JP2004352657A - 水田用除草剤組成物 - Google Patents

水田用除草剤組成物 Download PDF

Info

Publication number: JP2004352657A
Authority: JP; Japan
Prior art keywords: alkyl; weight; halo; parts; compound
Prior art date: 2003-05-29
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

JP2003152242A

Other languages

English (en)

Japanese (ja)

Inventor

Keiji Endo

恵次遠藤

Seishi Ito

整志伊藤

Hideji Mukoda

秀司向田

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.)

Bayer CropScience AG

Original Assignee

Bayer CropScience AG

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.)

2003-05-29

Filing date

2003-05-29

Publication date

2004-12-16

2003-05-29 Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG

2003-05-29 Priority to JP2003152242A priority Critical patent/JP2004352657A/ja

2004-05-15 Priority to JP2006529842A priority patent/JP4708349B2/ja

2004-05-15 Priority to CNB2004800146826A priority patent/CN100388885C/zh

2004-05-15 Priority to KR1020057022828A priority patent/KR101180152B1/ko

2004-05-15 Priority to PCT/EP2004/005254 priority patent/WO2004105482A2/fr

2004-12-16 Publication of JP2004352657A publication Critical patent/JP2004352657A/ja

Status Pending legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 51
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239000004009 herbicide Substances 0.000 title abstract description 9
150000001875 compounds Chemical class 0.000 claims abstract description 43
-1 HOK201 Chemical compound 0.000 claims abstract description 30
IHHMUBRVTJMLQO-UHFFFAOYSA-N Pyraclonil Chemical compound C#CCN(C)C1=C(C#N)C=NN1C1=NN(CCCC2)C2=C1Cl IHHMUBRVTJMLQO-UHFFFAOYSA-N 0.000 claims abstract description 7
LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 claims abstract description 5
OEYOMNZEMCPTKN-UHFFFAOYSA-N Butamifos Chemical compound CCC(C)NP(=S)(OCC)OC1=CC(C)=CC=C1[N+]([O-])=O OEYOMNZEMCPTKN-UHFFFAOYSA-N 0.000 claims abstract description 5
VYNOULHXXDFBLU-UHFFFAOYSA-N Cumyluron Chemical compound C=1C=CC=CC=1C(C)(C)NC(=O)NCC1=CC=CC=C1Cl VYNOULHXXDFBLU-UHFFFAOYSA-N 0.000 claims abstract description 5
239000005575 MCPB Substances 0.000 claims abstract description 5
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LVKTWOXHRYGDMM-UHFFFAOYSA-N Naproanilide Chemical compound C=1C=C2C=CC=CC2=CC=1OC(C)C(=O)NC1=CC=CC=C1 LVKTWOXHRYGDMM-UHFFFAOYSA-N 0.000 claims abstract description 5
OBLNWSCLAYSJJR-UHFFFAOYSA-N Quinoclamin Chemical compound C1=CC=C2C(=O)C(N)=C(Cl)C(=O)C2=C1 OBLNWSCLAYSJJR-UHFFFAOYSA-N 0.000 claims abstract description 5
ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 claims abstract description 5
BWUPSGJXXPATLU-UHFFFAOYSA-N dimepiperate Chemical compound C=1C=CC=CC=1C(C)(C)SC(=O)N1CCCCC1 BWUPSGJXXPATLU-UHFFFAOYSA-N 0.000 claims abstract description 5
ASRAWSBMDXVNLX-UHFFFAOYSA-N pyrazolynate Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OS(=O)(=O)C1=CC=C(C)C=C1 ASRAWSBMDXVNLX-UHFFFAOYSA-N 0.000 claims abstract description 5
BDQWWOHKFDSADC-UHFFFAOYSA-N 2-(2,4-dichloro-3-methylphenoxy)-n-phenylpropanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C)OC1=CC=C(Cl)C(C)=C1Cl BDQWWOHKFDSADC-UHFFFAOYSA-N 0.000 claims abstract description 4
239000004480 active ingredient Substances 0.000 claims abstract description 4
RRNIZKPFKNDSRS-UHFFFAOYSA-N Bensulide Chemical compound CC(C)OP(=S)(OC(C)C)SCCNS(=O)(=O)C1=CC=CC=C1 RRNIZKPFKNDSRS-UHFFFAOYSA-N 0.000 claims abstract description 3
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125000004093 cyano group Chemical group *C#N 0.000 claims description 6
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 6
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239000005476 Bentazone Substances 0.000 claims description 4
125000000304 alkynyl group Chemical group 0.000 claims description 4
CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzidamine Natural products C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 claims description 4
XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 claims description 4
RFMQOHXWHFHOJF-UHFFFAOYSA-N cyano thiocyanate Chemical compound N#CSC#N RFMQOHXWHFHOJF-UHFFFAOYSA-N 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
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230000001276 controlling effect Effects 0.000 abstract 1
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RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
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239000007787 solid Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
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235000012239 silicon dioxide Nutrition 0.000 description 3
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XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
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241000064140 Lindernia Species 0.000 description 2
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LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
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150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
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SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
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 2
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WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical class ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
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PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
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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
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238000004381 surface treatment Methods 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
238000002054 transplantation Methods 0.000 description 1
239000002699 waste material Substances 0.000 description 1
238000009333 weeding Methods 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
229940082509 xanthan gum Drugs 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
- 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/10—Sulfones; Sulfoxides

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)

JP2003152242A 2003-05-29 2003-05-29 水田用除草剤組成物 Pending JP2004352657A (ja)

Priority Applications (5)

Application Number	Priority Date	Filing Date	Title
JP2003152242A JP2004352657A (ja)	2003-05-29	2003-05-29	水田用除草剤組成物
JP2006529842A JP4708349B2 (ja)	2003-05-29	2004-05-15	水田用除草剤組成物
CNB2004800146826A CN100388885C (zh)	2003-05-29	2004-05-15	用于稻田的除草组合物
KR1020057022828A KR101180152B1 (ko)	2003-05-29	2004-05-15	논의 제초제 조성물
PCT/EP2004/005254 WO2004105482A2 (fr)	2003-05-29	2004-05-15	Compositions herbicides pour riziere

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP2003152242A JP2004352657A (ja)	2003-05-29	2003-05-29	水田用除草剤組成物

Publications (1)

Publication Number	Publication Date
JP2004352657A true JP2004352657A (ja)	2004-12-16

Family

ID=33487253

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
JP2003152242A Pending JP2004352657A (ja)	2003-05-29	2003-05-29	水田用除草剤組成物
JP2006529842A Expired - Lifetime JP4708349B2 (ja)	2003-05-29	2004-05-15	水田用除草剤組成物

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
JP2006529842A Expired - Lifetime JP4708349B2 (ja)	2003-05-29	2004-05-15	水田用除草剤組成物

Country Status (4)

Country	Link
JP (2)	JP2004352657A (fr)
KR (1)	KR101180152B1 (fr)
CN (1)	CN100388885C (fr)
WO (1)	WO2004105482A2 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2010530382A (ja) *	2007-06-19	2010-09-09	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	稲作に施用するためのベンゾイルシクロヘキサンジオン群からの相乗的作物耐性除草剤の組み合わせ

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB0816880D0 (en) *	2008-09-15	2008-10-22	Syngenta Ltd	Improvements in or relating to organic compounds
JP5622844B2 (ja) *	2009-05-27	2014-11-12	バイエル・クロップサイエンス・アーゲーＢａｙｅｒＣｒｏｐｓｃｉｅｎｃｅＡｇ	稲作に使用するための、テフリルトリオンを含む除草剤混合物
BR112012020709B1 (pt)	2010-02-19	2017-12-19	Bayer Intellectual Property Gmbh	Benzoylcyclohexanodions replaced by 3-aminocarbonyl, composition as comprehending and method for the control of undesired plants
EP3679794A1 (fr)	2019-11-27	2020-07-15	Bayer AG	Compositions herbicides

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19846792A1 (de) *	1998-10-10	2000-04-13	Hoechst Schering Agrevo Gmbh	Benzoylcyclohexandione, Verfahren zur ihrer Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren
DE19950943A1 (de) *	1999-10-22	2001-05-17	Aventis Cropscience Gmbh	Synergistische herbizide Mittel enthaltend Herbizide aus der Gruppe der Hemmstoffe der Hydroxyphenylpyruvat-Dioxygenase
DE10119721A1 (de) *	2001-04-21	2002-10-31	Bayer Cropscience Gmbh	Herbizide Mittel enthaltend Benzoylcyclohexandione und Safener
DE10119728A1 (de) *	2001-04-21	2002-10-31	Bayer Cropscience Gmbh	Synergistische herbizide Mittel enthaltend Herbizide aus der Gruppe der Benzoylcyclohexandione für den Einsatz in Reis-Kulturen

2003
- 2003-05-29 JP JP2003152242A patent/JP2004352657A/ja active Pending
2004
- 2004-05-15 CN CNB2004800146826A patent/CN100388885C/zh not_active Expired - Lifetime
- 2004-05-15 WO PCT/EP2004/005254 patent/WO2004105482A2/fr not_active Ceased
- 2004-05-15 JP JP2006529842A patent/JP4708349B2/ja not_active Expired - Lifetime
- 2004-05-15 KR KR1020057022828A patent/KR101180152B1/ko not_active Expired - Lifetime

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2010530382A (ja) *	2007-06-19	2010-09-09	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	稲作に施用するためのベンゾイルシクロヘキサンジオン群からの相乗的作物耐性除草剤の組み合わせ

Also Published As

Publication number	Publication date
WO2004105482A2 (fr)	2004-12-09
JP2007502849A (ja)	2007-02-15
KR101180152B1 (ko)	2012-09-05
KR20060015323A (ko)	2006-02-16
CN1794912A (zh)	2006-06-28
JP4708349B2 (ja)	2011-06-22
WO2004105482A3 (fr)	2005-04-07
CN100388885C (zh)	2008-05-21

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JP2010530382A (ja)	2010-09-09	稲作に施用するためのベンゾイルシクロヘキサンジオン群からの相乗的作物耐性除草剤の組み合わせ
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HU188843B (en)	1986-05-28	Synergetic herbicidal composition comprising benzothiazolyl-oxy-acetamide-derivative and thiolcarbamate-derivative as active substance
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JP2004352657A - 水田用除草剤組成物 - Google Patents

Info

Links

Classifications

Landscapes

Priority Applications (5)

Applications Claiming Priority (1)

Publications (1)

Family

ID=33487253

Family Applications (2)

Family Applications After (1)

Country Status (4)

Cited By (1)

Families Citing this family (4)

Family Cites Families (4)

Cited By (1)

Also Published As

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