http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PL-211732-B1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_981a37900e6991fb373304ed2ba5a703 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N41-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N35-06 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P13-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N41-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-36 |
| filingDate | 2002-11-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ec30a33afc3ea9f649179985418aefe http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b678f68916ff42aa5ff1cefdce5628ca http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e275063bf46ec7e47eb7950eda861899 |
| publicationDate | 2012-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | PL-211732-B1 |
| titleOfInvention | Herbicide, method of controlling undesirable plant growth and use of the composition |
| abstract | A composition contains an active agent combination of: 2-(2-chloro-3-(2,2,2-trifluoroethoxymethyl)-4-methylsulfonyl-benzoyl)-cyclohexane-1,3-dione (I); and at least one of about 55 other specific herbicides, e.g. ethoxysulfuron, formasulfuron, atrazine, 2,4-D, dicamba, acetochlor, pendimethalin, diflufenican, glyphosate or glufosinate. A herbicidal composition contains an active agent combination of: (a) 2-(2-chloro-3-(2,2,2-trifluoroethoxymethyl)-4-methylsulfonyl-benzoyl)-cyclohexane-1,3-dione (I) or its salt; and (b) at least one other herbicide selected from: (i) the branched aminoacid biosynthesis inhibitors ethoxysulfuron, flumetsulam, halosulfuron, imazamox, imazapyr, imazaquin, imazethapyr, metosulam, nicosulfuron, primisulfuron, prosulfuron, rimsulfuron, thifensulfuron-methyl, triflusulfuron and foramsulfuron; (ii) the photosynthesis electron transport inhibitors ametryne, atrazine, bromoxynil, cyanazine, diuron, hexazinone, metribuzin, pyridate and terbuthylazine; (iii) the synthetic auxins 2,4-D, clopyralid, dicamba, diflufenzopyr and fluroxypyr; (iv) the fatty acid biosynthesis inhibitors butylate, EPTC and fenoxaprop-P-ethyl; (v) the mitosis inhibitors acetochlor, alachlor, dimethenamid, flufenacet, mefenacet, metolachlor, thenylchlor and S-metalochlor, (6) the protoporphyrinogen oxidase inhibitors fluthiacet-methyl and carfentrazone-ethyl; (vi) the hydroxyphenyl pyruvate dioxygenase inhibitors isoxaflutole, mesotrione, sulcotrione and 4-(4-trifluoromethyl-2-methylsulfonyl-benzoyl)-5-hydroxy-1-methyl-3-methylpyrazole; (vii) glyphosate; (viii) pendimethalin; (ix) trifluralin; (x) asulam; (xi) triaziflam; (xii) diflufenican; and (xiii) glufosinate-ammonium. The weight ratio of (A) to (B) is 1-2000:2000-1. An independent claim is also included for a method for controlling undesirable weed growth, involving applying the combination of (A) and (B) to at least part of the plants or to the plant growth area. ACTIVITY : Herbicide. In post-emergence tests, the herbicidal ratings against Galium aparine were 50 % for 75 g/ha of (I), 30 % for 200 g/ha of atrazine and 90 % (compared with a predicted value of 68 %) for a combination of 75 g/ha (Ia) and 200 g/ha atrazine. MECHANISM OF ACTION : Branched Aminoacid Biosynthesis Inhibitor; Photosynthesis Electron Transport Inhibitor; Fatty Acid Biosynthesis Inhibitor; Mitosis Inhibitor; Protoporphyrinogen Oxidase Inhibitor; Hydroxyphenyl Pyruvate Dioxygenase Inhibitor. |
| priorityDate | 2001-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 189.