HRP20040337B1 - Herbicidal mixtures based on 3-phenyluracils - Google Patents
Herbicidal mixtures based on 3-phenyluracilsInfo
- Publication number
- HRP20040337B1 HRP20040337B1 HR20040337A HRP20040337A HRP20040337B1 HR P20040337 B1 HRP20040337 B1 HR P20040337B1 HR 20040337 A HR20040337 A HR 20040337A HR P20040337 A HRP20040337 A HR P20040337A HR P20040337 B1 HRP20040337 B1 HR P20040337B1
- Authority
- HR
- Croatia
- Prior art keywords
- inhibitors
- alkyl
- herbicides
- alkoxy
- halogen
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 14
- -1 phenyluracil compound Chemical class 0.000 abstract 9
- 239000004009 herbicide Substances 0.000 abstract 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229910052736 halogen Chemical group 0.000 abstract 3
- 150000002367 halogens Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 229930192334 Auxin Natural products 0.000 abstract 2
- 239000002363 auxin Substances 0.000 abstract 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 150000004669 very long chain fatty acids Chemical class 0.000 abstract 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- HKELWJONQIFBPO-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-5-(trichloromethyl)-1,2,4-triazole-3-carboxylic acid Chemical compound N1=C(C(=O)O)N=C(C(Cl)(Cl)Cl)N1C1=CC=C(Cl)C=C1Cl HKELWJONQIFBPO-UHFFFAOYSA-N 0.000 abstract 1
- XEJNEDVTJPXRSM-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-5-methyl-4,5-dihydro-1H-pyrazole-3,5-dicarboxylic acid Chemical compound OC(=O)C1(C)CC(C(O)=O)=NN1C1=CC=C(Cl)C=C1Cl XEJNEDVTJPXRSM-UHFFFAOYSA-N 0.000 abstract 1
- QWWHRELOCZEQNZ-UHFFFAOYSA-N 2,2-dichloro-1-(1-oxa-4-azaspiro[4.5]decan-4-yl)ethanone Chemical compound ClC(Cl)C(=O)N1CCOC11CCCCC1 QWWHRELOCZEQNZ-UHFFFAOYSA-N 0.000 abstract 1
- CZSMRBVLOVGPLX-UHFFFAOYSA-N 2,2-dichloro-1-(2,2,4-trimethyl-1,3-oxazolidin-3-yl)ethanone Chemical compound CC1COC(C)(C)N1C(=O)C(Cl)Cl CZSMRBVLOVGPLX-UHFFFAOYSA-N 0.000 abstract 1
- MCNOFYBITGAAGM-UHFFFAOYSA-N 2,2-dichloro-1-[5-(furan-2-yl)-2,2-dimethyl-1,3-oxazolidin-3-yl]ethanone Chemical compound C1N(C(=O)C(Cl)Cl)C(C)(C)OC1C1=CC=CO1 MCNOFYBITGAAGM-UHFFFAOYSA-N 0.000 abstract 1
- WZZRJCUYSKKFHO-UHFFFAOYSA-N 2-(n-benzoyl-3,4-dichloroanilino)propanoic acid Chemical compound C=1C=C(Cl)C(Cl)=CC=1N(C(C)C(O)=O)C(=O)C1=CC=CC=C1 WZZRJCUYSKKFHO-UHFFFAOYSA-N 0.000 abstract 1
- SVOAUHHKPGKPQK-UHFFFAOYSA-N 2-chloro-9-hydroxyfluorene-9-carboxylic acid Chemical compound C1=C(Cl)C=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 SVOAUHHKPGKPQK-UHFFFAOYSA-N 0.000 abstract 1
- WBFYVDCHGVNRBH-UHFFFAOYSA-N 7,8-dihydropteroic acid Chemical compound N=1C=2C(=O)NC(N)=NC=2NCC=1CNC1=CC=C(C(O)=O)C=C1 WBFYVDCHGVNRBH-UHFFFAOYSA-N 0.000 abstract 1
- 108010000700 Acetolactate synthase Proteins 0.000 abstract 1
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 abstract 1
- 239000005644 Dazomet Substances 0.000 abstract 1
- YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 abstract 1
- ICWUMLXQKFTJMH-UHFFFAOYSA-N Etobenzanid Chemical compound C1=CC(OCOCC)=CC=C1C(=O)NC1=CC=CC(Cl)=C1Cl ICWUMLXQKFTJMH-UHFFFAOYSA-N 0.000 abstract 1
- YQVMVCCFZCMYQB-UHFFFAOYSA-N Flamprop Chemical compound C=1C=C(F)C(Cl)=CC=1N(C(C)C(O)=O)C(=O)C1=CC=CC=C1 YQVMVCCFZCMYQB-UHFFFAOYSA-N 0.000 abstract 1
- YQVMVCCFZCMYQB-SNVBAGLBSA-N Flamprop-M Chemical compound C=1C=C(F)C(Cl)=CC=1N([C@H](C)C(O)=O)C(=O)C1=CC=CC=C1 YQVMVCCFZCMYQB-SNVBAGLBSA-N 0.000 abstract 1
- 239000002169 Metam Substances 0.000 abstract 1
- FMINYZXVCTYSNY-UHFFFAOYSA-N Methyldymron Chemical compound C=1C=CC=CC=1N(C)C(=O)NC(C)(C)C1=CC=CC=C1 FMINYZXVCTYSNY-UHFFFAOYSA-N 0.000 abstract 1
- IUFUITYPUYMIHI-UHFFFAOYSA-N N-[1-(3,5-dimethylphenoxy)propan-2-yl]-6-(2-fluoropropan-2-yl)-1,3,5-triazine-2,4-diamine Chemical compound N=1C(N)=NC(C(C)(C)F)=NC=1NC(C)COC1=CC(C)=CC(C)=C1 IUFUITYPUYMIHI-UHFFFAOYSA-N 0.000 abstract 1
- 108020001991 Protoporphyrinogen Oxidase Proteins 0.000 abstract 1
- 102000005135 Protoporphyrinogen oxidase Human genes 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- OTSAMNSACVKIOJ-UHFFFAOYSA-N azane;carbamoyl(ethoxy)phosphinic acid Chemical compound [NH4+].CCOP([O-])(=O)C(N)=O OTSAMNSACVKIOJ-UHFFFAOYSA-N 0.000 abstract 1
- MKQSWTQPLLCSOB-UHFFFAOYSA-N benzyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate Chemical compound N1=C(Cl)SC(C(=O)OCC=2C=CC=CC=2)=C1C(F)(F)F MKQSWTQPLLCSOB-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 238000004061 bleaching Methods 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 230000008166 cellulose biosynthesis Effects 0.000 abstract 1
- ICJSJAJWTWPSBD-UHFFFAOYSA-N cloquintocet Chemical compound C1=CN=C2C(OCC(=O)O)=CC=C(Cl)C2=C1 ICJSJAJWTWPSBD-UHFFFAOYSA-N 0.000 abstract 1
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 abstract 1
- XXWNKVBJDWSYBN-UHFFFAOYSA-N diethoxy-phenoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(=S)(OCC)OC1=CC=CC=C1 XXWNKVBJDWSYBN-UHFFFAOYSA-N 0.000 abstract 1
- QMTNOLKHSWIQBE-FGTMMUONSA-N exo-(+)-cinmethylin Chemical compound O([C@H]1[C@]2(C)CC[C@@](O2)(C1)C(C)C)CC1=CC=CC=C1C QMTNOLKHSWIQBE-FGTMMUONSA-N 0.000 abstract 1
- 239000003188 fatty acid synthesis inhibitor Substances 0.000 abstract 1
- 102000005396 glutamine synthetase Human genes 0.000 abstract 1
- 108020002326 glutamine synthetase Proteins 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- ITGSCCPVERXFGN-UHFFFAOYSA-N isoxadifen Chemical compound C1C(C(=O)O)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 ITGSCCPVERXFGN-UHFFFAOYSA-N 0.000 abstract 1
- 150000002632 lipids Chemical class 0.000 abstract 1
- HYVVJDQGXFXBRZ-UHFFFAOYSA-N metam Chemical compound CNC(S)=S HYVVJDQGXFXBRZ-UHFFFAOYSA-N 0.000 abstract 1
- 229940102396 methyl bromide Drugs 0.000 abstract 1
- 230000011278 mitosis Effects 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Chemical group 0.000 abstract 1
- 230000029553 photosynthesis Effects 0.000 abstract 1
- 238000010672 photosynthesis Methods 0.000 abstract 1
- VTRWMTJQBQJKQH-UHFFFAOYSA-N pyributicarb Chemical compound COC1=CC=CC(N(C)C(=S)OC=2C=C(C=CC=2)C(C)(C)C)=N1 VTRWMTJQBQJKQH-UHFFFAOYSA-N 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- QYOJSKGCWNAKGW-HCWXCVPCSA-N shikimate-3-phosphate Chemical compound O[C@H]1CC(C(O)=O)=C[C@H](OP(O)(O)=O)[C@@H]1O QYOJSKGCWNAKGW-HCWXCVPCSA-N 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 229910052717 sulfur Chemical group 0.000 abstract 1
- 239000011593 sulfur Chemical group 0.000 abstract 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
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
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)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31883401P | 2001-09-14 | 2001-09-14 | |
US33313501P | 2001-11-27 | 2001-11-27 | |
PCT/EP2002/010136 WO2003024221A1 (en) | 2001-09-14 | 2002-09-10 | Herbicidal mixtures based on 3-phenyluracils |
Publications (2)
Publication Number | Publication Date |
---|---|
HRP20040337A2 HRP20040337A2 (en) | 2004-10-31 |
HRP20040337B1 true HRP20040337B1 (en) | 2007-09-30 |
Family
ID=26981697
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HR20040337A HRP20040337B1 (en) | 2001-09-14 | 2004-04-13 | Herbicidal mixtures based on 3-phenyluracils |
Country Status (28)
Country | Link |
---|---|
US (1) | US7375058B2 (zh) |
EP (1) | EP1429609B1 (zh) |
JP (1) | JP4237622B2 (zh) |
KR (1) | KR100974124B1 (zh) |
CN (1) | CN100493354C (zh) |
AR (1) | AR036523A1 (zh) |
AT (1) | ATE355747T1 (zh) |
BR (1) | BR0212460A (zh) |
CA (1) | CA2460088C (zh) |
DE (1) | DE60218707T2 (zh) |
DK (1) | DK1429609T3 (zh) |
EA (1) | EA006546B1 (zh) |
ES (1) | ES2281550T3 (zh) |
GE (1) | GEP20063907B (zh) |
HR (1) | HRP20040337B1 (zh) |
HU (1) | HU228904B1 (zh) |
IL (2) | IL160485A0 (zh) |
ME (1) | MEP7108A (zh) |
MX (1) | MXPA04002087A (zh) |
NO (1) | NO330553B1 (zh) |
NZ (1) | NZ531486A (zh) |
PL (1) | PL209105B1 (zh) |
PT (1) | PT1429609E (zh) |
RS (1) | RS50828B (zh) |
TW (1) | TWI252078B (zh) |
UY (1) | UY27447A1 (zh) |
WO (1) | WO2003024221A1 (zh) |
ZA (1) | ZA200402791B (zh) |
Families Citing this family (106)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10163079A1 (de) | 2001-12-20 | 2003-07-03 | Basf Ag | Verfahren zur Verbesserung des Pflanzenwachstums durch Applikation einer Mischung aus Schwefel und Komplexbildner |
PL371445A1 (en) * | 2002-03-21 | 2005-06-13 | Syngenta Participations Ag | Herbicidal composition |
US20060293187A1 (en) * | 2003-03-13 | 2006-12-28 | Basf Aktiengesellschaft | Herbicidal mixtures based on 3-phenyluracils |
DE10334300A1 (de) * | 2003-07-28 | 2005-03-03 | Bayer Cropscience Gmbh | Ölsuspensionskonzentrat |
ATE381547T1 (de) * | 2003-12-03 | 2008-01-15 | Basf Ag | Verfahren zur herstellung von 3- phenyl(thio)uracilen und 3-phenyldithiouracilen |
JP4736480B2 (ja) * | 2004-05-17 | 2011-07-27 | 住友化学株式会社 | 雑草防除方法 |
WO2006005490A2 (en) * | 2004-07-09 | 2006-01-19 | Basf Aktiengesellschaft | A method for controlling coniferous plants |
MY144905A (en) * | 2005-03-17 | 2011-11-30 | Basf Ag | Herbicidal compositions based on 3-phenyluracils and 3-sulfonylisoxazolines |
JP4696663B2 (ja) * | 2005-04-26 | 2011-06-08 | 住友化学株式会社 | 除草用組成物 |
AU2006251185B2 (en) * | 2005-05-24 | 2011-04-07 | Basf Aktiengesellschaft | Method for production of 1-alkyl-3-phenyluracils |
AR056436A1 (es) * | 2005-08-01 | 2007-10-10 | Basf Ag | Un metodo para controlar malezas |
AR056437A1 (es) * | 2005-08-01 | 2007-10-10 | Basf Ag | Un metodo para desecar y/o desfoliar cultivos resistentes a glifosfato |
AR056438A1 (es) * | 2005-08-01 | 2007-10-10 | Basf Ag | Un metodo para controlar malezas |
AR055593A1 (es) * | 2005-08-01 | 2007-08-29 | Basf Ag | Un metodo para controlar malezas |
UA90757C2 (ru) * | 2005-10-12 | 2010-05-25 | Басф Се | Гербицидная композиция, способ борьбы с нежелательной растительностью и способ защиты посевов от фитотоксичного действия 3-фенилурацилов |
BRPI0712484B1 (pt) | 2006-06-06 | 2017-06-06 | Monsanto Technology Llc | método para seleção de células transformadas |
US7855326B2 (en) | 2006-06-06 | 2010-12-21 | Monsanto Technology Llc | Methods for weed control using plants having dicamba-degrading enzymatic activity |
US7838729B2 (en) | 2007-02-26 | 2010-11-23 | Monsanto Technology Llc | Chloroplast transit peptides for efficient targeting of DMO and uses thereof |
CN101677561B (zh) * | 2007-04-09 | 2014-03-12 | 诺维信生物股份有限公司 | 使用Thaxtomin与Thaxtomin组合物控制藻类的方法 |
GB0721689D0 (en) * | 2007-11-05 | 2007-12-12 | Syngenta Ltd | Herbicidal compositions |
WO2009089165A2 (en) * | 2008-01-07 | 2009-07-16 | Auburn University | Combinations of herbicides and safeners |
EP2254418A2 (en) * | 2008-02-12 | 2010-12-01 | Arysta LifeScience North America, LLC | Method of controlling unwanted vegetation |
DE102008037631A1 (de) * | 2008-08-14 | 2010-02-18 | Bayer Cropscience Ag | Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden |
CN104789649A (zh) | 2009-01-07 | 2015-07-22 | 巴斯夫农化产品有限公司 | 大豆事件127和与其相关的方法 |
US8927551B2 (en) | 2009-05-18 | 2015-01-06 | Infinity Pharmaceuticals, Inc. | Isoxazolines as inhibitors of fatty acid amide hydrolase |
US8765735B2 (en) | 2009-05-18 | 2014-07-01 | Infinity Pharmaceuticals, Inc. | Isoxazolines as inhibitors of fatty acid amide hydrolase |
US9149465B2 (en) | 2009-05-18 | 2015-10-06 | Infinity Pharmaceuticals, Inc. | Isoxazolines as inhibitors of fatty acid amide hydrolase |
US8778838B2 (en) * | 2009-08-27 | 2014-07-15 | Basf Se | Aqueous concentrate formulations containing saflufenacil and glyphosate |
BR112012004057A2 (pt) | 2009-08-27 | 2019-09-24 | Basf Se | formulação de concentrado em suspensão aquoso da formulação de concentrado em suspensão aquoso e metodo para controlar vegetação indesejada |
CN102027913B (zh) * | 2009-09-28 | 2013-09-18 | 南京华洲药业有限公司 | 一种含氟硫草定与绿草定的除草组合物及其应用 |
CN102651971B (zh) * | 2009-12-09 | 2015-05-13 | 巴斯夫欧洲公司 | 含有苯嘧磺草胺和草甘膦的液体悬浮浓缩物配制剂 |
US8703650B2 (en) | 2009-12-09 | 2014-04-22 | Basf Se | Liquid suspension concentrate formulations containing saflufenacil |
BR112012021495B1 (pt) * | 2010-02-26 | 2018-08-28 | Bayer Ip Gmbh | combinação herbicida contendo os hidratos de saflufenacil e glifosato ou glufosinato e seus usos |
CN102265883B (zh) * | 2010-06-03 | 2013-08-07 | 南京华洲药业有限公司 | 一种含灭草松、玉嘧磺隆和硝磺草酮的混合除草剂及其应用 |
CN102958361A (zh) * | 2010-06-24 | 2013-03-06 | 巴斯夫欧洲公司 | 除草组合物 |
JP5927007B2 (ja) * | 2011-04-11 | 2016-05-25 | 石原産業株式会社 | 除草組成物 |
PE20160668A1 (es) * | 2013-10-23 | 2016-07-15 | Ishihara Sangyo Kaisha | Composicion herbicida |
WO2015091642A1 (en) | 2013-12-19 | 2015-06-25 | BASF Agro B.V. | Dilute aqueous compositions of saflufenacil |
US9545109B2 (en) * | 2014-08-28 | 2017-01-17 | Sumitomo Chemical Company, Limited | Herbicidal composition |
JP6783236B2 (ja) | 2015-01-15 | 2020-11-11 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | サフルフェナシル及びグルホシネートを含む除草剤の組合せ |
CA2973915C (en) * | 2015-01-22 | 2024-01-16 | BASF Agro B.V. | Ternary herbicidal combination comprising saflufenacil |
CN106135216A (zh) * | 2015-04-24 | 2016-11-23 | 江苏龙灯化学有限公司 | 除草剂组合物 |
CN106135226B (zh) * | 2015-04-24 | 2021-05-18 | 江苏龙灯化学有限公司 | 一种除草组合物 |
CN106135215A (zh) * | 2015-04-24 | 2016-11-23 | 江苏龙灯化学有限公司 | 除草组合物 |
CN110583678A (zh) * | 2015-04-24 | 2019-12-20 | 江苏龙灯化学有限公司 | 复配除草剂组合物 |
CN104886066A (zh) * | 2015-06-17 | 2015-09-09 | 广东中迅农科股份有限公司 | 一种用于防除非耕地杂草的除草组合物 |
WO2017009134A1 (en) * | 2015-07-10 | 2017-01-19 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific non-accase lipid synthesis inhibitors |
WO2017009142A1 (en) | 2015-07-10 | 2017-01-19 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific pigment synthesis inhibitors |
SI3319437T1 (sl) | 2015-07-10 | 2019-08-30 | BASF Agro B.V. | Herbicidni sestavek, ki vsebuje cinmetilin in piroksasulfon |
EA201890270A1 (ru) | 2015-07-10 | 2018-08-31 | Басф Агро Б.В. | Гербицидная композиция, которая содержит цинметилин и специфические хинолинкарбоновые кислоты |
US20180192647A1 (en) | 2015-07-10 | 2018-07-12 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and acetochlor or pretilachlor |
AU2016294453B2 (en) * | 2015-07-10 | 2020-09-17 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific inhibitors of protoporphyrinogen oxidase |
AU2016292524B2 (en) | 2015-07-10 | 2020-05-28 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and saflufenacil |
US11219215B2 (en) * | 2015-07-10 | 2022-01-11 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific inhibitors of protoporphyrinogen oxidase |
US11219212B2 (en) | 2015-07-10 | 2022-01-11 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and imazamox |
EP3162209A1 (en) * | 2015-10-27 | 2017-05-03 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and imazamox |
PL3319427T3 (pl) | 2015-07-10 | 2020-05-18 | BASF Agro B.V. | Kompozycja chwastobójcza zawierająca cynmetalinę i dimetenamid |
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US5084084A (en) | 1989-07-14 | 1992-01-28 | Nissan Chemical Industries Ltd. | Uracil derivatives and herbicides containing the same as active ingredient |
DE4329537A1 (de) | 1993-09-02 | 1995-03-09 | Basf Ag | Substituierte 1-Amino-3-phenyluracile |
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DE19617532A1 (de) * | 1996-05-02 | 1997-11-06 | Bayer Ag | Substituierte Phenyluracile |
US6444613B1 (en) * | 1999-03-12 | 2002-09-03 | Hoechst Schering Agrevo Gmbh | Defoliant |
DE19927612A1 (de) | 1999-06-17 | 2000-12-21 | Bayer Ag | Substituierte Phenyluracile |
DE19954312A1 (de) | 1999-11-11 | 2001-05-17 | Bayer Ag | Substituierte Phenyluracile |
DE19958381A1 (de) * | 1999-12-03 | 2001-06-07 | Bayer Ag | Herbizide auf Basis von N-Aryl-uracilen |
DE60139107D1 (en) * | 2000-05-04 | 2009-08-13 | Basf Se | Substituierte phenyl-sulfamoyl-carboxamide |
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