CA2404353A1 - Synergistic herbicidal mixtures comprising a 6-phenoxypryid-2-ylcarboxamide - Google Patents
Synergistic herbicidal mixtures comprising a 6-phenoxypryid-2-ylcarboxamide Download PDFInfo
- Publication number
- CA2404353A1 CA2404353A1 CA002404353A CA2404353A CA2404353A1 CA 2404353 A1 CA2404353 A1 CA 2404353A1 CA 002404353 A CA002404353 A CA 002404353A CA 2404353 A CA2404353 A CA 2404353A CA 2404353 A1 CA2404353 A1 CA 2404353A1
- Authority
- CA
- Canada
- Prior art keywords
- ethyl
- cinidon
- picolinafen
- ylcarboxamide
- herbicidal compound
- Prior art date
- 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.)
- Abandoned
Links
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- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
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- 235000013877 carbamide Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
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- 238000011278 co-treatment Methods 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000007931 coated granule Substances 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000002301 combined effect Effects 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohex-2-enone Chemical compound O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 230000001419 dependent effect Effects 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
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical group CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 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
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 235000012245 magnesium oxide Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- PZYDAVFRVJXFHS-UHFFFAOYSA-N n-cyclohexyl-2-pyrrolidone Chemical compound O=C1CCCN1C1CCCCC1 PZYDAVFRVJXFHS-UHFFFAOYSA-N 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000010773 plant oil Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 238000004062 sedimentation Methods 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
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000005415 substituted alkoxy group Chemical group 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 210000003371 toe Anatomy 0.000 description 1
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 description 1
- 125000004950 trifluoroalkyl group Chemical group 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
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)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002654705A CA2654705A1 (en) | 2000-04-04 | 2001-04-04 | Synergistic herbicidal mixtures comprising a 6-phenoxypyrid-2-ylcarboxamide |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US19438300P | 2000-04-04 | 2000-04-04 | |
| US60/194,383 | 2000-04-04 | ||
| US23163100P | 2000-09-11 | 2000-09-11 | |
| US60/231,631 | 2000-09-11 | ||
| PCT/EP2001/003833 WO2001074157A2 (en) | 2000-04-04 | 2001-04-04 | Synergistic herbicidal mixtures |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002654705A Division CA2654705A1 (en) | 2000-04-04 | 2001-04-04 | Synergistic herbicidal mixtures comprising a 6-phenoxypyrid-2-ylcarboxamide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2404353A1 true CA2404353A1 (en) | 2001-10-11 |
Family
ID=26889956
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002404353A Abandoned CA2404353A1 (en) | 2000-04-04 | 2001-04-04 | Synergistic herbicidal mixtures comprising a 6-phenoxypryid-2-ylcarboxamide |
| CA002654705A Abandoned CA2654705A1 (en) | 2000-04-04 | 2001-04-04 | Synergistic herbicidal mixtures comprising a 6-phenoxypyrid-2-ylcarboxamide |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002654705A Abandoned CA2654705A1 (en) | 2000-04-04 | 2001-04-04 | Synergistic herbicidal mixtures comprising a 6-phenoxypyrid-2-ylcarboxamide |
Country Status (30)
| Country | Link |
|---|---|
| US (1) | US6645911B2 (enExample) |
| EP (2) | EP1267612B1 (enExample) |
| JP (1) | JP4749647B2 (enExample) |
| KR (2) | KR100736312B1 (enExample) |
| CN (2) | CN1679396A (enExample) |
| AT (2) | ATE336895T1 (enExample) |
| AU (3) | AU2001265857B2 (enExample) |
| BG (2) | BG65872B1 (enExample) |
| BR (1) | BR0109821A (enExample) |
| CA (2) | CA2404353A1 (enExample) |
| CZ (1) | CZ20023303A3 (enExample) |
| DE (2) | DE60106885T2 (enExample) |
| DK (2) | DK1267612T3 (enExample) |
| EA (2) | EA005763B1 (enExample) |
| ES (2) | ES2231509T3 (enExample) |
| GE (1) | GEP20063846B (enExample) |
| HR (2) | HRP20080308B1 (enExample) |
| HU (1) | HUP0300564A3 (enExample) |
| IL (1) | IL151816A (enExample) |
| IN (1) | IN2002CH01751A (enExample) |
| MX (1) | MXPA02009480A (enExample) |
| NZ (1) | NZ521599A (enExample) |
| PL (3) | PL204904B1 (enExample) |
| PT (1) | PT1267612E (enExample) |
| RS (3) | RS20090499A (enExample) |
| SI (1) | SI1464223T1 (enExample) |
| SK (1) | SK287815B6 (enExample) |
| UA (1) | UA75355C2 (enExample) |
| WO (1) | WO2001074157A2 (enExample) |
| ZA (1) | ZA200208902B (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU775959B2 (en) * | 1999-11-17 | 2004-08-19 | Bayer Cropscience Ag | Selective herbicides based upon 2,6-disubstituted pyridine derivatives |
| DE10160139A1 (de) * | 2001-12-07 | 2003-06-18 | Bayer Cropscience Gmbh | Synergistische herbizide Mittel enthaltend bestimmte Herbizide aus der Gruppe der Benzoylcylohexandione |
| US20060166827A1 (en) * | 2002-08-08 | 2006-07-27 | Kotzian Georg R | Herbicidal composition |
| MXPA05009186A (es) * | 2003-03-13 | 2005-10-18 | Basf Ag | Mezclas herbicidas que actuan sinergicamente. |
| ES2387618T3 (es) * | 2003-03-13 | 2012-09-27 | Basf Se | Mezclas herbicidas que contienen picolinafeno |
| WO2006006569A1 (ja) * | 2004-07-12 | 2006-01-19 | Nihon Nohyaku Co., Ltd. | フェニルピリジン類又はその塩類、これらを有効成分とする除草剤及びその使用方法 |
| KR20150052330A (ko) | 2007-09-24 | 2015-05-13 | 애플 인크. | 전자 장치 내의 내장형 인증 시스템들 |
| JP5563773B2 (ja) * | 2008-12-17 | 2014-07-30 | バイエル・クロップサイエンス・アーゲー | 除草剤組成物 |
| AR093955A1 (es) * | 2012-12-18 | 2015-07-01 | Bayer Cropscience Ag | Agentes herbicidas que contienen aclonifeno |
| EP2875727A1 (en) * | 2013-11-26 | 2015-05-27 | Basf Se | Aqueous suspension concentrates containing picolinafen |
| EP3079471A1 (de) * | 2013-12-11 | 2016-10-19 | Bayer CropScience Aktiengesellschaft | Herbizide mittel enthaltend flufenacet, picolinafen und metribuzin |
| WO2015086603A1 (de) * | 2013-12-11 | 2015-06-18 | Bayer Cropscience Ag | Herbizide mittel enthaltend flufenacet, picolinafen und pendimethalin |
| IL277679B2 (en) * | 2018-04-13 | 2024-06-01 | Bayer Ag | Solid formulation of insecticidal mixtures |
| CN113180037B (zh) * | 2020-01-14 | 2024-02-02 | 东莞市东阳光菌阳氢专利农药有限公司 | 一种环保型氟苯醚酰胺乳油制剂及其制备方法和用途 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3603789A1 (de) | 1986-02-07 | 1987-08-13 | Basf Ag | N-substituierte 3,4,5,6-tetrahydrophthalimide |
| US5237089A (en) | 1986-02-07 | 1993-08-17 | Basf Aktiengesellschaft | Nitro or amino substituted phenylalkyl or phenylalkenyl carboxylic acid derivatives |
| DE3821600A1 (de) * | 1988-06-27 | 1989-12-28 | Bayer Ag | Heteroaryloxyessigsaeure-n-isopropylanilide |
| GB9005965D0 (en) * | 1990-03-16 | 1990-05-09 | Shell Int Research | Herbicidal carboxamide derivatives |
| CN1074646C (zh) * | 1992-10-06 | 2001-11-14 | 国际壳牌研究有限公司 | 除草剂混合物 |
| DE19534910A1 (de) | 1995-09-20 | 1997-03-27 | Basf Ag | Herbizide Mischungen mit synergistischer Wirkung |
| US5859920A (en) * | 1995-11-30 | 1999-01-12 | Eastman Kodak Company | Method for embedding digital information in an image |
| DE19633271A1 (de) * | 1996-08-19 | 1998-02-26 | Basf Ag | Flüssige Formulierung von Ethyl-(Z)-2-chlor-3-[2-chlor-5-(4,5,6,7-tetrahydro-1,3-dioxoisoindoldion-2-yl)phenyl]acrylat |
| US6030924A (en) * | 1997-05-07 | 2000-02-29 | American Cyanamid Company | Solid formulations |
| JPH11116408A (ja) * | 1997-10-07 | 1999-04-27 | Sumitomo Chem Co Ltd | 除草剤組成物 |
| US5985796A (en) * | 1998-01-22 | 1999-11-16 | American Cyanamid Company | Herbicidal mixtures |
| JP2000038307A (ja) * | 1998-07-23 | 2000-02-08 | Sumitomo Chem Co Ltd | 除草剤組成物 |
| AU8561398A (en) * | 1998-08-07 | 2000-02-28 | Sumitomo Chemical Company, Limited | Herbicidal composition |
| HRP20010104B1 (hr) * | 1998-08-13 | 2011-01-31 | Bayer Cropscience Ag | Herbicidi s aciliranom aminofenilsulfonil ureom |
| DE19836700A1 (de) * | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Getreidekulturen |
| CZ20021141A3 (cs) * | 1999-09-30 | 2002-06-12 | Bayer Aktiengesellschaft | Selektivní herbicidy na bázi N-aryl-triazolin(thi)onů a jejich pouľití |
| US6252336B1 (en) * | 1999-11-08 | 2001-06-26 | Cts Corporation | Combined piezoelectric silent alarm/battery charger |
| AU775959B2 (en) | 1999-11-17 | 2004-08-19 | Bayer Cropscience Ag | Selective herbicides based upon 2,6-disubstituted pyridine derivatives |
-
2001
- 2001-04-04 ES ES01943220T patent/ES2231509T3/es not_active Expired - Lifetime
- 2001-04-04 EA EA200201051A patent/EA005763B1/ru not_active IP Right Cessation
- 2001-04-04 CN CNA2005100694761A patent/CN1679396A/zh active Pending
- 2001-04-04 DK DK01943220T patent/DK1267612T3/da active
- 2001-04-04 HR HRP20080308AA patent/HRP20080308B1/hr not_active IP Right Cessation
- 2001-04-04 HR HR20020867A patent/HRP20020867B1/xx not_active IP Right Cessation
- 2001-04-04 IL IL151816A patent/IL151816A/en active IP Right Grant
- 2001-04-04 GE GE4971A patent/GEP20063846B/en unknown
- 2001-04-04 PT PT01943220T patent/PT1267612E/pt unknown
- 2001-04-04 SK SK1425-2002A patent/SK287815B6/sk not_active IP Right Cessation
- 2001-04-04 CN CNB018074944A patent/CN1220433C/zh not_active Expired - Fee Related
- 2001-04-04 HU HU0300564A patent/HUP0300564A3/hu unknown
- 2001-04-04 CA CA002404353A patent/CA2404353A1/en not_active Abandoned
- 2001-04-04 BR BR0109821-7A patent/BR0109821A/pt not_active Application Discontinuation
- 2001-04-04 WO PCT/EP2001/003833 patent/WO2001074157A2/en not_active Ceased
- 2001-04-04 PL PL384851A patent/PL204904B1/pl not_active IP Right Cessation
- 2001-04-04 AT AT04016188T patent/ATE336895T1/de not_active IP Right Cessation
- 2001-04-04 RS RSP-2009/0499A patent/RS20090499A/sr unknown
- 2001-04-04 NZ NZ521599A patent/NZ521599A/en not_active IP Right Cessation
- 2001-04-04 RS RSP-2009/0500A patent/RS20090500A/sr unknown
- 2001-04-04 DK DK04016188T patent/DK1464223T3/da active
- 2001-04-04 EP EP01943220A patent/EP1267612B1/en not_active Expired - Lifetime
- 2001-04-04 MX MXPA02009480A patent/MXPA02009480A/es active IP Right Grant
- 2001-04-04 EP EP04016188A patent/EP1464223B1/en not_active Expired - Lifetime
- 2001-04-04 AU AU2001265857A patent/AU2001265857B2/en not_active Ceased
- 2001-04-04 PL PL384852A patent/PL204905B1/pl not_active IP Right Cessation
- 2001-04-04 CA CA002654705A patent/CA2654705A1/en not_active Abandoned
- 2001-04-04 ES ES04016188T patent/ES2271742T3/es not_active Expired - Lifetime
- 2001-04-04 RS YU73602A patent/RS51691B/sr unknown
- 2001-04-04 US US09/825,694 patent/US6645911B2/en not_active Expired - Fee Related
- 2001-04-04 AU AU6585701D patent/AU6585701A/xx active Pending
- 2001-04-04 UA UA2002118717A patent/UA75355C2/uk unknown
- 2001-04-04 KR KR1020077009449A patent/KR100736312B1/ko not_active Expired - Fee Related
- 2001-04-04 DE DE60106885T patent/DE60106885T2/de not_active Expired - Fee Related
- 2001-04-04 PL PL360851A patent/PL204929B1/pl unknown
- 2001-04-04 AT AT01943220T patent/ATE281073T1/de not_active IP Right Cessation
- 2001-04-04 JP JP2001571921A patent/JP4749647B2/ja not_active Expired - Fee Related
- 2001-04-04 DE DE60122600T patent/DE60122600T2/de not_active Expired - Fee Related
- 2001-04-04 CZ CZ20023303A patent/CZ20023303A3/cs unknown
- 2001-04-04 EA EA200400926A patent/EA006848B1/ru not_active IP Right Cessation
- 2001-04-04 SI SI200130610T patent/SI1464223T1/sl unknown
- 2001-04-04 KR KR1020027013215A patent/KR100732095B1/ko not_active Expired - Fee Related
-
2002
- 2002-09-30 BG BG107158A patent/BG65872B1/bg unknown
- 2002-10-24 IN IN1751CH2002 patent/IN2002CH01751A/en unknown
- 2002-11-01 ZA ZA200208902A patent/ZA200208902B/en unknown
-
2007
- 2007-01-25 AU AU2007200321A patent/AU2007200321B2/en not_active Ceased
-
2009
- 2009-09-02 BG BG10110457A patent/BG110457A/bg unknown
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| AU2001265857A1 (en) | Synergistic herbicidal mixtures |
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