JP2019518717A5 - - Google Patents
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- Publication number
- JP2019518717A5 JP2019518717A5 JP2018551392A JP2018551392A JP2019518717A5 JP 2019518717 A5 JP2019518717 A5 JP 2019518717A5 JP 2018551392 A JP2018551392 A JP 2018551392A JP 2018551392 A JP2018551392 A JP 2018551392A JP 2019518717 A5 JP2019518717 A5 JP 2019518717A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- salt
- lithium
- sulfonylurea
- ethyl
- 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.)
- Granted
Links
- 150000003839 salts Chemical class 0.000 claims description 70
- -1 etamethosulfuron Chemical compound 0.000 claims description 66
- 229940100389 Sulfonylurea Drugs 0.000 claims description 57
- VWGAYSCWLXQJBQ-UHFFFAOYSA-N methyl 4-iodo-2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoate Chemical group COC(=O)C1=CC=C(I)C=C1S(=O)(=O)NC(=O)NC1=NC(C)=NC(OC)=N1 VWGAYSCWLXQJBQ-UHFFFAOYSA-N 0.000 claims description 56
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims description 56
- 229910003002 lithium salt Inorganic materials 0.000 claims description 54
- 159000000002 lithium salts Chemical class 0.000 claims description 54
- 239000000203 mixture Substances 0.000 claims description 47
- 239000005584 Metsulfuron-methyl Substances 0.000 claims description 41
- RSMUVYRMZCOLBH-UHFFFAOYSA-N metsulfuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=NC(OC)=N1 RSMUVYRMZCOLBH-UHFFFAOYSA-N 0.000 claims description 41
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 claims description 38
- 239000005472 Bensulfuron methyl Substances 0.000 claims description 30
- XMQFTWRPUQYINF-UHFFFAOYSA-N bensulfuron-methyl Chemical group COC(=O)C1=CC=CC=C1CS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 XMQFTWRPUQYINF-UHFFFAOYSA-N 0.000 claims description 30
- 230000002363 herbicidal effect Effects 0.000 claims description 29
- 239000005586 Nicosulfuron Substances 0.000 claims description 28
- RTCOGUMHFFWOJV-UHFFFAOYSA-N nicosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(=O)N(C)C)=N1 RTCOGUMHFFWOJV-UHFFFAOYSA-N 0.000 claims description 28
- 239000004009 herbicide Substances 0.000 claims description 19
- 239000005560 Foramsulfuron Substances 0.000 claims description 16
- NSWAMPCUPHPTTC-UHFFFAOYSA-N chlorimuron-ethyl Chemical group CCOC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(Cl)=CC(OC)=N1 NSWAMPCUPHPTTC-UHFFFAOYSA-N 0.000 claims description 16
- PXDNXJSDGQBLKS-UHFFFAOYSA-N foramsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(NC=O)C=2)C(=O)N(C)C)=N1 PXDNXJSDGQBLKS-UHFFFAOYSA-N 0.000 claims description 16
- BGNQYGRXEXDAIQ-UHFFFAOYSA-N Pyrazosulfuron-ethyl Chemical group C1=NN(C)C(S(=O)(=O)NC(=O)NC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OCC BGNQYGRXEXDAIQ-UHFFFAOYSA-N 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 13
- 239000005564 Halosulfuron methyl Substances 0.000 claims description 12
- FMGZEUWROYGLAY-UHFFFAOYSA-N Halosulfuron-methyl Chemical group ClC1=NN(C)C(S(=O)(=O)NC(=O)NC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OC FMGZEUWROYGLAY-UHFFFAOYSA-N 0.000 claims description 12
- 239000005616 Rimsulfuron Substances 0.000 claims description 12
- 239000005623 Thifensulfuron-methyl Substances 0.000 claims description 12
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 claims description 12
- MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 claims description 12
- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 claims description 12
- MAYMYMXYWIVVOK-UHFFFAOYSA-N 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-4-(methanesulfonamidomethyl)benzoic acid Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(CNS(C)(=O)=O)C=2)C(O)=O)=N1 MAYMYMXYWIVVOK-UHFFFAOYSA-N 0.000 claims description 10
- 239000003666 Amidosulfuron Substances 0.000 claims description 10
- CTTHWASMBLQOFR-UHFFFAOYSA-N Amidosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)=N1 CTTHWASMBLQOFR-UHFFFAOYSA-N 0.000 claims description 10
- 239000005504 Dicamba Substances 0.000 claims description 10
- 239000005577 Mesosulfuron Substances 0.000 claims description 10
- 239000003125 aqueous solvent Substances 0.000 claims description 10
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims description 10
- BNYHRGTXRPWASY-UHFFFAOYSA-N nonylsulfonylurea Chemical compound CCCCCCCCCS(=O)(=O)NC(N)=O BNYHRGTXRPWASY-UHFFFAOYSA-N 0.000 claims description 10
- VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 claims description 8
- 239000005496 Chlorsulfuron Substances 0.000 claims description 8
- VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 claims description 8
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- 239000011734 sodium Substances 0.000 claims description 7
- VQHHIQJPQOLZGF-UHFFFAOYSA-N 1-(2-iodophenyl)sulfonyl-3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)I)=N1 VQHHIQJPQOLZGF-UHFFFAOYSA-N 0.000 claims description 6
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 6
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 claims description 6
- 239000005492 Carfentrazone-ethyl Substances 0.000 claims description 6
- 239000005500 Clopyralid Substances 0.000 claims description 6
- 239000005507 Diflufenican Substances 0.000 claims description 6
- 239000005532 Flumioxazine Substances 0.000 claims description 6
- 239000005558 Fluroxypyr Substances 0.000 claims description 6
- 239000005562 Glyphosate Substances 0.000 claims description 6
- 239000005578 Mesotrione Substances 0.000 claims description 6
- YLPGTOIOYRQOHV-UHFFFAOYSA-N Pretilachlor Chemical compound CCCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC YLPGTOIOYRQOHV-UHFFFAOYSA-N 0.000 claims description 6
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- WYEHFWKAOXOVJD-UHFFFAOYSA-N diflufenican Chemical compound FC1=CC(F)=CC=C1NC(=O)C1=CC=CN=C1OC1=CC=CC(C(F)(F)F)=C1 WYEHFWKAOXOVJD-UHFFFAOYSA-N 0.000 claims description 6
- 239000006185 dispersion Substances 0.000 claims description 6
- MLKCGVHIFJBRCD-UHFFFAOYSA-N ethyl 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoate Chemical group C1=C(Cl)C(CC(Cl)C(=O)OCC)=CC(N2C(N(C(F)F)C(C)=N2)=O)=C1F MLKCGVHIFJBRCD-UHFFFAOYSA-N 0.000 claims description 6
- FOUWCSDKDDHKQP-UHFFFAOYSA-N flumioxazin Chemical compound FC1=CC=2OCC(=O)N(CC#C)C=2C=C1N(C1=O)C(=O)C2=C1CCCC2 FOUWCSDKDDHKQP-UHFFFAOYSA-N 0.000 claims description 6
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 claims description 6
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 claims description 6
- 229940031993 lithium benzoate Drugs 0.000 claims description 6
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 claims description 6
- 229910052808 lithium carbonate Inorganic materials 0.000 claims description 6
- 229940071264 lithium citrate Drugs 0.000 claims description 6
- WJSIUCDMWSDDCE-UHFFFAOYSA-K lithium citrate (anhydrous) Chemical compound [Li+].[Li+].[Li+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O WJSIUCDMWSDDCE-UHFFFAOYSA-K 0.000 claims description 6
- LDJNSLOKTFFLSL-UHFFFAOYSA-M lithium;benzoate Chemical compound [Li+].[O-]C(=O)C1=CC=CC=C1 LDJNSLOKTFFLSL-UHFFFAOYSA-M 0.000 claims description 6
- XKPJKVVZOOEMPK-UHFFFAOYSA-M lithium;formate Chemical compound [Li+].[O-]C=O XKPJKVVZOOEMPK-UHFFFAOYSA-M 0.000 claims description 6
- BTAUEIDLAAYHSL-UHFFFAOYSA-M lithium;octanoate Chemical compound [Li+].CCCCCCCC([O-])=O BTAUEIDLAAYHSL-UHFFFAOYSA-M 0.000 claims description 6
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 claims description 6
- WNTGYJSOUMFZEP-SSDOTTSWSA-N (R)-mecoprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-SSDOTTSWSA-N 0.000 claims description 4
- 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 description 4
- 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 description 4
- CLQMBPJKHLGMQK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)nicotinic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=CC=C1C(O)=O CLQMBPJKHLGMQK-UHFFFAOYSA-N 0.000 claims description 4
- IRJQWZWMQCVOLA-ZBKNUEDVSA-N 2-[(z)-n-[(3,5-difluorophenyl)carbamoylamino]-c-methylcarbonimidoyl]pyridine-3-carboxylic acid Chemical compound N=1C=CC=C(C(O)=O)C=1C(/C)=N\NC(=O)NC1=CC(F)=CC(F)=C1 IRJQWZWMQCVOLA-ZBKNUEDVSA-N 0.000 claims description 4
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 claims description 4
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 claims description 4
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 claims description 4
- MBFHUWCOCCICOK-UHFFFAOYSA-N 4-iodo-2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical group COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(I)C=2)C(O)=O)=N1 MBFHUWCOCCICOK-UHFFFAOYSA-N 0.000 claims description 4
- 239000005489 Bromoxynil Substances 0.000 claims description 4
- XVOKUMIPKHGGTN-UHFFFAOYSA-N Imazethapyr Chemical compound OC(=O)C1=CC(CC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 XVOKUMIPKHGGTN-UHFFFAOYSA-N 0.000 claims description 4
- 239000005568 Iodosulfuron Substances 0.000 claims description 4
- 239000005574 MCPA Substances 0.000 claims description 4
- 239000005575 MCPB Substances 0.000 claims description 4
- 101150039283 MCPB gene Proteins 0.000 claims description 4
- 239000005576 Mecoprop-P Substances 0.000 claims description 4
- 239000005601 Propoxycarbazone Substances 0.000 claims description 4
- 239000005604 Prosulfuron Substances 0.000 claims description 4
- LTUNNEGNEKBSEH-UHFFFAOYSA-N Prosulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)CCC(F)(F)F)=N1 LTUNNEGNEKBSEH-UHFFFAOYSA-N 0.000 claims description 4
- 239000005605 Pyraflufen-ethyl Substances 0.000 claims description 4
- 239000005619 Sulfosulfuron Substances 0.000 claims description 4
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims description 4
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 claims description 4
- 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 description 4
- HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 claims description 4
- PNCNFDRSHBFIDM-WOJGMQOQSA-N chembl111617 Chemical compound C=CCO\N=C(/CCC)C1=C(O)C(C(=O)OC)C(C)(C)CC1=O PNCNFDRSHBFIDM-WOJGMQOQSA-N 0.000 claims description 4
- MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 claims description 4
- PQKBPHSEKWERTG-LLVKDONJSA-N ethyl (2r)-2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoate Chemical group C1=CC(O[C@H](C)C(=O)OCC)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 PQKBPHSEKWERTG-LLVKDONJSA-N 0.000 claims description 4
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 4
- 229940097068 glyphosate Drugs 0.000 claims description 4
- MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical group C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 claims description 4
- INHCSSUBVCNVSK-UHFFFAOYSA-L lithium sulfate Inorganic materials [Li+].[Li+].[O-]S([O-])(=O)=O INHCSSUBVCNVSK-UHFFFAOYSA-L 0.000 claims description 4
- XIGAUIHYSDTJHW-UHFFFAOYSA-N mefenacet Chemical compound N=1C2=CC=CC=C2SC=1OCC(=O)N(C)C1=CC=CC=C1 XIGAUIHYSDTJHW-UHFFFAOYSA-N 0.000 claims description 4
- 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 description 4
- 229960002939 metizoline Drugs 0.000 claims description 4
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 claims description 4
- JZPKLLLUDLHCEL-UHFFFAOYSA-N pentoxazone Chemical compound O=C1C(=C(C)C)OC(=O)N1C1=CC(OC2CCCC2)=C(Cl)C=C1F JZPKLLLUDLHCEL-UHFFFAOYSA-N 0.000 claims description 4
- LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 claims description 4
- APTZNLHMIGJTEW-UHFFFAOYSA-N pyraflufen-ethyl Chemical group C1=C(Cl)C(OCC(=O)OCC)=CC(C=2C(=C(OC(F)F)N(C)N=2)Cl)=C1F APTZNLHMIGJTEW-UHFFFAOYSA-N 0.000 claims description 4
- USSIUIGPBLPCDF-KEBDBYFISA-N pyriminobac-methyl Chemical group CO\N=C(/C)C1=CC=CC(OC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OC USSIUIGPBLPCDF-KEBDBYFISA-N 0.000 claims description 4
- FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 claims description 4
- RBTVSNLYYIMMKS-UHFFFAOYSA-N tert-butyl 3-aminoazetidine-1-carboxylate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)N1CC(N)C1 RBTVSNLYYIMMKS-UHFFFAOYSA-N 0.000 claims description 4
- XSKZXGDFSCCXQX-UHFFFAOYSA-N thiencarbazone-methyl Chemical compound COC(=O)C1=CSC(C)=C1S(=O)(=O)NC(=O)N1C(=O)N(C)C(OC)=N1 XSKZXGDFSCCXQX-UHFFFAOYSA-N 0.000 claims description 4
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 claims description 4
- 239000005468 Aminopyralid Substances 0.000 claims description 3
- NNYRZQHKCHEXSD-UHFFFAOYSA-N Daimuron Chemical compound C1=CC(C)=CC=C1NC(=O)NC(C)(C)C1=CC=CC=C1 NNYRZQHKCHEXSD-UHFFFAOYSA-N 0.000 claims description 3
- LLQPHQFNMLZJMP-UHFFFAOYSA-N Fentrazamide Chemical compound N1=NN(C=2C(=CC=CC=2)Cl)C(=O)N1C(=O)N(CC)C1CCCCC1 LLQPHQFNMLZJMP-UHFFFAOYSA-N 0.000 claims description 3
- 239000005529 Florasulam Substances 0.000 claims description 3
- QZXATCCPQKOEIH-UHFFFAOYSA-N Florasulam Chemical compound N=1N2C(OC)=NC=C(F)C2=NC=1S(=O)(=O)NC1=C(F)C=CC=C1F QZXATCCPQKOEIH-UHFFFAOYSA-N 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- NIXXQNOQHKNPEJ-UHFFFAOYSA-N aminopyralid Chemical compound NC1=CC(Cl)=NC(C(O)=O)=C1Cl NIXXQNOQHKNPEJ-UHFFFAOYSA-N 0.000 claims description 3
- WZDDLAZXUYIVMU-UHFFFAOYSA-N bromobutide Chemical compound CC(C)(C)C(Br)C(=O)NC(C)(C)C1=CC=CC=C1 WZDDLAZXUYIVMU-UHFFFAOYSA-N 0.000 claims description 3
- 229910017053 inorganic salt Inorganic materials 0.000 claims description 3
- 229910001386 lithium phosphate Inorganic materials 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 229910001463 metal phosphate Inorganic materials 0.000 claims description 3
- TWQULNDIKKJZPH-UHFFFAOYSA-K trilithium;phosphate Chemical group [Li+].[Li+].[Li+].[O-]P([O-])([O-])=O TWQULNDIKKJZPH-UHFFFAOYSA-K 0.000 claims description 3
- VIXCLRUCUMWJFF-KGLIPLIRSA-N (1R,5S)-benzobicyclon Chemical compound CS(=O)(=O)c1ccc(C(=O)C2=C(Sc3ccccc3)[C@H]3CC[C@H](C3)C2=O)c(Cl)c1 VIXCLRUCUMWJFF-KGLIPLIRSA-N 0.000 claims description 2
- IPPAUTOBDWNELX-UHFFFAOYSA-N (2-ethoxy-2-oxoethyl) 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate Chemical group C1=C([N+]([O-])=O)C(C(=O)OCC(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 IPPAUTOBDWNELX-UHFFFAOYSA-N 0.000 claims description 2
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Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP16175549.1 | 2016-06-21 | ||
| EP16175549 | 2016-06-21 | ||
| EP17156451 | 2017-02-16 | ||
| EP17156451.1 | 2017-02-16 | ||
| PCT/EP2017/065289 WO2017220680A1 (en) | 2016-06-21 | 2017-06-21 | Liquid sulfonylurea- and li-salt containing herbicidal compositions |
Publications (4)
| Publication Number | Publication Date |
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| JP2019518717A JP2019518717A (ja) | 2019-07-04 |
| JP2019518717A5 true JP2019518717A5 (enExample) | 2020-02-06 |
| JP6811784B2 JP6811784B2 (ja) | 2021-01-13 |
| JP6811784B6 JP6811784B6 (ja) | 2023-03-22 |
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Family Applications (1)
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| JP2018551392A Active JP6811784B6 (ja) | 2016-06-21 | 2017-06-21 | 液体スルホニル尿素およびＬｉ塩を含有する除草組成物 |
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| US (2) | US11464225B2 (enExample) |
| EP (2) | EP3549443A1 (enExample) |
| JP (1) | JP6811784B6 (enExample) |
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| ES (1) | ES2732049T3 (enExample) |
| HU (1) | HUE043981T2 (enExample) |
| LT (1) | LT3416486T (enExample) |
| MX (1) | MX372576B (enExample) |
| MY (1) | MY198487A (enExample) |
| PL (1) | PL3416486T3 (enExample) |
| PT (1) | PT3416486T (enExample) |
| RS (1) | RS58885B1 (enExample) |
| UA (1) | UA120736C2 (enExample) |
| WO (1) | WO2017220680A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11071296B2 (en) | 2014-12-22 | 2021-07-27 | Mitsui Agriscience International S.A./N.V. | Liquid sulfonylurea-containing herbicidal compositions |
| ES2732049T3 (es) * | 2016-06-21 | 2019-11-20 | Battelle Uk Ltd | Composiciones herbicidas que contienen sal de Li y sulfonilurea líquida |
| US11109588B2 (en) | 2019-02-19 | 2021-09-07 | Gowan Company, L.L.C. | Stable liquid formulations and methods of using the same |
| JP2022521281A (ja) * | 2019-02-25 | 2022-04-06 | クラリアント・インターナシヨナル・リミテツド | 相乗的な除草剤の組み合わせ |
| WO2020234175A1 (en) | 2019-05-21 | 2020-11-26 | Syngenta Crop Protection Ag | Improved herbicidal oil dispersion compositions |
| EP4096400A1 (en) * | 2020-01-29 | 2022-12-07 | FMC Agricultural Caribe Industries Ltd. | Liquid sulfonylurea compositions |
| EP3900535A1 (en) * | 2020-04-24 | 2021-10-27 | Battelle UK Limited | Liquid sulfonylurea herbicide composition |
| MX2023002402A (es) * | 2020-08-27 | 2023-05-09 | Contact Organics Tech Pty Ltd | Composicion herbicida con base en acido graso. |
| RU2767999C1 (ru) * | 2021-08-05 | 2022-03-22 | ООО "Агро Эксперт Груп" | Жидкая гербицидная композиция |
| PL445702A1 (pl) * | 2023-07-28 | 2025-02-03 | Pestila Spółka Z Ograniczoną Odpowiedzialnością | Kompozycja herbicydu oraz sposób jej wytwarzania |
| GB202312744D0 (en) * | 2023-08-21 | 2023-10-04 | Upl Mauritius Ltd | Herbicide safener composition |
Family Cites Families (67)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA915702A (en) | 1970-05-21 | 1972-11-28 | Eric Lucien | Preparation of 1-benzene-sulfonyl-3-hydrocarbylureas and derivatives |
| GB2059773B (en) | 1979-10-12 | 1983-01-12 | Boots Co Ltd | Fungicidal compositions |
| MA19709A1 (fr) | 1982-02-17 | 1983-10-01 | Ciba Geigy Ag | Application de derives de quinoleine a la protection des plantes cultivees . |
| EP0094349B1 (de) | 1982-05-07 | 1994-04-06 | Ciba-Geigy Ag | Verwendung von Chinolinderivaten zum Schützen von Kulturpflanzen |
| US4579583A (en) | 1982-09-08 | 1986-04-01 | Ciba-Geigy Corporation | Novel sulfonylureas |
| EP0138938A1 (en) | 1983-03-31 | 1985-05-02 | Robert Edward Silman | Method and device for detecting microorganisms |
| JPS59205305A (ja) * | 1983-04-04 | 1984-11-20 | イ−・アイ・デユポン・デ・ニモアス・アンド・カンパニ− | スルホニル尿素類の農業用安定化水性組成物 |
| EP0124295B1 (en) * | 1983-04-04 | 1991-04-03 | E.I. Du Pont De Nemours And Company | Stabilized aqueous formulations of sulfonylureas |
| US4936900A (en) * | 1983-04-04 | 1990-06-26 | E. I. Du Pont De Nemours And Company | Stabilized aqueous formulations of sulfonylurea salts |
| JPS6087254A (ja) | 1983-10-19 | 1985-05-16 | Japan Carlit Co Ltd:The | 新規尿素化合物及びそれを含有する除草剤 |
| US4599412A (en) * | 1983-11-23 | 1986-07-08 | E. I. Du Pont De Nemours And Company | Process for preparation of sulfonylurea solution formulations |
| DE3525205A1 (de) | 1984-09-11 | 1986-03-20 | Hoechst Ag, 6230 Frankfurt | Pflanzenschuetzende mittel auf basis von 1,2,4-triazolderivaten sowie neue derivate des 1,2,4-triazols |
| EP0191736B1 (de) | 1985-02-14 | 1991-07-17 | Ciba-Geigy Ag | Verwendung von Chinolinderivaten zum Schützen von Kulturpflanzen |
| DE3633840A1 (de) | 1986-10-04 | 1988-04-14 | Hoechst Ag | Phenylpyrazolcarbonsaeurederivate, ihre herstellung und verwendung als pflanzenwachstumsregulatoren und safener |
| DE3808896A1 (de) | 1988-03-17 | 1989-09-28 | Hoechst Ag | Pflanzenschuetzende mittel auf basis von pyrazolcarbonsaeurederivaten |
| DE3817192A1 (de) | 1988-05-20 | 1989-11-30 | Hoechst Ag | 1,2,4-triazolderivate enthaltende pflanzenschuetzende mittel sowie neue derivate des 1,2,4-triazols |
| EP0493471A1 (en) | 1989-09-21 | 1992-07-08 | E.I. Du Pont De Nemours And Company | Stabilization of non-aqueous suspensions |
| DE3939010A1 (de) | 1989-11-25 | 1991-05-29 | Hoechst Ag | Isoxazoline, verfahren zu ihrer herstellung und ihre verwendung als pflanzenschuetzende mittel |
| DE3939503A1 (de) | 1989-11-30 | 1991-06-06 | Hoechst Ag | Neue pyrazoline zum schutz von kulturpflanzen gegenueber herbiziden |
| EP0492366B1 (de) | 1990-12-21 | 1997-03-26 | Hoechst Schering AgrEvo GmbH | Neue 5-Chlorchinolin-8-oxyalkancarbonsäurederivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Antidots von Herbiziden |
| CA2127093A1 (en) | 1992-01-06 | 1993-07-22 | David Allan Jackisch | Tablet formulation with internal desiccant |
| EP0554015B1 (en) | 1992-01-28 | 1995-03-22 | Ishihara Sangyo Kaisha, Ltd. | Chemically stabilized herbicidal oil-based suspension |
| AU3801793A (en) | 1992-05-12 | 1993-12-13 | Church & Dwight Company, Inc. | Herbicide compositions |
| TW259690B (enExample) | 1992-08-01 | 1995-10-11 | Hoechst Ag | |
| DE4331448A1 (de) | 1993-09-16 | 1995-03-23 | Hoechst Schering Agrevo Gmbh | Substituierte Isoxazoline, Verfahren zu deren Herstellung, diese enthaltende Mittel und deren Verwendung als Safener |
| US5707928A (en) | 1993-09-28 | 1998-01-13 | American Cyanamid Company | Emulsifiable suspension concentrate compositions of imidazolinyl benzoic acids, esters and salts thereof, and dinitroaniline herbicides |
| CA2176513C (en) | 1993-11-15 | 2004-04-13 | Herbert Benson Scher | Microcapsules containing suspensions of biologically active compounds |
| US5830827A (en) | 1995-09-21 | 1998-11-03 | Ishihara Sangyo Kaisha, Ltd. | Granular herbicidal composition comprising flazasulfuron and a sulfosuccinate or benzoate stabilizer |
| CN1159881A (zh) | 1996-03-14 | 1997-09-24 | 化学工业部沈阳化工研究院 | 磺酰脲类除草混剂 |
| US5731264A (en) | 1996-10-17 | 1998-03-24 | Isp Investments Inc. | Stabilized liquid emulsifiable concentrate for a sulfonyl or sulfamoylurea herbicide |
| CN1181880A (zh) | 1996-11-12 | 1998-05-20 | 湖南化工研究院 | 水稻秧田和直播田除草剂系列组合物 |
| EP0944322A1 (en) | 1996-11-22 | 1999-09-29 | E.I. Du Pont De Nemours And Company | Quarternary ammonium salts and their use in agricultural formulations |
| BRPI9807183B1 (pt) | 1997-02-05 | 2015-10-20 | Basf Ag | mistura sólida, e, processos para a preparação de formulações herbicidas |
| JP4189612B2 (ja) | 1998-09-24 | 2008-12-03 | 日産化学工業株式会社 | 安定化する懸濁除草製剤 |
| CN1157113C (zh) | 1999-01-07 | 2004-07-14 | 石原产业株式会社 | 水田用水面漂浮性农药组合物、其使用方法及其制造方法 |
| US6860617B2 (en) | 1999-10-01 | 2005-03-01 | Ole K. Nilssen | Compact luminaire |
| AR030412A1 (es) | 2000-03-22 | 2003-08-20 | Fmc Corp | Proceso novedoso para preparar formulaciones acuosas |
| TWI243019B (en) | 2000-08-31 | 2005-11-11 | Basf Ag | Process for the preparation of a solid herbicidal formulation |
| US6831041B2 (en) | 2000-09-13 | 2004-12-14 | Basf Aktiengesellschaft | Oil suspension concentrates based on a cyclohexenone oxime ether lithium salt and the use thereof as plant protection agents |
| AU2002250096A1 (en) | 2001-02-02 | 2002-08-19 | E. I. Du Pont De Nemours And Company | Method for controlling weeds in lettuce |
| US6740653B2 (en) | 2001-12-18 | 2004-05-25 | Isp Investments Inc. | Shelf life extension of microemulsions containing active aza biocide |
| AR041211A1 (es) | 2002-09-12 | 2005-05-11 | Du Pont | Procedimiento para preparar composiciones de sulfonamida extruidas en pasta |
| DE10334301A1 (de) * | 2003-07-28 | 2005-03-03 | Bayer Cropscience Gmbh | Flüssige Formulierung |
| ES2302038T3 (es) | 2003-11-03 | 2008-07-01 | Bayer Cropscience Ag | Agente activo como herbicida. |
| US20060031174A1 (en) | 2004-07-20 | 2006-02-09 | Scribocel, Inc. | Method of authentication and indentification for computerized and networked systems |
| JP4506550B2 (ja) | 2004-08-04 | 2010-07-21 | 株式会社デンソー | 金属接続方法 |
| NZ563883A (en) | 2005-06-04 | 2011-02-25 | Bayer Cropscience Ag | Oil suspension concentrate comprising dioxazine pyridylsulfonylureas |
| JP5137348B2 (ja) | 2005-08-10 | 2013-02-06 | 石原産業株式会社 | 水性懸濁状除草組成物 |
| ZA200802442B (en) | 2005-09-01 | 2010-02-24 | Du Pont | Liquid sulfonylurea herbicide formulations |
| KR101294781B1 (ko) | 2006-08-08 | 2013-08-09 | 엘지전자 주식회사 | 랜덤 액세스 프리앰블 전송 방법 |
| US8263530B2 (en) | 2006-11-23 | 2012-09-11 | Gat Microencapsulation Ag | Agrochemical formulations containing microcapsules |
| TW200843642A (en) * | 2007-03-08 | 2008-11-16 | Du Pont | Liquid sulfonylurea herbicide formulations |
| ES2323399B2 (es) | 2007-06-19 | 2010-02-26 | Gat Microencapsulation Ag | Suspensiones en aceites de sulfonilureas y combinaciones agroquimicas. |
| EP2326169B1 (en) | 2008-05-28 | 2016-07-27 | GAT Microencapsulation GmbH | Suspension concentrates in oil of sulfonylureas and combinations with fluroxypyr or other agrochemicals |
| US8973283B2 (en) | 2009-02-03 | 2015-03-10 | Praxair Technology, Inc. | System and method for solvent recovery in a batch fluidized bed process |
| US8962004B2 (en) | 2011-04-05 | 2015-02-24 | Arysta Lifescience North America, Llc | Encapsulated triazinyl sulfonylurea herbicide and methods of use |
| WO2012175899A1 (en) | 2011-06-23 | 2012-12-27 | Syngenta Limited | Herbicidal composition comprising a pyrandione herbicide and a sulfonyl urea herbicide |
| GB2496643B (en) | 2011-11-17 | 2016-08-17 | Rotam Agrochem Int Co Ltd | Herbicidal suspension concentrate |
| CN102592519B (zh) | 2011-11-18 | 2014-09-17 | 深圳市华星光电技术有限公司 | 平板显示装置以及立体显示装置 |
| WO2013145131A1 (ja) | 2012-03-27 | 2013-10-03 | 富士通株式会社 | 管理制御装置、情報処理システム及び管理制御方法 |
| CN103371160A (zh) | 2012-04-27 | 2013-10-30 | 龙灯农业化工国际有限公司 | 一种降低药物残留的农药组合物 |
| PT2854543T (pt) | 2012-05-25 | 2016-11-23 | Bayer Cropscience Ag | Estabilização química de sal de sódio de metil iodossulfurão por hidroxiestearatos |
| US8871681B2 (en) | 2012-07-24 | 2014-10-28 | Dow Agrosciences Llc | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and certain sulfonylureas |
| US8522314B1 (en) | 2012-07-24 | 2013-08-27 | Google Inc. | VoIP phone authentication |
| US11071296B2 (en) | 2014-12-22 | 2021-07-27 | Mitsui Agriscience International S.A./N.V. | Liquid sulfonylurea-containing herbicidal compositions |
| GB201603207D0 (en) | 2016-02-24 | 2016-04-06 | Cooper Technologies Co | Electronic device configuration |
| ES2732049T3 (es) * | 2016-06-21 | 2019-11-20 | Battelle Uk Ltd | Composiciones herbicidas que contienen sal de Li y sulfonilurea líquida |
-
2017
- 2017-06-21 ES ES17733415T patent/ES2732049T3/es active Active
- 2017-06-21 WO PCT/EP2017/065289 patent/WO2017220680A1/en not_active Ceased
- 2017-06-21 UA UAA201809618A patent/UA120736C2/uk unknown
- 2017-06-21 CA CA3018651A patent/CA3018651C/en active Active
- 2017-06-21 MY MYPI2018001608A patent/MY198487A/en unknown
- 2017-06-21 LT LTEP17733415.8T patent/LT3416486T/lt unknown
- 2017-06-21 MX MX2018012367A patent/MX372576B/es active IP Right Grant
- 2017-06-21 KR KR1020187029826A patent/KR102163883B1/ko active Active
- 2017-06-21 EA EA201891997A patent/EA033330B1/ru unknown
- 2017-06-21 CN CN201780024577.8A patent/CN110035657B/zh active Active
- 2017-06-21 EP EP19175100.7A patent/EP3549443A1/en not_active Withdrawn
- 2017-06-21 US US16/087,576 patent/US11464225B2/en active Active
- 2017-06-21 AU AU2017281579A patent/AU2017281579B2/en active Active
- 2017-06-21 RS RS20190768A patent/RS58885B1/sr unknown
- 2017-06-21 JP JP2018551392A patent/JP6811784B6/ja active Active
- 2017-06-21 PT PT17733415T patent/PT3416486T/pt unknown
- 2017-06-21 PL PL17733415T patent/PL3416486T3/pl unknown
- 2017-06-21 HU HUE17733415A patent/HUE043981T2/hu unknown
- 2017-06-21 EP EP17733415.8A patent/EP3416486B1/en active Active
-
2018
- 2018-10-19 CO CONC2018/0011196A patent/CO2018011196A2/es unknown
-
2022
- 2022-07-26 US US17/873,854 patent/US12364261B2/en active Active
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