LT3606B - Insecticidal composition - Google Patents

Insecticidal composition Download PDF

Info

Publication number: LT3606B
Authority: LT; Lithuania
Prior art keywords: insecticidal composition; carboxylic acid; parts; acid ester; compound
Prior art date: 1990-04-24

Application number

LTIP1063A

Other languages

English (en)

Lithuanian (lt)

Inventor

Kazunobu Dohara

Mitsuyasu Makita

Yasuo Abe

Original Assignee

Sumitomo 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.)

1990-04-24

Filing date

1993-09-21

Publication date

1995-12-27

1990-04-24 Priority claimed from JP2109840A external-priority patent/JPH0764687B2/ja

1993-09-21 Application filed by Sumitomo Chemical Co filed Critical Sumitomo Chemical Co

1995-04-25 Publication of LTIP1063A publication Critical patent/LTIP1063A/xx

1995-12-27 Publication of LT3606B publication Critical patent/LT3606B/lt

Links

230000000749 insecticidal effect Effects 0.000 title claims abstract description 23
239000000203 mixture Substances 0.000 title claims description 37
-1 2,4-dioxo-1-(2-propynyl) imidazolidine-3-ylmethyl Chemical group 0.000 claims abstract description 14
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims abstract description 10
HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 claims abstract description 8
XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 claims abstract description 4
CMBYOWLFQAFZCP-UHFFFAOYSA-N Hexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCCC CMBYOWLFQAFZCP-UHFFFAOYSA-N 0.000 claims abstract 2
229940100463 hexyl laurate Drugs 0.000 claims abstract 2
125000004432 carbon atom Chemical group C* 0.000 claims description 8
150000001733 carboxylic acid esters Chemical class 0.000 claims description 8
150000001990 dicarboxylic acid derivatives Chemical class 0.000 claims description 4
229940126062 Compound A Drugs 0.000 description 14
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 14
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
239000003380 propellant Substances 0.000 description 9
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 8
XLOPRKKSAJMMEW-SFYZADRCSA-M (R,R)-chrysanthemate Chemical compound CC(C)=C[C@@H]1[C@@H](C([O-])=O)C1(C)C XLOPRKKSAJMMEW-SFYZADRCSA-M 0.000 description 7
150000001875 compounds Chemical class 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
241000255925 Diptera Species 0.000 description 4
241000257159 Musca domestica Species 0.000 description 4
239000001273 butane Substances 0.000 description 4
239000003350 kerosene Substances 0.000 description 4
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 4
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
230000000052 comparative effect Effects 0.000 description 3
239000002917 insecticide Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
LLMLSUSAKZVFOA-UJURSFKZSA-N (1S,3R)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@@H]1C(O)=O LLMLSUSAKZVFOA-UJURSFKZSA-N 0.000 description 2
LNJXZKBHJZAIKQ-UHFFFAOYSA-N 1,1,1,2-tetrachloro-3-(2,3,3,3-tetrachloropropoxy)propane Chemical compound ClC(Cl)(Cl)C(Cl)COCC(Cl)C(Cl)(Cl)Cl LNJXZKBHJZAIKQ-UHFFFAOYSA-N 0.000 description 2
NFGXHKASABOEEW-UHFFFAOYSA-N 1-methylethyl 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate Chemical compound COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C NFGXHKASABOEEW-UHFFFAOYSA-N 0.000 description 2
241000238876 Acari Species 0.000 description 2
241000238662 Blatta orientalis Species 0.000 description 2
241000238657 Blattella germanica Species 0.000 description 2
241001674044 Blattodea Species 0.000 description 2
241000238631 Hexapoda Species 0.000 description 2
241000256602 Isoptera Species 0.000 description 2
241000238675 Periplaneta americana Species 0.000 description 2
241001510001 Periplaneta brunnea Species 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
239000000443 aerosol Substances 0.000 description 2
239000000969 carrier Substances 0.000 description 2
LVQDKIWDGQRHTE-UHFFFAOYSA-N cyromazine Chemical compound NC1=NC(N)=NC(NC2CC2)=N1 LVQDKIWDGQRHTE-UHFFFAOYSA-N 0.000 description 2
KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 2
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 description 2
239000006260 foam Substances 0.000 description 2
238000009472 formulation Methods 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
239000007787 solid Substances 0.000 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 description 1
FJDPATXIBIBRIM-QFMSAKRMSA-N (1R)-trans-cyphenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 FJDPATXIBIBRIM-QFMSAKRMSA-N 0.000 description 1
KYCXOPFICRVUPB-UHFFFAOYSA-N (2-propan-2-yloxyphenyl)methyl carbamate Chemical compound CC(C)OC1=CC=CC=C1COC(N)=O KYCXOPFICRVUPB-UHFFFAOYSA-N 0.000 description 1
OHAMOQALFCXZBV-UHFFFAOYSA-N 2,2-dichloroethenyl 2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)CC1C(=O)OC=C(Cl)Cl OHAMOQALFCXZBV-UHFFFAOYSA-N 0.000 description 1
241000132121 Acaridae Species 0.000 description 1
241000256111 Aedes <genus> Species 0.000 description 1
241000256118 Aedes aegypti Species 0.000 description 1
241000256173 Aedes albopictus Species 0.000 description 1
241000256186 Anopheles <genus> Species 0.000 description 1
241001279740 Anopheles sinensis Species 0.000 description 1
241001414896 Anthomyiidae Species 0.000 description 1
241000239290 Araneae Species 0.000 description 1
241001503477 Athalia rosae Species 0.000 description 1
241001124657 Bethylidae Species 0.000 description 1
241000257161 Calliphoridae Species 0.000 description 1
241001177891 Cheyletidae Species 0.000 description 1
241000255930 Chironomidae Species 0.000 description 1
241001509962 Coptotermes formosanus Species 0.000 description 1
241000256054 Culex <genus> Species 0.000 description 1
241000144210 Culex pipiens pallens Species 0.000 description 1
239000005946 Cypermethrin Substances 0.000 description 1
239000005891 Cyromazine Substances 0.000 description 1
241001414890 Delia Species 0.000 description 1
241000084475 Delia antiqua Species 0.000 description 1
241001609607 Delia platura Species 0.000 description 1
239000005892 Deltamethrin Substances 0.000 description 1
241000238713 Dermatophagoides farinae Species 0.000 description 1
241000709823 Dictyoptera <beetle genus> Species 0.000 description 1
239000005893 Diflubenzuron Substances 0.000 description 1
241000255581 Drosophila <fruit fly, genus> Species 0.000 description 1
241000953886 Fannia canicularis Species 0.000 description 1
241001507629 Formicidae Species 0.000 description 1
FSYXMFXBRJFYBS-UHFFFAOYSA-N Furamethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=CC=C(CC#C)O1 FSYXMFXBRJFYBS-UHFFFAOYSA-N 0.000 description 1
241000257303 Hymenoptera Species 0.000 description 1
241000238889 Ixodidae Species 0.000 description 1
241000255777 Lepidoptera Species 0.000 description 1
WLLGXSLBOPFWQV-UHFFFAOYSA-N MGK 264 Chemical compound C1=CC2CC1C1C2C(=O)N(CC(CC)CCCC)C1=O WLLGXSLBOPFWQV-UHFFFAOYSA-N 0.000 description 1
241000581981 Muscina stabulans Species 0.000 description 1
241001510010 Periplaneta fuliginosa Species 0.000 description 1
241001674048 Phthiraptera Species 0.000 description 1
241000255131 Psychodidae Species 0.000 description 1
241000866500 Reticulitermes speratus Species 0.000 description 1
ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 1
241000190070 Sarracenia purpurea Species 0.000 description 1
241000256103 Simuliidae Species 0.000 description 1
241000255628 Tabanidae Species 0.000 description 1
241001124685 Tenthredinidae Species 0.000 description 1
241000255588 Tephritidae Species 0.000 description 1
241000130771 Tinea pellionella Species 0.000 description 1
241000611866 Tyrophagus putrescentiae Species 0.000 description 1
241000256856 Vespidae Species 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
HOWJQLVNDUGZBI-UHFFFAOYSA-N butane;propane Chemical compound CCC.CCCC HOWJQLVNDUGZBI-UHFFFAOYSA-N 0.000 description 1
235000014633 carbohydrates Nutrition 0.000 description 1
229960001591 cyfluthrin Drugs 0.000 description 1
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 description 1
229960005424 cypermethrin Drugs 0.000 description 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 description 1
229950000775 cyromazine Drugs 0.000 description 1
229960002483 decamethrin Drugs 0.000 description 1
230000002950 deficient Effects 0.000 description 1
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 description 1
OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 1
QQQYTWIFVNKMRW-UHFFFAOYSA-N diflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(Cl)C=C1 QQQYTWIFVNKMRW-UHFFFAOYSA-N 0.000 description 1
229940019503 diflubenzuron Drugs 0.000 description 1
230000000694 effects Effects 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
239000000796 flavoring agent Substances 0.000 description 1
235000013355 food flavoring agent Nutrition 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229950003442 methoprene Drugs 0.000 description 1
229930002897 methoprene Natural products 0.000 description 1
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 1
230000003287 optical effect Effects 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
229960000490 permethrin Drugs 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
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
125000003386 piperidinyl group Chemical group 0.000 description 1
SMKRKQBMYOFFMU-UHFFFAOYSA-N prallethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OC1C(C)=C(CC#C)C(=O)C1 SMKRKQBMYOFFMU-UHFFFAOYSA-N 0.000 description 1
239000001294 propane Substances 0.000 description 1
125000004805 propylene group Chemical class [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-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
230000035939 shock Effects 0.000 description 1
229960005199 tetramethrin Drugs 0.000 description 1
210000002700 urine Anatomy 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles

Landscapes

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

LTIP1063A 1990-04-24 1993-09-21 Insecticidal composition LT3606B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP2109840A JPH0764687B2 (ja)	1990-04-24	1990-04-24	殺虫組成物

Publications (2)

Publication Number	Publication Date
LTIP1063A LTIP1063A (en)	1995-04-25
LT3606B true LT3606B (en)	1995-12-27

Family

ID=14520536

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LTIP1063A LT3606B (en)	1990-04-24	1993-09-21	Insecticidal composition

Country Status (11)

Country	Link
KR (1)	KR0161534B1 (fr)
BR (1)	BR9101639A (fr)
CA (1)	CA2040370C (fr)
ES (1)	ES2035768B1 (fr)
LT (1)	LT3606B (fr)
LV (1)	LV10158B (fr)
MX (1)	MX172672B (fr)
PT (1)	PT97450B (fr)
RU (1)	RU2035142C1 (fr)
YU (1)	YU47780B (fr)
ZA (1)	ZA912907B (fr)

Families Citing this family (3)

* 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
JP3855311B2 (ja) *	1996-08-07	2006-12-06	住友化学株式会社	エアゾール組成物
RU2153256C1 (ru) *	1999-03-16	2000-07-27	Всероссийский научно-исследовательский институт масличных культур им. В.С. Пустовойта	Инсектицидное средство и способ борьбы с вредителями сельскохозяйственных культур

Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4176189A (en)	1977-06-20	1979-11-27	Sumitomo Chemical Company, Limited	Insecticidal and acaricidal hydantoin N-methylol esters

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5147774B2 (fr) *	1972-04-05	1976-12-16
JPS5372821A (en) *	1976-12-09	1978-06-28	Sumitomo Chem Co Ltd	Aerosol insecticides
IT1114770B (it) *	1977-03-23	1986-01-27	Bernabe Giuseppina	Composizione per la regolare e prolungata volatilizzazione di un insetticida piretrinico
JPS5428818A (en) *	1977-08-05	1979-03-03	Fumakilla Ltd	Method of enhancing effect of pesticide smoked in short time
DE3029426A1 (de) *	1980-08-02	1982-03-11	Bayer Ag, 5090 Leverkusen	Gegen zwecken wirksame pour-on-formulierungen
DE3317823A1 (de) *	1983-05-17	1984-11-22	Bayer Ag, 5090 Leverkusen	Schaedlingsbekaempfungsmittel
JPS60139605A (ja) *	1983-12-27	1985-07-24	Sumitomo Chem Co Ltd	燻蒸組成物
AU611590B2 (en) *	1988-11-11	1991-06-13	Sumitomo Chemical Company, Limited	Insecticidal composition comprising 2,4-dioxo-1-(2- propynyl)imidazolidin-3-ylmethyl chrysanthemate, organic solvent and kerosine, and an aerosol containing same

1991
- 1991-04-12 CA CA002040370A patent/CA2040370C/fr not_active Expired - Lifetime
- 1991-04-18 ZA ZA912907A patent/ZA912907B/xx unknown
- 1991-04-23 MX MX025480A patent/MX172672B/es unknown
- 1991-04-23 PT PT97450A patent/PT97450B/pt not_active IP Right Cessation
- 1991-04-23 BR BR919101639A patent/BR9101639A/pt not_active Application Discontinuation
- 1991-04-23 YU YU73691A patent/YU47780B/sh unknown
- 1991-04-23 ES ES9101021A patent/ES2035768B1/es not_active Expired - Fee Related
- 1991-04-23 RU SU914895311A patent/RU2035142C1/ru active
- 1991-04-24 KR KR1019910006610A patent/KR0161534B1/ko not_active Expired - Lifetime
1992
- 1992-12-22 LV LVP-92-387A patent/LV10158B/lv unknown
1993
- 1993-09-21 LT LTIP1063A patent/LT3606B/lt not_active IP Right Cessation

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4176189A (en)	1977-06-20	1979-11-27	Sumitomo Chemical Company, Limited	Insecticidal and acaricidal hydantoin N-methylol esters

Also Published As

Publication number	Publication date
YU47780B (sr)	1996-01-09
LV10158B (en)	1995-06-20
ZA912907B (en)	1992-12-30
RU2035142C1 (ru)	1995-05-20
PT97450A (pt)	1992-01-31
LTIP1063A (en)	1995-04-25
ES2035768B1 (es)	1994-02-01
KR910017934A (ko)	1991-11-30
YU73691A (sh)	1994-01-20
BR9101639A (pt)	1991-12-10
LV10158A (lv)	1994-10-20
CA2040370C (fr)	2000-11-14
PT97450B (pt)	1998-08-31
MX172672B (es)	1994-01-06
ES2035768A1 (es)	1993-04-16
CA2040370A1 (fr)	1991-10-25
KR0161534B1 (ko)	1998-11-16

Legal Events

Date	Code	Title	Description
1999-05-25	MM9A	Lapsed patents	Effective date: 19980921

Publication	Publication Date	Title
RU2455825C2 (ru)	2012-07-20	Пестицидная аэрозольная композиция
ZA200100754B (en)	2002-01-28	Synergistic and residual pesticidal compositions containing plant essential oils.
US4940729A (en)	1990-07-10	Pesticidal formulations
US5190745A (en)	1993-03-02	Insecticidal compositions
TWI641319B (zh)	2018-11-21	用以防治室內害蟲的氣溶膠
US8114897B2 (en)	2012-02-14	Pesticidal composition and method for controlling a pest
US5872143A (en)	1999-02-16	Insecticidal aerosol composition and insecticidal composition for preparation of same
AU636471B2 (en)	1993-04-29	Insecticidal compositions
CN1233237C (zh)	2005-12-28	杀虫喷雾剂组成及杀虫方法
AU627792B2 (en)	1992-09-03	Method for controlling insects and/or acarines
JP3008603B2 (ja)	2000-02-14	殺虫組成物
LT3606B (en)	1995-12-27	Insecticidal composition
Barlow et al.	1975	The insecticidal activity of some synthetic pyrethroids against mosquitoes and flies
JP2855724B2 (ja)	1999-02-10	エアゾール殺虫剤
HU193027B (en)	1987-08-28	Insecticide compositions containing pyrethroid derivatives as active substances
FR2781984A1 (fr)	2000-02-11	Composition pesticide et procede de lutte contre les nuisibles l'utilisant
SI9110736A (sl)	1997-12-31	Insekticidne sestave
JP2000080006A (ja)	2000-03-21	殺虫エアゾール組成物
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