HRP20040055A2 - Herbicidal combinations with particular sulphonyl ureas - Google Patents
Herbicidal combinations with particular sulphonyl ureas Download PDFInfo
- Publication number
- HRP20040055A2 HRP20040055A2 HR20040055A HRP20040055A HRP20040055A2 HR P20040055 A2 HRP20040055 A2 HR P20040055A2 HR 20040055 A HR20040055 A HR 20040055A HR P20040055 A HRP20040055 A HR P20040055A HR P20040055 A2 HRP20040055 A2 HR P20040055A2
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- Croatia
- Prior art keywords
- plants
- plant
- acid
- herbicides
- application
- Prior art date
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- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 38
- -1 sulphonyl ureas Chemical class 0.000 title description 21
- 235000013877 carbamide Nutrition 0.000 title 1
- 150000003839 salts Chemical class 0.000 claims abstract description 43
- 239000004009 herbicide Substances 0.000 claims abstract description 42
- 150000001875 compounds Chemical class 0.000 claims abstract description 41
- RBSXHDIPCIWOMG-UHFFFAOYSA-N 1-(4,6-dimethoxypyrimidin-2-yl)-3-(2-ethylsulfonylimidazo[1,2-a]pyridin-3-yl)sulfonylurea Chemical compound CCS(=O)(=O)C=1N=C2C=CC=CN2C=1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 RBSXHDIPCIWOMG-UHFFFAOYSA-N 0.000 claims abstract description 5
- RXCPQSJAVKGONC-UHFFFAOYSA-N Flumetsulam Chemical compound N1=C2N=C(C)C=CN2N=C1S(=O)(=O)NC1=C(F)C=CC=C1F RXCPQSJAVKGONC-UHFFFAOYSA-N 0.000 claims abstract description 5
- AOQMRUTZEYVDIL-UHFFFAOYSA-N Flupoxam Chemical compound C=1C=C(Cl)C(COCC(F)(F)C(F)(F)F)=CC=1N1N=C(C(=O)N)N=C1C1=CC=CC=C1 AOQMRUTZEYVDIL-UHFFFAOYSA-N 0.000 claims abstract description 5
- LXKOADMMGWXPJQ-UHFFFAOYSA-N Halosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=C(Cl)C=2C(O)=O)C)=N1 LXKOADMMGWXPJQ-UHFFFAOYSA-N 0.000 claims abstract description 5
- DDBMQDADIHOWIC-UHFFFAOYSA-N aclonifen Chemical compound C1=C([N+]([O-])=O)C(N)=C(Cl)C(OC=2C=CC=CC=2)=C1 DDBMQDADIHOWIC-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
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 claims abstract description 5
- IANUJLZYFUDJIH-UHFFFAOYSA-N flufenacet Chemical compound C=1C=C(F)C=CC=1N(C(C)C)C(=O)COC1=NN=C(C(F)(F)F)S1 IANUJLZYFUDJIH-UHFFFAOYSA-N 0.000 claims abstract description 5
- NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 claims abstract description 5
- NYRMIJKDBAQCHC-UHFFFAOYSA-N 5-(methylamino)-2-phenyl-4-[3-(trifluoromethyl)phenyl]furan-3(2H)-one Chemical compound O1C(NC)=C(C=2C=C(C=CC=2)C(F)(F)F)C(=O)C1C1=CC=CC=C1 NYRMIJKDBAQCHC-UHFFFAOYSA-N 0.000 claims abstract description 4
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- JTHMVYBOQLDDIY-UHFFFAOYSA-N methyl 2-[(4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carbonyl)sulfamoyl]benzoate Chemical compound O=C1N(C)C(OCCC)=NN1C(=O)NS(=O)(=O)C1=CC=CC=C1C(=O)OC JTHMVYBOQLDDIY-UHFFFAOYSA-N 0.000 claims abstract description 4
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 claims abstract description 4
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- CWKFPEBMTGKLKX-UHFFFAOYSA-N picolinafen Chemical compound C1=CC(F)=CC=C1NC(=O)C1=CC=CC(OC=2C=C(C=CC=2)C(F)(F)F)=N1 CWKFPEBMTGKLKX-UHFFFAOYSA-N 0.000 claims abstract description 3
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- WWHBBYNEFXJGME-UHFFFAOYSA-N ethyl 5-tert-butyl-1-(2,4-dichlorophenyl)pyrazole-3-carboxylate Chemical compound N1=C(C(=O)OCC)C=C(C(C)(C)C)N1C1=CC=C(Cl)C=C1Cl WWHBBYNEFXJGME-UHFFFAOYSA-N 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
- 238000002474 experimental method Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- LYINKTVZUSKQEQ-UHFFFAOYSA-N furan-3-one Chemical compound O=C1COC=C1 LYINKTVZUSKQEQ-UHFFFAOYSA-N 0.000 description 1
- 230000002068 genetic effect Effects 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 239000003673 groundwater Substances 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 231100000001 growth retardation Toxicity 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 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 description 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- LNSXXOLAIATXPJ-UHFFFAOYSA-N methyl 2-[(4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carbonyl)sulfamoyl]benzoate;sodium Chemical compound [Na].O=C1N(C)C(OCCC)=NN1C(=O)NS(=O)(=O)C1=CC=CC=C1C(=O)OC LNSXXOLAIATXPJ-UHFFFAOYSA-N 0.000 description 1
- JPQFAGRIXLICKL-UHFFFAOYSA-N methyl 2-[carbamoyl-(4,6-dimethoxypyrimidin-2-yl)sulfamoyl]-6-(trifluoromethyl)pyridine-3-carboxylate;sodium Chemical compound [Na].COC(=O)C1=CC=C(C(F)(F)F)N=C1S(=O)(=O)N(C(N)=O)C1=NC(OC)=CC(OC)=N1 JPQFAGRIXLICKL-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- VOEYXMAFNDNNED-UHFFFAOYSA-N metolcarb Chemical compound CNC(=O)OC1=CC=CC(C)=C1 VOEYXMAFNDNNED-UHFFFAOYSA-N 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000010369 molecular cloning Methods 0.000 description 1
- 238000002703 mutagenesis Methods 0.000 description 1
- 231100000350 mutagenesis Toxicity 0.000 description 1
- GVBHRBMWXDCRHZ-UHFFFAOYSA-N n-phenylpyridine-2-carboxamide Chemical compound C=1C=CC=NC=1C(=O)NC1=CC=CC=C1 GVBHRBMWXDCRHZ-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 229920002113 octoxynol Polymers 0.000 description 1
- 239000012053 oil suspension Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000002018 overexpression Effects 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 235000020030 perry Nutrition 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000003090 pesticide formulation Substances 0.000 description 1
- LCPDWSOZIOUXRV-UHFFFAOYSA-N phenoxyacetic acid Chemical class OC(=O)COC1=CC=CC=C1 LCPDWSOZIOUXRV-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000010773 plant oil Substances 0.000 description 1
- 239000004476 plant protection product Substances 0.000 description 1
- 239000013612 plasmid Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001522 polyglycol ester Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 238000001243 protein synthesis Methods 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 108091092562 ribozyme Proteins 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000004550 soluble concentrate Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000000565 sulfonamide group Chemical group 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
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 (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10135641A DE10135641A1 (de) | 2001-07-21 | 2001-07-21 | Herbizid-Kombinationen mit speziellen Sulfonylharnstoffen |
| PCT/EP2002/007795 WO2003009684A2 (de) | 2001-07-21 | 2002-07-12 | Herbizid-kombinationen mit speziellen sulfonylharnstoffen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20040055A2 true HRP20040055A2 (en) | 2004-06-30 |
Family
ID=7692672
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HR20040055A HRP20040055A2 (en) | 2001-07-21 | 2004-01-20 | Herbicidal combinations with particular sulphonyl ureas |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US20030050193A1 (ru) |
| EP (1) | EP1418812B1 (ru) |
| AT (1) | ATE347806T1 (ru) |
| AU (1) | AU2002355175A1 (ru) |
| DE (2) | DE10135641A1 (ru) |
| EA (1) | EA007329B1 (ru) |
| HR (1) | HRP20040055A2 (ru) |
| HU (1) | HUP0401489A3 (ru) |
| NO (1) | NO20040265L (ru) |
| PL (1) | PL368678A1 (ru) |
| RS (1) | RS34104A (ru) |
| UA (1) | UA78514C2 (ru) |
| WO (1) | WO2003009684A2 (ru) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10135642A1 (de) * | 2001-07-21 | 2003-02-27 | Bayer Cropscience Gmbh | Herbizid-Kombinationen mit speziellen Sulfonylharnstoffen |
| DE10209478A1 (de) * | 2002-03-05 | 2003-09-18 | Bayer Cropscience Gmbh | Herbizid-Kombinationen mit speziellen Sulfonylharnstoffen |
| EP1545212B1 (en) * | 2002-08-08 | 2008-10-29 | Syngenta Participations AG | Herbicidal composition |
| DE10344919B8 (de) * | 2003-09-17 | 2015-04-09 | K. D. Pharma Bexbach Gmbh | Herbizidwirksames Präparat, Verwendung von bei der Biodieselherstellung anfallendem Glycerin, Verfahren zur Herstellung eines herbizidwirksamen Präparates |
| AR048441A1 (es) | 2004-03-26 | 2006-04-26 | Syngenta Participations Ag | Una combinacion herbicida |
| ZA200802442B (en) * | 2005-09-01 | 2010-02-24 | Du Pont | Liquid sulfonylurea herbicide formulations |
| EP1925203A1 (de) * | 2006-11-13 | 2008-05-28 | Bayer CropScience AG | Herbizid-Kombinationen enthaltend Amidosulfuron und ein Pyridinherbizid |
| WO2009089165A2 (en) * | 2008-01-07 | 2009-07-16 | Auburn University | Combinations of herbicides and safeners |
| RU2010134763A (ru) * | 2008-02-12 | 2012-03-20 | Ариста Лайфсайенс Норс Америка, Ллс (Us) | Способ контроля нежелательной вегетации |
| CN102326574B (zh) * | 2011-07-11 | 2014-08-13 | 陕西美邦农药有限公司 | 一种含双氟磺草胺与磺酰脲类的除草组合物 |
| CN102388899B (zh) * | 2011-09-23 | 2014-03-19 | 合肥星宇化学有限责任公司 | 一种除草组合物及其制剂 |
| CN103404529A (zh) * | 2012-01-16 | 2013-11-27 | 河北博嘉农业有限公司 | 氟唑磺隆复配除草剂 |
| CN102428945A (zh) * | 2012-01-16 | 2012-05-02 | 河北博嘉农业有限公司 | 氟唑磺隆复配除草剂 |
| CN103210947A (zh) * | 2013-05-10 | 2013-07-24 | 步康明 | 含氟唑磺隆的麦田除草剂组合物 |
| CN105557734A (zh) * | 2015-12-11 | 2016-05-11 | 汤云鹤 | 一种含氟唑磺隆和丙草胺的农药组合物及其在防治小麦田杂草中的应用 |
| CN105557732A (zh) * | 2015-12-11 | 2016-05-11 | 汤云鹤 | 一种含氟唑磺隆、氟噻草胺和双氟磺草胺的农药组合物及其在防治小麦田杂草中的应用 |
| CN105557730B (zh) * | 2015-12-11 | 2019-02-12 | 汤云鹤 | 一种含氟唑磺隆、丙草胺和双氟磺草胺的农药组合物及其应用 |
| ES2881573T3 (es) * | 2015-12-23 | 2021-11-29 | Rotam Agrochem Int Co Ltd | Método de control del crecimiento de plantas tolerantes a ALS |
| CN111194167A (zh) * | 2017-10-10 | 2020-05-22 | 美国陶氏益农公司 | 双氟磺草胺的制备方法 |
| WO2020172305A1 (en) | 2019-02-19 | 2020-08-27 | Gowan Company, L.L.C. | Stable liquid compositions and methods of using the same |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3918287A1 (de) * | 1989-06-05 | 1990-12-06 | Hoechst Ag | Herbizide mittel |
| RO117587B1 (ro) * | 1991-07-12 | 2002-05-30 | Hoechst Ag | Compozitie erbicida, procedeu de obtinere a acesteia si metoda pentru controlul plantelor nedorite |
| DE4223465A1 (de) * | 1992-07-16 | 1994-01-20 | Bayer Ag | Herbizide Mittel auf Basis von Heteroaryloxyacetamiden |
| CN1074646C (zh) * | 1992-10-06 | 2001-11-14 | 国际壳牌研究有限公司 | 除草剂混合物 |
| DE19638887A1 (de) * | 1996-09-23 | 1998-03-26 | Bayer Ag | Selektive Herbizide auf Basis von Arylsulfonylaminocarbonyltriazolinonen |
| JP2000038307A (ja) * | 1998-07-23 | 2000-02-08 | Sumitomo Chem Co Ltd | 除草剤組成物 |
| US6114283A (en) * | 1998-07-28 | 2000-09-05 | E. I. Du Pont De Nemours And Company | Herbicidal mixtures |
| DK1104239T3 (da) * | 1998-08-13 | 2004-06-21 | Bayer Cropscience Gmbh | Herbicide midler med acylerede aminophenylsulfonylurinstoffer |
| DE19915013A1 (de) * | 1999-04-01 | 1999-08-26 | Novartis Ag | Herbizides Mittel |
| US6849578B1 (en) * | 1999-11-17 | 2005-02-01 | Bayer Aktiengesellschaft | Selective herbicides based on 2,6-disubstituted pyridine derivatives |
| RU2002116229A (ru) * | 1999-11-18 | 2004-01-20 | Байер Акциенгезелльшафт (De) | Синергетически гербицидные комбинации активных веществ |
| TWI243019B (en) * | 2000-08-31 | 2005-11-11 | Basf Ag | Process for the preparation of a solid herbicidal formulation |
-
2001
- 2001-07-21 DE DE10135641A patent/DE10135641A1/de not_active Withdrawn
-
2002
- 2002-07-12 PL PL02368678A patent/PL368678A1/xx not_active Application Discontinuation
- 2002-07-12 AU AU2002355175A patent/AU2002355175A1/en not_active Abandoned
- 2002-07-12 DE DE50208959T patent/DE50208959D1/de not_active Expired - Fee Related
- 2002-07-12 WO PCT/EP2002/007795 patent/WO2003009684A2/de active IP Right Grant
- 2002-07-12 HU HU0401489A patent/HUP0401489A3/hu unknown
- 2002-07-12 AT AT02751138T patent/ATE347806T1/de not_active IP Right Cessation
- 2002-07-12 RS YU34104A patent/RS34104A/sr unknown
- 2002-07-12 EA EA200400194A patent/EA007329B1/ru not_active IP Right Cessation
- 2002-07-12 EP EP02751138A patent/EP1418812B1/de not_active Expired - Lifetime
- 2002-07-18 US US10/198,310 patent/US20030050193A1/en not_active Abandoned
- 2002-12-07 UA UA2004021281A patent/UA78514C2/uk unknown
-
2004
- 2004-01-20 NO NO20040265A patent/NO20040265L/no not_active Application Discontinuation
- 2004-01-20 HR HR20040055A patent/HRP20040055A2/hr not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1418812B1 (de) | 2006-12-13 |
| WO2003009684A2 (de) | 2003-02-06 |
| WO2003009684A3 (de) | 2004-03-25 |
| AU2002355175A1 (en) | 2003-02-17 |
| EP1418812A2 (de) | 2004-05-19 |
| PL368678A1 (en) | 2005-04-04 |
| DE50208959D1 (de) | 2007-01-25 |
| US20030050193A1 (en) | 2003-03-13 |
| DE10135641A1 (de) | 2003-02-06 |
| ATE347806T1 (de) | 2007-01-15 |
| HUP0401489A2 (hu) | 2004-12-28 |
| EA007329B1 (ru) | 2006-08-25 |
| UA78514C2 (en) | 2007-04-10 |
| HUP0401489A3 (en) | 2005-11-28 |
| EA200400194A1 (ru) | 2004-06-24 |
| NO20040265L (no) | 2004-01-20 |
| RS34104A (en) | 2006-10-27 |
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| A1OB | Publication of a patent application | ||
| ARAI | Request for the grant of a patent on the basis of the submitted results of a substantive examination of a patent application | ||
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Owner name: BAYER CROPSCIENCE AG, DE |
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