CA1286985C - Compose pour eloigner/tuer les insectes - Google Patents

Compose pour eloigner/tuer les insectes

Info

Publication number: CA1286985C
Authority: CA; Canada
Prior art keywords: composition; percent; polymer; hydrogen; liquid carrier
Prior art date: 1986-10-10
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 - Lifetime

Application number

CA000546130A

Other languages

English (en)

Inventor

John W. Matteson

Neil A. Randen

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.)

3M Co

Original Assignee

Minnesota Mining and Manufacturing 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.)

1986-10-10

Filing date

1987-09-04

Publication date

1991-07-30

1987-09-04 Application filed by Minnesota Mining and Manufacturing Co filed Critical Minnesota Mining and Manufacturing Co

1991-07-30 Application granted granted Critical

1991-07-30 Publication of CA1286985C publication Critical patent/CA1286985C/fr

2008-07-30 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 117
231100000167 toxic agent Toxicity 0.000 title claims abstract description 17
239000003440 toxic substance Substances 0.000 title claims abstract description 17
239000000077 insect repellent Substances 0.000 title claims abstract description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 35
239000007788 liquid Substances 0.000 claims abstract description 20
239000002728 pyrethroid Substances 0.000 claims abstract description 20
241001465754 Metazoa Species 0.000 claims abstract description 16
229920000058 polyacrylate Polymers 0.000 claims abstract description 14
229920000642 polymer Polymers 0.000 claims description 32
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical group CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 23
-1 pyrethrum ester Chemical class 0.000 claims description 18
239000001257 hydrogen Substances 0.000 claims description 17
229910052739 hydrogen Inorganic materials 0.000 claims description 17
HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 claims description 17
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 13
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 13
241000238631 Hexapoda Species 0.000 claims description 13
229940070846 pyrethrins Drugs 0.000 claims description 13
239000000178 monomer Substances 0.000 claims description 11
HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 claims description 10
SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 claims description 10
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 claims description 9
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239000003963 antioxidant agent Substances 0.000 claims description 8
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
FBWNMEQMRUMQSO-UHFFFAOYSA-N tergitol NP-9 Chemical compound CCCCCCCCCC1=CC=C(OCCOCCOCCOCCOCCOCCOCCOCCOCCO)C=C1 FBWNMEQMRUMQSO-UHFFFAOYSA-N 0.000 claims description 8
DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims description 7
239000002904 solvent Substances 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 5
239000003995 emulsifying agent Substances 0.000 claims description 5
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239000006097 ultraviolet radiation absorber Substances 0.000 claims description 5
WLLGXSLBOPFWQV-UHFFFAOYSA-N MGK 264 Chemical compound C1=CC2CC1C1C2C(=O)N(CC(CC)CCCC)C1=O WLLGXSLBOPFWQV-UHFFFAOYSA-N 0.000 claims description 4
240000004460 Tanacetum coccineum Species 0.000 claims description 4
239000002253 acid Substances 0.000 claims description 4
125000005907 alkyl ester group Chemical group 0.000 claims description 4
230000003078 antioxidant effect Effects 0.000 claims description 4
150000002431 hydrogen Chemical group 0.000 claims description 4
238000000034 method Methods 0.000 claims description 4
229920001897 terpolymer Polymers 0.000 claims description 4
239000002917 insecticide Substances 0.000 claims description 3
DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 claims description 3
238000006116 polymerization reaction Methods 0.000 claims description 3
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UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
239000012965 benzophenone Substances 0.000 claims description 2
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LJWQETZTWPNCDZ-UHFFFAOYSA-N 1-(2-hydroxyethoxy)-2-[(6-propyl-1,3-benzodioxol-5-yl)methyl]hexan-2-ol Chemical compound C1=C(CCC)C(CC(O)(COCCO)CCCC)=CC2=C1OCO2 LJWQETZTWPNCDZ-UHFFFAOYSA-N 0.000 claims 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
230000001846 repelling effect Effects 0.000 claims 1
238000009472 formulation Methods 0.000 description 51
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 17
FMRHJJZUHUTGKE-UHFFFAOYSA-N Ethylhexyl salicylate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1O FMRHJJZUHUTGKE-UHFFFAOYSA-N 0.000 description 15
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 14
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 12
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 description 11
239000004615 ingredient Substances 0.000 description 9
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238000004166 bioassay Methods 0.000 description 7
239000003350 kerosene Substances 0.000 description 7
239000003921 oil Substances 0.000 description 7
241000255925 Diptera Species 0.000 description 6
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235000019439 ethyl acetate Nutrition 0.000 description 6
239000000284 extract Substances 0.000 description 6
241000283690 Bos taurus Species 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 5
239000000969 carrier Substances 0.000 description 5
WLLGXSLBOPFWQV-OTHKPKEBSA-N molport-035-783-878 Chemical compound C([C@H]1C=C2)[C@H]2C2C1C(=O)N(CC(CC)CCCC)C2=O WLLGXSLBOPFWQV-OTHKPKEBSA-N 0.000 description 5
VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound 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 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 5
ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 4
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 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 class 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
239000006096 absorbing agent Substances 0.000 description 4
CMDKPGRTAQVGFQ-RMKNXTFCSA-N cinoxate Chemical compound CCOCCOC(=O)\C=C\C1=CC=C(OC)C=C1 CMDKPGRTAQVGFQ-RMKNXTFCSA-N 0.000 description 4
230000000694 effects Effects 0.000 description 4
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125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
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WYWZRNAHINYAEF-UHFFFAOYSA-N Padimate O Chemical compound CCCCC(CC)COC(=O)C1=CC=C(N(C)C)C=C1 WYWZRNAHINYAEF-UHFFFAOYSA-N 0.000 description 3
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MEZZCSHVIGVWFI-UHFFFAOYSA-N 2,2'-Dihydroxy-4-methoxybenzophenone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1O MEZZCSHVIGVWFI-UHFFFAOYSA-N 0.000 description 2
WHQOKFZWSDOTQP-UHFFFAOYSA-N 2,3-dihydroxypropyl 4-aminobenzoate Chemical compound NC1=CC=C(C(=O)OCC(O)CO)C=C1 WHQOKFZWSDOTQP-UHFFFAOYSA-N 0.000 description 2
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125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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150000002500 ions Chemical class 0.000 description 1
WKNSDDMJXANVMK-XIGJTORUSA-N jasmolin II Chemical compound C1C(=O)C(C\C=C/CC)=C(C)[C@H]1OC(=O)[C@H]1C(C)(C)[C@@H]1\C=C(/C)C(=O)OC WKNSDDMJXANVMK-XIGJTORUSA-N 0.000 description 1
WKNSDDMJXANVMK-UHFFFAOYSA-N jasmolin II Natural products C1C(=O)C(CC=CCC)=C(C)C1OC(=O)C1C(C)(C)C1C=C(C)C(=O)OC WKNSDDMJXANVMK-UHFFFAOYSA-N 0.000 description 1
239000012669 liquid formulation Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
230000003020 moisturizing effect Effects 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Chemical compound CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
239000007764 o/w emulsion Substances 0.000 description 1
QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 1
229960001679 octinoxate Drugs 0.000 description 1
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
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 description 1
229960000490 permethrin Drugs 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229960000969 phenyl salicylate Drugs 0.000 description 1
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
ROVGZAWFACYCSP-VUMXUWRFSA-N pyrethrin I Chemical compound 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 ROVGZAWFACYCSP-VUMXUWRFSA-N 0.000 description 1
229940108410 resmethrin Drugs 0.000 description 1
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 description 1
150000003902 salicylic acid esters Chemical class 0.000 description 1
ZQBAKBUEJOMQEX-UHFFFAOYSA-N salicylic acid phenyl ester Natural products OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
230000035900 sweating Effects 0.000 description 1
LVEOKSIILWWVEO-UHFFFAOYSA-N tetradecyl 3-(3-oxo-3-tetradecoxypropyl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCC LVEOKSIILWWVEO-UHFFFAOYSA-N 0.000 description 1
229960005199 tetramethrin Drugs 0.000 description 1
150000007970 thio esters Chemical class 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 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
- 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
- A01N25/24—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 to enhance the sticking of the active ingredients

Landscapes

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

CA000546130A 1986-10-10 1987-09-04 Compose pour eloigner/tuer les insectes Expired - Lifetime CA1286985C (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US91747886A	1986-10-10	1986-10-10
US917,478		1986-10-10

Publications (1)

Publication Number	Publication Date
CA1286985C true CA1286985C (fr)	1991-07-30

Family

ID=25438847

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000546130A Expired - Lifetime CA1286985C (fr)	1986-10-10	1987-09-04	Compose pour eloigner/tuer les insectes

Country Status (3)

Country	Link
AU (1)	AU603376B2 (fr)
CA (1)	CA1286985C (fr)
NZ (1)	NZ221641A (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1995017814A1 (fr) *	1993-12-30	1995-07-06	Minnesota Mining And Manufacturing Company	Batonnet de lutte contre les ectoparasites pour animaux domestiques
WO2019038760A1 (fr) *	2017-08-20	2019-02-28	Adhestick Innovations Ltd.	Formulations durables de répulsion de nuisibles

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP3594963B2 (ja)	1992-09-25	2004-12-02	ミネソタマイニングアンドマニュファクチャリングカンパニー	粘着力増強特性をもつ皮ふ処理の方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ZA859160B (en) *	1984-08-29	1986-07-30	Denis Glynn Catton	Dip compositions
US4808615A (en) *	1985-04-19	1989-02-28	Carter-Wallace, Inc.	Flea and tick infestation control composition containing chlorpyrifos and vinyl acetate/crotonic acid/vinyl neodecanoate copolymer
WO1987002580A1 (fr) *	1985-11-04	1987-05-07	Dermatological Products Of Texas	Vehicules pharmaceutiques filmogenes pour l'application de medicaments sur les ongles, compositions pharmaceutiques a base de ces vehicules, et leurs procedes d'utilisation

1987
- 1987-09-02 NZ NZ22164187A patent/NZ221641A/xx unknown
- 1987-09-04 CA CA000546130A patent/CA1286985C/fr not_active Expired - Lifetime
- 1987-09-08 AU AU78142/87A patent/AU603376B2/en not_active Ceased

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1995017814A1 (fr) *	1993-12-30	1995-07-06	Minnesota Mining And Manufacturing Company	Batonnet de lutte contre les ectoparasites pour animaux domestiques
WO2019038760A1 (fr) *	2017-08-20	2019-02-28	Adhestick Innovations Ltd.	Formulations durables de répulsion de nuisibles
EP3668315A4 (fr) *	2017-08-20	2022-01-26	Adhestick Innovations Ltd.	Formulations durables de répulsion de nuisibles
US11696582B2 (en)	2017-08-20	2023-07-11	Adhestick Innovations Ltd.	Durable pest-repelling formulations

Also Published As

Publication number	Publication date
NZ221641A (en)	1990-05-28
AU7814287A (en)	1988-04-14
AU603376B2 (en)	1990-11-15

Legal Events

Date	Code	Title	Description
1995-01-31	MKLA	Lapsed

Publication	Publication Date	Title
PL174547B1 (pl)	1998-08-31	Pestycyd do zwalczania insektów
DE9012996U1 (de)	1991-10-10	Insektizides Produkt
WO2013165477A1 (fr)	2013-11-07	Lutte contre les moustiques et répulsion des moustiques
JPS5459269A (en)	1979-05-12	Carboxylic esters, their preparation and insecticide and acaricide containing the same as effective component.
PL188073B1 (pl)	2004-12-31	Kompozycja szkodnikobójcza, sposób wytwarzania kompozycji szkodnikobójczej i jej zastosowanie
US5854284A (en)	1998-12-29	Candle for dispersion of insect repellent based on DEET
KR20010058310A (ko)	2001-07-05	방충 조성물 및 이를 사용한 방충 도료
ES2230600T3 (es)	2005-05-01	Metodos de utilizacion de aceite de emu y fracciones activas del mismo como repelente de insectos.
CA2311421C (fr)	2004-06-15	Insectifuge
DE69907538T2 (de)	2004-02-19	Gewebeschutzmittel gegen Schädlinge
CA1250229A (fr)	1989-02-21	Pesticide
CA2091064C (fr)	2000-06-27	Composition insecticide
CA1286985C (fr)	1991-07-30	Compose pour eloigner/tuer les insectes
KR20060073726A (ko)	2006-06-29	페닐 에틸 알콜을 이용한 모기 기피제 조성물
CA2068039A1 (fr)	1993-06-28	Repulsif utile contre les ixodes
US5591727A (en)	1997-01-07	Insecticidal composition
EP0888716B1 (fr)	2003-03-12	Agent répulsif à l'égard des moustiques et méthodes pour repousser les moustiques
CN114206111A (zh)	2022-03-18	节肢动物驱避组合物
WO2008143376A1 (fr)	2008-11-27	Répulsif anti-moustiques
RU2107437C1 (ru)	1998-03-27	Аттрактант для мух и способ привлечения мух
KR20110064606A (ko)	2011-06-15	파네센 또는 야래향 꽃 향취 성분을 포함하는 모기 퇴치제 조성물
KR100445171B1 (ko)	2004-08-21	방충 마이크로 캡슐을 함유한 섬유유연제 조성물
CA2111909A1 (fr)	1994-06-22	Composition repulsive
JPS56156238A (en)	1981-12-02	Carboxylic acid ester, its preparation and insecticidal and acaricidal agent containing the same as active component
AU782551B2 (en)	2005-08-11	Pest repellent