214580A (da)
BE (1)	BE885221A (da)
BR (1)	BR8005817A (da)
DE (1)	DE3034039A1 (da)
DK (1)	DK381680A (da)
FR (1)	FR2464648A1 (da)
GB (1)	GB2058569A (da)
IL (1)	IL61009A0 (da)
IN (1)	IN151596B (da)
IT (1)	IT1123122B (da)
LU (1)	LU82761A1 (da)
NL (1)	NL8005055A (da)
ZA (1)	ZA805650B (da)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
HU182802B (en) *	1980-02-26	1984-03-28	Biogal Gyogyszergyar	Fotostabil delousing (insecticide) composition containing synthetic piretroides
DE3029426A1 (de) *	1980-08-02	1982-03-11	Bayer Ag, 5090 Leverkusen	Gegen zwecken wirksame pour-on-formulierungen
DE3125897A1 (de) *	1981-07-01	1983-02-10	Bayer Ag, 5090 Leverkusen	Ektoparasitizide sprueh-formulierungen
CA1211369A (en) *	1982-06-28	1986-09-16	Joseph B. Haus	Stabilized pesticidal emulsions
AU1611383A (en) *	1982-07-02	1984-01-05	Robert Young & Company Limited	Pesticidal formulation with cypermethrin
FR2533416B1 (fr) *	1982-09-29	1988-09-02	Roussel Uclaf	Nouvelles compositions pesticides renfermant un photostabilisant
FR2591227B1 (fr) *	1985-12-06	1988-11-10	Pasteur Institut	Peptides capables d'inhiber les interactions entre les virus lav et les lymphocytes t4, produits qui en sont derives et leurs applications
DE3624910A1 (de) *	1986-07-23	1988-01-28	Hoechst Ag	Konzentrierte waessrige mikroemulsionen
HU204969B (en) *	1988-04-07	1992-03-30	Chinoin Gyogyszer Es Vegyeszet	Plant protective composition against arthropoda suitable for letting out very slight quantity of agent
US5047424A (en) *	1988-10-03	1991-09-10	Safer, Inc.	Environmentally safe insecticide
HU204393B (en) *	1988-12-22	1992-01-28	Chinoin Gyogyszer Es Vegyeszet	Insecticide aqouos solutions containing piretroides as active components and microemulsion compositions containing former solutions
US5130135A (en) *	1989-08-18	1992-07-14	Smithkline Beecham Plc	Pesticidal formulations
US5591727A (en) *	1990-09-12	1997-01-07	Perycut-Chemie Ag	Insecticidal composition
MA22490A1 (fr) *	1991-04-02	1992-12-31	Rhone Poulenc Agrochimie	Composition insecticide et unite insecticide
DE4220161C2 (de) *	1992-06-19	1996-01-11	Stefes Pflanzenschutz Gmbh	Neue Formulierungen von Wirkstoffen zum Pflanzenschutz und deren Anwendung
FR2721800B1 (fr) *	1994-07-01	1997-12-26	Roussel Uclaf	Nouveaux concentres emulsionnables renfermant un u plussieurs pesticides
FR2729541B1 (fr) *	1995-01-20	2000-12-01	Jean Claude Attali	Microemulsion aqueuse insecticide et parasiticide , son procede de fabrication et d'utilisation
DE19528529A1 (de) *	1995-08-03	1997-02-06	Bayer Ag	Schädlingsbekämpfungsmittel
US5700473A (en) *	1995-08-24	1997-12-23	W. Neudorff Gmbh Kg	Triglyceride enhanced pyrethrin-based arthropodicidal composition
DE69618620D1 (de) *	1996-06-11	2002-02-21	Attavet Aubagne	Insektizide und antiparasitäre wässrige zusammensetzung, verfahren zu ihrer herstellung und verwendung
US5942542A (en) *	1996-09-29	1999-08-24	Victorian Chemical International Pty Ltd.	Insecticide adjuvants
JP3855321B2 (ja) *	1996-11-01	2006-12-06	住友化学株式会社	農薬組成物
GB0015395D0 (en) *	2000-06-26	2000-08-16	Ciba Spec Chem Water Treat Ltd	Stabilisation of light sensitive substances
RU2179805C1 (ru) *	2000-11-30	2002-02-27	Закрытое акционерное общество "Щелково Агрохим"	Масляный инсектицидный препарат на основе пиретроидов
AU2003235019A1 (en) *	2003-08-17	2005-03-03	Sirene Call Pty Ltd	Attract-and-Kill Method of Controlling Ecto-Parasites from the Order Acarina in Livestock and Domestic Animals as well as Members of the Order Artiodactyle
WO2007034275A2 (en) *	2005-09-19	2007-03-29	Battelle Uk Limited	Formulations for improved stability of pest control agents
US8153145B2 (en) *	2005-12-22	2012-04-10	Fmc Corporation	Formulations of bifenthrin and enriched cypermethrin
US20080167374A1 (en) *	2007-01-09	2008-07-10	Loveland Products, Inc.	Pesticide composition and method of use
GB201205562D0 (en) *	2012-03-29	2012-05-09	Reckitt & Colman Overseas	Liquid insecticidal compositions
ES2794124B8 (es) *	2019-05-17	2021-10-07	Grupo Agrotecnologia S L	Método y procedimiento de obtención de microbiocápsulas de piretrinas naturales con alta estabilidad

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1511646A (en) *	1974-05-08	1978-05-24	Wellcome Found	Method for insecticide use
GB1562908A (en) *	1976-12-09	1980-03-19	Ici Ltd	Insecticidal compostions
JPS53121927A (en) *	1977-03-29	1978-10-24	Sumitomo Chem Co Ltd	Insecticidal composition for electiric mosquito-repellent device
DE2862437D1 (en) *	1977-12-20	1984-09-27	Ici Plc	Insecticidal formulations and process for their preparation

1979
- 1979-09-12 IT IT25634/79A patent/IT1123122B/it active
1980
- 1980-09-08 NL NL8005055A patent/NL8005055A/nl not_active Application Discontinuation
- 1980-09-08 DK DK381680A patent/DK381680A/da not_active Application Discontinuation
- 1980-09-09 AU AU62145/80A patent/AU6214580A/en not_active Abandoned
- 1980-09-09 JP JP12413980A patent/JPS5655303A/ja active Pending
- 1980-09-09 IL IL61009A patent/IL61009A0/xx unknown
- 1980-09-10 IN IN1032/CAL/80A patent/IN151596B/en unknown
- 1980-09-10 DE DE19803034039 patent/DE3034039A1/de not_active Withdrawn
- 1980-09-10 LU LU82761A patent/LU82761A1/fr unknown
- 1980-09-10 FR FR8019511A patent/FR2464648A1/fr not_active Withdrawn
- 1980-09-11 BR BR8005817A patent/BR8005817A/pt unknown
- 1980-09-12 GB GB8029489A patent/GB2058569A/en not_active Withdrawn
- 1980-09-12 BE BE0/202094A patent/BE885221A/fr unknown
- 1980-09-12 ZA ZA00805650A patent/ZA805650B/xx unknown

Also Published As

Publication number	Publication date
BR8005817A (pt)	1981-03-24
IT1123122B (it)	1986-04-30
ZA805650B (en)	1981-09-30
BE885221A (fr)	1981-03-12
IT7925634A0 (it)	1979-09-12
DE3034039A1 (de)	1981-04-02
NL8005055A (nl)	1981-03-16
IL61009A0 (en)	1980-11-30
IN151596B (da)	1983-06-04
DK381680A (da)	1981-03-13
JPS5655303A (en)	1981-05-15
FR2464648A1 (fr)	1981-03-20
AU6214580A (en)	1981-03-19
GB2058569A (en)	1981-04-15

Publication	Publication Date	Title
LU82761A1 (fr)	1981-04-17	Compositions insecticides liquides contenant des pyrethroides synthetiques
US9596857B2 (en)	2017-03-21	Insecticidal and miticidal mixtures of bifenthrin and cyano-pyrethroids
CH693732A5 (fr)	2004-01-15	Composition parasiticide pour petits mammiferes.
KR20100134105A (ko)	2010-12-22	살충 조성물
DD211473A5 (de)	1984-07-18	Zusammensetzung zur bekaempfung von parasiten
WO1998031223A1 (fr)	1998-07-23	Composition adjuvante a usage phytosanitaire
JP2008505908A (ja)	2008-02-28	殺虫、殺ダニ、および殺真菌の組み合わせ活性を有する多機能組成物
EP0629345A1 (fr)	1994-12-21	Composition insecticide/acaricide à base d'agent(s) tensio-actif(s) anionique(s) et de substance(s) semiochimique(s), et procédé de lutte contre les arthropodes utilisant cette composition
EP0448427B1 (fr)	1995-01-11	Nouveaux esters dérivés d'acide 3-[2-cyano 2-halogéno éthényl], 2,2-diméthyl cyclopropanecarboxylique,leur procédé de préparation et leur application comme pesticides
BE1002598A6 (fr)	1991-04-09	Compositions insecticides a base de pyrethrinoides et leur utilisation.
EP0548171B1 (de)	1996-12-11	Insektizide zusammensetzung
FR2571220A1 (fr)	1986-04-11	Compositions pesticides a base de linalol et procede de lutte contre les insectes et acariens
FR2533416A1 (fr)	1984-03-30	Nouvelles compositions pesticides renfermant un photostabilisant
EP3107388B1 (fr)	2018-04-25	Composition phytosanitaire
FR2634103A1 (fr)	1990-01-19	Procede et produit permettant l'elimination des insectes nuisibles et accelerant le developpement des plantes traitees
CN117158423A (zh)	2023-12-05	一种刺吸式口器害虫趋避杀虫剂及其制备方法和应用
BE1006621A4 (fr)	1994-11-03	Procede pour combattre les insectes et produits a cet effet.
EP0007255A1 (fr)	1980-01-23	Esters d'acides cyclopropane carboxyliques substitués d'alcool alpha-cyané, leur procédé de préparation, les compositions pesticides les renfermant ainsi que leur application à titre de médicaments à usage vétérinaire
EP0521779A1 (fr)	1993-01-07	Nouveaux esters pyréthrinoides de l'alcool 4-amino 2,3,5,6-tétrafluorophényl méthylique, leur procédé de préparation et leur application comme pesticides
FR2461458A1 (fr)	1981-02-06	Pyrethrinoides a titre de regulateurs de developpement des cultures
FR2537973A1 (fr)	1984-06-22	Esters d'acides cyclopropane carboxyliques et d'alcools aliphatiques insatures, leur procede de preparation et les compositions pesticides les renfermant
FR3152945A1 (fr)	2025-03-21	Formulation à base d’huiles essentielles et son utilisation dans la lutte contre l a mouche des fruits, spécifiquement l’espèce Drosophila suzukii
EP0392928B1 (fr)	1994-07-27	Procédé de lutte contre l'Eudémis et la cochylis de la vigne, mettant en oeuvre un baculovirus de polyèdrose nucléaire
EP4723892A1 (fr)	2026-04-15	Formulation à base d'huiles essentielles et son utilisation dans la lutte contre les pucerons
FR2520197A1 (fr)	1983-07-29	Compositions insecticides et acaricides a base d'ethion et d'un pyrethroide et procede de traitement des vegetaux contre les arthropodes au moyen de ces compositions