CA1054049A - Insecticide liquide concentre - Google Patents

Insecticide liquide concentre

Info

Publication number: CA1054049A
Authority: CA; Canada
Prior art keywords: composition; organo; concentrate; phosphorus compound; aqueous
Prior art date: 1976-11-17
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

Application number

CA265,888A

Other languages

English (en)

Inventor

Hiroshi Watanabe

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.)

Osaka Kasei Co Ltd

Nippon Kayaku Co Ltd

Original Assignee

Osaka Kasei Co Ltd

Nippon Kayaku Co Ltd

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.)

1976-11-17

Filing date

1976-11-17

Publication date

1979-05-08

1976-11-17 Application filed by Osaka Kasei Co Ltd, Nippon Kayaku Co Ltd filed Critical Osaka Kasei Co Ltd

1976-11-17 Priority to CA265,888A priority Critical patent/CA1054049A/fr

1979-05-08 Application granted granted Critical

1979-05-08 Publication of CA1054049A publication Critical patent/CA1054049A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 80
239000012141 concentrate Substances 0.000 title claims abstract description 73
230000000749 insecticidal effect Effects 0.000 title claims abstract description 58
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 32
150000002903 organophosphorus compounds Chemical class 0.000 claims abstract description 27
239000004094 surface-active agent Substances 0.000 claims abstract description 15
-1 methylthio, 2-isopropyl-4-methyl-6-pyrimidinyl Chemical group 0.000 claims description 21
150000001875 compounds Chemical class 0.000 claims description 16
239000003960 organic solvent Substances 0.000 claims description 15
239000003381 stabilizer Substances 0.000 claims description 9
RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 claims description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
229940121375 antifungal agent Drugs 0.000 claims description 4
239000003429 antifungal agent Substances 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
239000003495 polar organic solvent Substances 0.000 claims description 4
239000004593 Epoxy Substances 0.000 claims description 3
239000004288 Sodium dehydroacetate Substances 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
229910052760 oxygen Inorganic materials 0.000 claims description 2
239000001301 oxygen Substances 0.000 claims description 2
229940079839 sodium dehydroacetate Drugs 0.000 claims description 2
235000019259 sodium dehydroacetate Nutrition 0.000 claims description 2
DSOWAKKSGYUMTF-GZOLSCHFSA-M sodium;(1e)-1-(6-methyl-2,4-dioxopyran-3-ylidene)ethanolate Chemical group [Na+].C\C([O-])=C1/C(=O)OC(C)=CC1=O DSOWAKKSGYUMTF-GZOLSCHFSA-M 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
229910052717 sulfur Inorganic materials 0.000 claims description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
VRAKDAYLTPMBAW-UHFFFAOYSA-N [O-][N+](=O)ClC#N Chemical group [O-][N+](=O)ClC#N VRAKDAYLTPMBAW-UHFFFAOYSA-N 0.000 claims 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
239000011593 sulfur Substances 0.000 claims 1
235000008504 concentrate Nutrition 0.000 description 68
239000000243 solution Substances 0.000 description 27
238000012360 testing method Methods 0.000 description 21
FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 18
239000002917 insecticide Substances 0.000 description 18
PNVJTZOFSHSLTO-UHFFFAOYSA-N Fenthion Chemical compound COP(=S)(OC)OC1=CC=C(SC)C(C)=C1 PNVJTZOFSHSLTO-UHFFFAOYSA-N 0.000 description 17
238000000034 method Methods 0.000 description 17
239000004495 emulsifiable concentrate Substances 0.000 description 14
229910052698 phosphorus Inorganic materials 0.000 description 10
239000011574 phosphorus Substances 0.000 description 10
231100000419 toxicity Toxicity 0.000 description 9
230000001988 toxicity Effects 0.000 description 9
241000251468 Actinopterygii Species 0.000 description 8
241000700159 Rattus Species 0.000 description 8
239000011521 glass Substances 0.000 description 8
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 7
239000005977 Ethylene Substances 0.000 description 7
JHJOOSLFWRRSGU-UHFFFAOYSA-N Fenchlorphos Chemical compound COP(=S)(OC)OC1=CC(Cl)=C(Cl)C=C1Cl JHJOOSLFWRRSGU-UHFFFAOYSA-N 0.000 description 7
241000699670 Mus sp. Species 0.000 description 7
238000003756 stirring Methods 0.000 description 7
241000255925 Diptera Species 0.000 description 6
241000238631 Hexapoda Species 0.000 description 6
239000007864 aqueous solution Substances 0.000 description 6
BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 6
229910000402 monopotassium phosphate Inorganic materials 0.000 description 6
235000019796 monopotassium phosphate Nutrition 0.000 description 6
PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 description 6
241001465754 Metazoa Species 0.000 description 5
241000257226 Muscidae Species 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
238000010998 test method Methods 0.000 description 5
241000276423 Fundulus heteroclitus Species 0.000 description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
239000007853 buffer solution Substances 0.000 description 4
238000000354 decomposition reaction Methods 0.000 description 4
238000007654 immersion Methods 0.000 description 4
230000007794 irritation Effects 0.000 description 4
238000002156 mixing Methods 0.000 description 4
230000001473 noxious effect Effects 0.000 description 4
239000011734 sodium Substances 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
AOBIOSPNXBMOAT-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane Chemical compound C1OC1COCCOCC1CO1 AOBIOSPNXBMOAT-UHFFFAOYSA-N 0.000 description 3
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical class ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
239000002202 Polyethylene glycol Substances 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 3
239000003002 pH adjusting agent Substances 0.000 description 3
230000000361 pesticidal effect Effects 0.000 description 3
239000011120 plywood Substances 0.000 description 3
229920001223 polyethylene glycol Polymers 0.000 description 3
239000002904 solvent Substances 0.000 description 3
RNMDNPCBIKJCQP-UHFFFAOYSA-N 5-nonyl-7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-ol Chemical compound C(CCCCCCCC)C1=C2C(=C(C=C1)O)O2 RNMDNPCBIKJCQP-UHFFFAOYSA-N 0.000 description 2
241001674044 Blattodea Species 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
239000005949 Malathion Substances 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
241000283973 Oryctolagus cuniculus Species 0.000 description 2
230000001154 acute effect Effects 0.000 description 2
230000007059 acute toxicity Effects 0.000 description 2
231100000403 acute toxicity Toxicity 0.000 description 2
229910021538 borax Inorganic materials 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
231100000636 lethal dose Toxicity 0.000 description 2
229960000453 malathion Drugs 0.000 description 2
239000000463 material Substances 0.000 description 2
125000000962 organic group Chemical group 0.000 description 2
150000003018 phosphorus compounds Chemical class 0.000 description 2
230000002265 prevention Effects 0.000 description 2
239000000523 sample Substances 0.000 description 2
239000004328 sodium tetraborate Substances 0.000 description 2
235000010339 sodium tetraborate Nutrition 0.000 description 2
238000005507 spraying Methods 0.000 description 2
231100000331 toxic Toxicity 0.000 description 2
230000002588 toxic effect Effects 0.000 description 2
JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 description 1
LHXNVCCLDTYJGT-UHFFFAOYSA-N 1-(oxiran-2-ylmethoxy)propan-2-ol Chemical compound CC(O)COCC1CO1 LHXNVCCLDTYJGT-UHFFFAOYSA-N 0.000 description 1
IVIDDMGBRCPGLJ-UHFFFAOYSA-N 2,3-bis(oxiran-2-ylmethoxy)propan-1-ol Chemical compound C1OC1COC(CO)COCC1CO1 IVIDDMGBRCPGLJ-UHFFFAOYSA-N 0.000 description 1
CUGZWHZWSVUSBE-UHFFFAOYSA-N 2-(oxiran-2-ylmethoxy)ethanol Chemical compound OCCOCC1CO1 CUGZWHZWSVUSBE-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
241000238657 Blattella germanica Species 0.000 description 1
241000252229 Carassius auratus Species 0.000 description 1
241000256135 Chironomus thummi Species 0.000 description 1
241000518994 Conta Species 0.000 description 1
241000256054 Culex <genus> Species 0.000 description 1
VVNCNSJFMMFHPL-VKHMYHEASA-N D-penicillamine Chemical compound CC(C)(S)[C@@H](N)C(O)=O VVNCNSJFMMFHPL-VKHMYHEASA-N 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
206010061218 Inflammation Diseases 0.000 description 1
239000006169 McIlvaine's buffer solution Substances 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
241000699666 Mus <mouse, genus> Species 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
206010030113 Oedema Diseases 0.000 description 1
241000238814 Orthoptera Species 0.000 description 1
FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical group C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
206010039509 Scab Diseases 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
101100162169 Xenopus laevis adrm1-a gene Proteins 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000013543 active substance Substances 0.000 description 1
238000003915 air pollution Methods 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
238000004040 coloring Methods 0.000 description 1
239000006071 cream Substances 0.000 description 1
229940075911 depen Drugs 0.000 description 1
230000002951 depilatory effect Effects 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-M dihydrogenphosphate Chemical compound OP(O)([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-M 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
125000004119 disulfanediyl group Chemical group *SS* 0.000 description 1
GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
230000004054 inflammatory process Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
231100000037 inhalation toxicity test Toxicity 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
231100000518 lethal Toxicity 0.000 description 1
230000001665 lethal effect Effects 0.000 description 1
210000004373 mandible Anatomy 0.000 description 1
239000012528 membrane Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229940063559 methacrylic acid Drugs 0.000 description 1
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
238000010979 pH adjustment Methods 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
239000003542 rubefacient Substances 0.000 description 1
239000012488 sample solution Substances 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
210000002784 stomach Anatomy 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
239000002352 surface water Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
231100000820 toxicity test Toxicity 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
238000003911 water pollution Methods 0.000 description 1
235000020681 well water Nutrition 0.000 description 1
239000002349 well water Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)

CA265,888A 1976-11-17 1976-11-17 Insecticide liquide concentre Expired CA1054049A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA265,888A CA1054049A (fr)	1976-11-17	1976-11-17	Insecticide liquide concentre

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA265,888A CA1054049A (fr)	1976-11-17	1976-11-17	Insecticide liquide concentre

Publications (1)

Publication Number	Publication Date
CA1054049A true CA1054049A (fr)	1979-05-08

Family

ID=4107305

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA265,888A Expired CA1054049A (fr)	1976-11-17	1976-11-17	Insecticide liquide concentre

Country Status (1)

Country	Link
CA (1)	CA1054049A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4388297A (en)	1980-06-19	1983-06-14	The Dow Chemical Company	Stable tocicant compositions of chlorpyrifos

1976
- 1976-11-17 CA CA265,888A patent/CA1054049A/fr not_active Expired

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4388297A (en)	1980-06-19	1983-06-14	The Dow Chemical Company	Stable tocicant compositions of chlorpyrifos

Publication	Publication Date	Title
JP2525632B2 (ja)	1996-08-21	シロアリの駆除方法
US4536506A (en)	1985-08-20	Insecticidal and acaricidal combination containing a pyrethroid
NO176175B (no)	1994-11-07	Preparat for bruk innen agrikultur
JPH07507307A (ja)	1995-08-10	ヘキサフルムロンおよび関連化合物の殺白蟻剤としての新規な使用
BG65394B1 (bg)	2008-06-30	Хербицидни емулгируеми концентрати
US4107302A (en)	1978-08-15	Novel aqueous insecticidal concentrate composition
HU199244B (en)	1990-02-28	Synergetic fungicide composition
CA1054049A (fr)	1979-05-08	Insecticide liquide concentre
NO156672B (no)	1987-07-27	Preparat med antimikrobiell og eventuelt insekticid virkning og anvendelse av et slikt preparat som tre- og vekstbeskyttelsesmiddel.
HU184676B (en)	1984-09-28	Pesticide preparation containing organic phosphorus compound and pyretroide derivative
US4783457A (en)	1988-11-08	Pest controlling agents
JPS6340163B2 (fr)	1988-08-10
Van Tiel	1952	Improvement of the residual toxicity of DDT solutions by the addition of coumarone resin
US2944932A (en)	1960-07-12	Insect combatting agent
MXPA02007894A (es)	2002-11-29	Mezclas fungicidas.
US4351834A (en)	1982-09-28	Pesticide
EP0373775A2 (fr)	1990-06-20	Insecticides
NZ304965A (en)	1998-09-24	Pesticide formulation containing beta cypermethrin and ethoxylated polyaryl phenol phosphate or sulphate as a surfactant
SU628818A3 (ru)	1978-10-15	Инсектицидное средство
JPS6210202B2 (fr)	1987-03-05
US2676880A (en)	1954-04-27	Herbicidal compositions
JPH0558811A (ja)	1993-03-09	殺虫組成物
US4038394A (en)	1977-07-26	Substituted pyrimido-[4,5-d]-pyrimidine compounds useful for repelling insects, rodents or animals from substrates
DE2211706A1 (de)	1972-09-28	Thiazol-Derivate
Hadaway et al.	1963	Some effects of formulation on the initial contact toxicity of insecticides to adult mosquitos

CA1054049A - Insecticide liquide concentre - Google Patents

Info

Links

Landscapes

Priority Applications (1)

Applications Claiming Priority (1)

Publications (1)

Family

ID=4107305

Family Applications (1)

Country Status (1)

Cited By (1)

Cited By (1)

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