JPH10503500A - 殺虫剤 - Google Patents

殺虫剤

Info

Publication number: JPH10503500A
Authority: JP; Japan
Prior art keywords: group; species; alkyl; formula; active compound
Prior art date: 1994-07-29
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.): Pending

Application number

JP50612896A

Other languages

English (en)

Japanese (ja)

Inventor

クリストフエルデレン，

ボルフガングクレマー，

Original Assignee

バイエル・アクチエンゲゼルシヤフト

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.)

1994-07-29

Filing date

1995-07-17

Publication date

1998-03-31

1995-07-17 Application filed by バイエル・アクチエンゲゼルシヤフト filed Critical バイエル・アクチエンゲゼルシヤフト

1998-03-31 Publication of JPH10503500A publication Critical patent/JPH10503500A/ja

Status Pending legal-status Critical Current

Links

239000002917 insecticide Substances 0.000 title claims abstract description 12
-1 chloronicotinyl Chemical group 0.000 claims abstract description 24
150000002148 esters Chemical class 0.000 claims abstract description 7
ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 claims abstract description 6
125000001424 substituent group Chemical group 0.000 claims abstract description 6
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims abstract description 4
150000007980 azole derivatives Chemical class 0.000 claims abstract description 4
150000001733 carboxylic acid esters Chemical class 0.000 claims abstract description 3
125000005266 diarylamine group Chemical group 0.000 claims abstract description 3
239000002018 neem oil Substances 0.000 claims abstract description 3
150000003014 phosphoric acid esters Chemical class 0.000 claims abstract description 3
239000000203 mixture Substances 0.000 claims description 32
125000000217 alkyl group Chemical group 0.000 claims description 21
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
230000001588 bifunctional effect Effects 0.000 claims description 3
125000006575 electron-withdrawing group Chemical group 0.000 claims description 3
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229910019142 PO4 Inorganic materials 0.000 abstract description 3
HEBMCVBCEDMUOF-UHFFFAOYSA-N isochromane Chemical compound C1=CC=C2COCCC2=C1 HEBMCVBCEDMUOF-UHFFFAOYSA-N 0.000 abstract description 2
239000010452 phosphate Substances 0.000 abstract description 2
239000002253 acid Substances 0.000 abstract 1
150000001408 amides Chemical class 0.000 abstract 1
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ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
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125000000623 heterocyclic group Chemical group 0.000 description 7
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 6
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235000010489 acacia gum Nutrition 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
230000004913 activation Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
210000002534 adenoid Anatomy 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
125000000304 alkynyl group Chemical group 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
239000005667 attractant Substances 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
125000005605 benzo group Chemical group 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
239000001273 butane Substances 0.000 description 1
235000015115 caffè latte Nutrition 0.000 description 1
239000002775 capsule Substances 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
150000003857 carboxamides Chemical class 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000000969 carrier Substances 0.000 description 1
210000000170 cell membrane Anatomy 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000003245 coal Substances 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000002485 combustion reaction Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
UZBQIPPOMKBLAS-UHFFFAOYSA-N diethylazanide Chemical compound CC[N-]CC UZBQIPPOMKBLAS-UHFFFAOYSA-N 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229940096118 ella Drugs 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
230000012173 estrus Effects 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000006260 foam Substances 0.000 description 1
150000003948 formamides Chemical class 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
210000004907 gland Anatomy 0.000 description 1
239000003966 growth inhibitor Substances 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
239000010903 husk Substances 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
150000002466 imines Chemical class 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
239000004579 marble Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
244000005700 microbiome Species 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
239000003595 mist Substances 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
229940042880 natural phospholipid Drugs 0.000 description 1
229920005615 natural polymer Polymers 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
239000006072 paste Substances 0.000 description 1
230000035699 permeability Effects 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
239000002861 polymer material Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
229960003351 prussian blue Drugs 0.000 description 1
239000013225 prussian blue Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000002728 pyrethroid Substances 0.000 description 1
125000000719 pyrrolidinyl group Chemical group 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000011435 rock Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
OOLLAFOLCSJHRE-ZHAKMVSLSA-N ulipristal acetate Chemical compound C1=CC(N(C)C)=CC=C1[C@@H]1C2=C3CCC(=O)C=C3CC[C@H]2[C@H](CC[C@]2(OC(C)=O)C(C)=O)[C@]2(C)C1 OOLLAFOLCSJHRE-ZHAKMVSLSA-N 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003751 zinc Chemical class 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
- A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring

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)

JP50612896A 1994-07-29 1995-07-17 殺虫剤 Pending JPH10503500A (ja)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
DE4426942.0		1994-07-29
DE19944426942 DE4426942A1 (de)	1994-07-29	1994-07-29	Insektizide Mittel
PCT/EP1995/002798 WO1996003879A1 (fr)	1994-07-29	1995-07-17	Insecticides

Publications (1)

Publication Number	Publication Date
JPH10503500A true JPH10503500A (ja)	1998-03-31

Family

ID=6524469

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP50612896A Pending JPH10503500A (ja)	1994-07-29	1995-07-17	殺虫剤

Country Status (5)

Country	Link
EP (1)	EP0804080A1 (fr)
JP (1)	JPH10503500A (fr)
AU (1)	AU3112695A (fr)
DE (1)	DE4426942A1 (fr)
WO (1)	WO1996003879A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2005531567A (ja) *	2002-05-23	2005-10-20	シンジェンタリミテッド	殺虫剤の活性増強剤としてのホスホナート及びその誘導体
JP2007532499A (ja) *	2004-04-07	2007-11-15	バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト	殺虫特性を有する活性成分の組み合わせ

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2729825A1 (fr) *	1995-01-30	1996-08-02	Rhone Poulenc Agrochimie	Associations insecticides comprenant un insecticide de la famille des chloronicotinyls et un insecticide a groupe pyrazole,pyrrole ou phenylimidazole pour traiter les semences ou le sol
DE10059606A1 (de)	2000-12-01	2002-06-06	Bayer Ag	Wirkstoffkombinationen
JP5365160B2 (ja) *	2008-11-25	2013-12-11	住友化学株式会社	有害生物防除用組成物及び有害生物の防除方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4731385A (en) *	1985-10-26	1988-03-15	Nihon Tokushu Noyaku Seizo K.K.	Insecticidal and fungicidal composition for agricultural and horticultural use
JPH0558811A (ja) *	1991-08-27	1993-03-09	Nippon Soda Co Ltd	殺虫組成物
JP3495056B2 (ja) *	1993-03-18	2004-02-09	バイエルクロップサイエンス株式会社	殺虫組成物

1994
- 1994-07-29 DE DE19944426942 patent/DE4426942A1/de not_active Withdrawn
1995
- 1995-07-17 JP JP50612896A patent/JPH10503500A/ja active Pending
- 1995-07-17 AU AU31126/95A patent/AU3112695A/en not_active Abandoned
- 1995-07-17 EP EP95926912A patent/EP0804080A1/fr not_active Withdrawn
- 1995-07-17 WO PCT/EP1995/002798 patent/WO1996003879A1/fr not_active Ceased

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2005531567A (ja) *	2002-05-23	2005-10-20	シンジェンタリミテッド	殺虫剤の活性増強剤としてのホスホナート及びその誘導体
JP2007532499A (ja) *	2004-04-07	2007-11-15	バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト	殺虫特性を有する活性成分の組み合わせ

Also Published As

Publication number	Publication date
WO1996003879A1 (fr)	1996-02-15
AU3112695A (en)	1996-03-04
DE4426942A1 (de)	1996-02-01
EP0804080A1 (fr)	1997-11-05

Publication	Publication Date	Title
JP3963476B2 (ja)	2007-08-22	殺虫剤
CA2146822A1 (fr)	1995-10-15	Melanges insecticides
JPH01160981A (ja)	1989-06-23	１，２，３，４‐テトラヒドロ‐５‐ニトロ‐ピリミジン誘導体
US4288451A (en)	1981-09-08	Combating arthropods with ferrocene-containing synergistic compositions
US4603214A (en)	1986-07-29	Agents for combating pests
US4965254A (en)	1990-10-23	Agents for combating pests
JP2802315B2 (ja)	1998-09-24	害虫防除剤
DE4426942A1 (de)	1996-02-01	Insektizide Mittel
US4656163A (en)	1987-04-07	Compositions and methods of combating pests employing sulphenic acid amides in combination with known nematicides or insecticides
CA1290685C (fr)	1991-10-15	Flubenzimine contenant des agents pour la lutte contre les ravageurs
US5118706A (en)	1992-06-02	Carboximide containing agents for combating pests
DE2928465A1 (de)	1981-01-29	Schaedlingsbekaempfungsmittel
DE3317384A1 (de)	1984-11-15	N-cyancarbonyl-carbamate, verfahren zu ihrer herstellung und ihre verwendung zur schaedlingsbekaempfung
JPH06192280A (ja)	1994-07-12	ホスホリルチオメチルスルホキシド類
DE2637008A1 (de)	1978-02-23	Unsymmetrische 0,0-dialkyl-0-vinylthionophosphorsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide

JPH10503500A - 殺虫剤 - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (3)

Publications (1)

Family

ID=6524469

Family Applications (1)

Country Status (5)

Cited By (2)

Families Citing this family (3)

Family Cites Families (3)

Cited By (2)

Also Published As

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