MX2008012995A - Mezclas herbicidas. - Google Patents
Mezclas herbicidas.Info
- Publication number
- MX2008012995A MX2008012995A MX2008012995A MX2008012995A MX2008012995A MX 2008012995 A MX2008012995 A MX 2008012995A MX 2008012995 A MX2008012995 A MX 2008012995A MX 2008012995 A MX2008012995 A MX 2008012995A MX 2008012995 A MX2008012995 A MX 2008012995A
- Authority
- MX
- Mexico
- Prior art keywords
- compound
- methyl
- amino
- chloro
- inhibitors
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 252
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 159
- 150000001875 compounds Chemical class 0.000 claims abstract description 420
- 239000003112 inhibitor Substances 0.000 claims abstract description 70
- 239000004009 herbicide Substances 0.000 claims abstract description 64
- 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 abstract description 62
- GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 claims abstract description 36
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims abstract description 29
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims abstract description 29
- 238000000034 method Methods 0.000 claims abstract description 26
- OTSAMNSACVKIOJ-UHFFFAOYSA-N azane;carbamoyl(ethoxy)phosphinic acid Chemical compound [NH4+].CCOP([O-])(=O)C(N)=O OTSAMNSACVKIOJ-UHFFFAOYSA-N 0.000 claims abstract description 23
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims abstract description 23
- 239000005571 Isoxaflutole Substances 0.000 claims abstract description 22
- OYIKARCXOQLFHF-UHFFFAOYSA-N isoxaflutole Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(=O)C1=C(C2CC2)ON=C1 OYIKARCXOQLFHF-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229940088649 isoxaflutole Drugs 0.000 claims abstract description 22
- 150000003839 salts Chemical class 0.000 claims abstract description 22
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical class C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 claims abstract description 18
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 17
- 229930192334 Auxin Natural products 0.000 claims abstract description 16
- 239000002363 auxin Substances 0.000 claims abstract description 16
- 230000012010 growth Effects 0.000 claims abstract description 16
- 150000004669 very long chain fatty acids Chemical class 0.000 claims abstract description 15
- 108010060806 Photosystem II Protein Complex Proteins 0.000 claims abstract description 12
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract description 11
- 125000005081 alkoxyalkoxyalkyl group Chemical group 0.000 claims abstract description 11
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 10
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 10
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 claims abstract description 10
- 108010081996 Photosystem I Protein Complex Proteins 0.000 claims abstract description 8
- 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 claims abstract description 6
- 108010020183 3-phosphoshikimate 1-carboxyvinyltransferase Proteins 0.000 claims abstract description 6
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 claims abstract description 6
- GMBRUAIJEFRHFQ-UHFFFAOYSA-N Fenchlorazole-ethyl Chemical group N1=C(C(=O)OCC)N=C(C(Cl)(Cl)Cl)N1C1=CC=C(Cl)C=C1Cl GMBRUAIJEFRHFQ-UHFFFAOYSA-N 0.000 claims abstract description 6
- UKSLKNUCVPZQCQ-UHFFFAOYSA-N Fluxofenim Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)=NOCC1OCCO1 UKSLKNUCVPZQCQ-UHFFFAOYSA-N 0.000 claims abstract description 6
- BWPYBAJTDILQPY-UHFFFAOYSA-N Methoxyphenone Chemical compound C1=C(C)C(OC)=CC=C1C(=O)C1=CC=CC(C)=C1 BWPYBAJTDILQPY-UHFFFAOYSA-N 0.000 claims abstract description 6
- 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 claims abstract description 6
- COYBRKAVBMYYSF-UHFFFAOYSA-N heptan-2-yl [(5-chloroquinolin-8-yl)oxy]acetate Chemical group C1=CN=C2C(OCC(=O)OC(C)CCCCC)=CC=C(Cl)C2=C1 COYBRKAVBMYYSF-UHFFFAOYSA-N 0.000 claims abstract description 6
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims abstract description 5
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims abstract description 5
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000005644 Dazomet Substances 0.000 claims abstract description 5
- YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 claims abstract description 5
- LBGPXIPGGRQBJW-UHFFFAOYSA-N Difenzoquat Chemical compound C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 LBGPXIPGGRQBJW-UHFFFAOYSA-N 0.000 claims abstract description 5
- ICWUMLXQKFTJMH-UHFFFAOYSA-N Etobenzanid Chemical compound C1=CC(OCOCC)=CC=C1C(=O)NC1=CC=CC(Cl)=C1Cl ICWUMLXQKFTJMH-UHFFFAOYSA-N 0.000 claims abstract description 5
- GXAMYUGOODKVRM-UHFFFAOYSA-N Flurecol Chemical compound C1=CC=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 GXAMYUGOODKVRM-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000005642 Oleic acid Substances 0.000 claims abstract description 5
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000005643 Pelargonic acid Substances 0.000 claims abstract description 5
- 208000014347 autosomal dominant hyaline body myopathy Diseases 0.000 claims abstract description 5
- 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 abstract description 5
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 claims abstract description 5
- OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical group CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 claims abstract description 5
- SDIXRDNYIMOKSG-UHFFFAOYSA-L disodium methyl arsenate Chemical compound [Na+].[Na+].C[As]([O-])([O-])=O SDIXRDNYIMOKSG-UHFFFAOYSA-L 0.000 claims abstract description 5
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims abstract description 5
- RBNIGDFIUWJJEV-LLVKDONJSA-N methyl (2r)-2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N([C@H](C)C(=O)OC)C(=O)C1=CC=CC=C1 RBNIGDFIUWJJEV-LLVKDONJSA-N 0.000 claims abstract description 5
- JITOKQVGRJSHHA-UHFFFAOYSA-M monosodium methyl arsenate Chemical compound [Na+].C[As](O)([O-])=O JITOKQVGRJSHHA-UHFFFAOYSA-M 0.000 claims abstract description 5
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims abstract description 5
- IKVXBIIHQGXQRQ-CYBMUJFWSA-N propan-2-yl (2r)-2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N([C@H](C)C(=O)OC(C)C)C(=O)C1=CC=CC=C1 IKVXBIIHQGXQRQ-CYBMUJFWSA-N 0.000 claims abstract description 5
- 150000003230 pyrimidines Chemical class 0.000 claims abstract description 5
- XKTYXVDYIKIYJP-UHFFFAOYSA-N 3h-dioxole Chemical compound C1OOC=C1 XKTYXVDYIKIYJP-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000005499 Clomazone Substances 0.000 claims abstract description 4
- 239000002169 Metam Substances 0.000 claims abstract description 4
- VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 claims abstract description 4
- KIEDNEWSYUYDSN-UHFFFAOYSA-N clomazone Chemical compound O=C1C(C)(C)CON1CC1=CC=CC=C1Cl KIEDNEWSYUYDSN-UHFFFAOYSA-N 0.000 claims abstract description 4
- HYVVJDQGXFXBRZ-UHFFFAOYSA-N metam Chemical compound CNC(S)=S HYVVJDQGXFXBRZ-UHFFFAOYSA-N 0.000 claims abstract description 4
- -1 fosamin-ammonium Chemical compound 0.000 claims description 106
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 87
- 239000005562 Glyphosate Substances 0.000 claims description 76
- 229940097068 glyphosate Drugs 0.000 claims description 56
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 56
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 claims description 54
- 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 49
- 239000005560 Foramsulfuron Substances 0.000 claims description 47
- 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 47
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 39
- 239000005498 Clodinafop Substances 0.000 claims description 35
- YUIKUTLBPMDDNQ-MRVPVSSYSA-N clodinafop Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=NC=C(Cl)C=C1F YUIKUTLBPMDDNQ-MRVPVSSYSA-N 0.000 claims description 35
- 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 33
- MPPOHAUSNPTFAJ-UHFFFAOYSA-N 2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 MPPOHAUSNPTFAJ-UHFFFAOYSA-N 0.000 claims description 32
- 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 30
- 239000005561 Glufosinate Substances 0.000 claims description 30
- WVQBLGZPHOPPFO-LBPRGKRZSA-N (S)-metolachlor Chemical compound CCC1=CC=CC(C)=C1N([C@@H](C)COC)C(=O)CCl WVQBLGZPHOPPFO-LBPRGKRZSA-N 0.000 claims description 28
- 239000005617 S-Metolachlor Substances 0.000 claims description 28
- 239000005616 Rimsulfuron Substances 0.000 claims description 27
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 claims description 27
- 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 27
- 239000005586 Nicosulfuron Substances 0.000 claims description 26
- 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 26
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 claims description 24
- 239000005510 Diuron Substances 0.000 claims description 24
- 239000005558 Fluroxypyr Substances 0.000 claims description 20
- 239000005590 Oxyfluorfen Substances 0.000 claims description 20
- OQMBBFQZGJFLBU-UHFFFAOYSA-N Oxyfluorfen Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 OQMBBFQZGJFLBU-UHFFFAOYSA-N 0.000 claims description 20
- 239000005623 Thifensulfuron-methyl Substances 0.000 claims description 20
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 claims description 20
- 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 20
- 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 20
- YHKBGVDUSSWOAB-UHFFFAOYSA-N 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoic acid Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(CC(Cl)C(O)=O)=C(Cl)C=C1F YHKBGVDUSSWOAB-UHFFFAOYSA-N 0.000 claims description 19
- 239000005574 MCPA Substances 0.000 claims description 19
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims description 19
- 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 18
- 239000003085 diluting agent Substances 0.000 claims description 15
- 108010000700 Acetolactate synthase Proteins 0.000 claims description 13
- 239000004094 surface-active agent Substances 0.000 claims description 13
- 102000000452 Acetyl-CoA carboxylase Human genes 0.000 claims description 11
- 108010016219 Acetyl-CoA carboxylase Proteins 0.000 claims description 11
- 108020001991 Protoporphyrinogen Oxidase Proteins 0.000 claims description 10
- 102000005396 glutamine synthetase Human genes 0.000 claims description 10
- 108020002326 glutamine synthetase Proteins 0.000 claims description 10
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 10
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 9
- 102000005135 Protoporphyrinogen oxidase Human genes 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 8
- KWAIHLIXESXTJL-UHFFFAOYSA-N aminocyclopyrachlor Chemical compound OC(=O)C1=C(Cl)C(N)=NC(C2CC2)=N1 KWAIHLIXESXTJL-UHFFFAOYSA-N 0.000 claims description 8
- 239000003906 humectant Substances 0.000 claims description 8
- 230000001012 protector Effects 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 8
- 150000001204 N-oxides Chemical class 0.000 claims description 7
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 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 5
- 229910019142 PO4 Inorganic materials 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000010452 phosphate Substances 0.000 claims description 5
- 230000001681 protective effect Effects 0.000 claims description 5
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 claims description 4
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 claims description 3
- BTUSKWROSWXMPG-UHFFFAOYSA-N 6-amino-2-(4-bromophenyl)-5-chloropyrimidine-4-carboxylic acid Chemical compound OC(=O)C1=C(Cl)C(N)=NC(C=2C=CC(Br)=CC=2)=N1 BTUSKWROSWXMPG-UHFFFAOYSA-N 0.000 claims description 3
- DWIDAOMPDCVMCY-UHFFFAOYSA-N 6-amino-5-bromo-2-cyclopropylpyrimidine-4-carboxylic acid Chemical compound OC(=O)C1=C(Br)C(N)=NC(C2CC2)=N1 DWIDAOMPDCVMCY-UHFFFAOYSA-N 0.000 claims description 3
- IFNGRCNEIXJJOA-UHFFFAOYSA-N 6-amino-5-chloro-2-(4-chlorophenyl)pyrimidine-4-carboxylic acid Chemical compound OC(=O)C1=C(Cl)C(N)=NC(C=2C=CC(Cl)=CC=2)=N1 IFNGRCNEIXJJOA-UHFFFAOYSA-N 0.000 claims description 3
- NUFNQYOELLVIPL-UHFFFAOYSA-N acifluorfen Chemical compound C1=C([N+]([O-])=O)C(C(=O)O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 NUFNQYOELLVIPL-UHFFFAOYSA-N 0.000 claims description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 239000005532 Flumioxazine Substances 0.000 claims description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- ZFCHNZDUMIOWFV-UHFFFAOYSA-N pyrimidine-2-carboxylic acid Chemical compound OC(=O)C1=NC=CC=N1 ZFCHNZDUMIOWFV-UHFFFAOYSA-N 0.000 claims description 2
- 102100029028 Protoporphyrinogen oxidase Human genes 0.000 claims 2
- NSZKRXBJKXWLMN-UHFFFAOYSA-N 2-(4-chlorophenyl)pyrimidine-4-carboxylic acid Chemical compound OC(=O)C1=CC=NC(C=2C=CC(Cl)=CC=2)=N1 NSZKRXBJKXWLMN-UHFFFAOYSA-N 0.000 claims 1
- QUTYKIXIUDQOLK-PRJMDXOYSA-N 5-O-(1-carboxyvinyl)-3-phosphoshikimic acid Chemical compound O[C@H]1[C@H](OC(=C)C(O)=O)CC(C(O)=O)=C[C@H]1OP(O)(O)=O QUTYKIXIUDQOLK-PRJMDXOYSA-N 0.000 claims 1
- GFVYDJYJZMMZQS-UHFFFAOYSA-N methyl 5-chloro-2-cyclopropylpyrimidine-4-carboxylate Chemical compound C1=C(Cl)C(C(=O)OC)=NC(C2CC2)=N1 GFVYDJYJZMMZQS-UHFFFAOYSA-N 0.000 claims 1
- 239000005578 Mesotrione Substances 0.000 abstract description 3
- 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 abstract description 3
- 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 description 2
- PYKLUAIDKVVEOS-RAXLEYEMSA-N (e)-n-(cyanomethoxy)benzenecarboximidoyl cyanide Chemical compound N#CCO\N=C(\C#N)C1=CC=CC=C1 PYKLUAIDKVVEOS-RAXLEYEMSA-N 0.000 abstract 1
- AHXUVTKVCMOKIX-UHFFFAOYSA-N 1-bromo-4-(chloromethylsulfonyl)benzene Chemical compound ClCS(=O)(=O)C1=CC=C(Br)C=C1 AHXUVTKVCMOKIX-UHFFFAOYSA-N 0.000 abstract 1
- VYNOULHXXDFBLU-UHFFFAOYSA-N Cumyluron Chemical compound C=1C=CC=CC=1C(C)(C)NC(=O)NCC1=CC=CC=C1Cl VYNOULHXXDFBLU-UHFFFAOYSA-N 0.000 abstract 1
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- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 230000004222 uncontrolled growth Effects 0.000 description 1
- 241000701447 unidentified baculovirus Species 0.000 description 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 description 1
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- 235000013311 vegetables Nutrition 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 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
- A01N43/48—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
-
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
- A01N33/18—Nitro compounds
- A01N33/20—Nitro compounds containing oxygen or sulfur attached to the carbon skeleton containing the nitro group
- A01N33/22—Nitro compounds containing oxygen or sulfur attached to the carbon skeleton containing the nitro group having at least one oxygen or sulfur atom and at least one nitro group directly attached to the same aromatic ring system
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
-
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
- A01N39/04—Aryloxy-acetic acids; Derivatives 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 (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79065906P | 2006-04-10 | 2006-04-10 | |
| US85213906P | 2006-10-17 | 2006-10-17 | |
| PCT/US2007/008930 WO2007120706A2 (en) | 2006-04-10 | 2007-04-10 | Herbicidal mixtures |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2008012995A true MX2008012995A (es) | 2008-10-17 |
Family
ID=38450698
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2008012995A MX2008012995A (es) | 2006-04-10 | 2007-04-10 | Mezclas herbicidas. |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US20100285959A1 (enExample) |
| EP (1) | EP2003972A2 (enExample) |
| JP (1) | JP2009533448A (enExample) |
| KR (1) | KR20090024120A (enExample) |
| AR (1) | AR060415A1 (enExample) |
| AU (1) | AU2007238732A1 (enExample) |
| BR (1) | BRPI0709505A2 (enExample) |
| CA (1) | CA2646143A1 (enExample) |
| EA (1) | EA200870419A1 (enExample) |
| EC (1) | ECSP088802A (enExample) |
| IL (1) | IL193767A0 (enExample) |
| MA (1) | MA30396B1 (enExample) |
| MX (1) | MX2008012995A (enExample) |
| TN (1) | TNSN08519A1 (enExample) |
| WO (1) | WO2007120706A2 (enExample) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2514312B1 (en) * | 2007-08-27 | 2015-07-08 | Dow AgroSciences LLC | Synergistic herbicidal composition containing certain pyridine or pyrimidine carboxylic acids and certain cereal and rice herbicides |
| EP2327694B1 (en) | 2007-10-02 | 2013-07-24 | Dow AgroSciences LLC | Substituted 4-amino-picolinic acids and their use as herbicides |
| EP2052613A1 (de) * | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
| CN102118967B (zh) * | 2008-08-12 | 2014-04-02 | 杜邦公司 | 防治非期望的含羞草亚科植物的方法 |
| EP2191716A1 (de) | 2008-11-29 | 2010-06-02 | Bayer CropScience AG | Herbizid-Safener-Kombination |
| EP2191720A1 (de) | 2008-11-29 | 2010-06-02 | Bayer CropScience AG | Herbizid-Safener-Kombination |
| WO2010091353A2 (en) | 2009-02-06 | 2010-08-12 | University Of Tennessee Research Foundation | Novel herbicide resistance gene |
| AR079417A1 (es) * | 2009-10-29 | 2012-01-25 | Dow Agrosciences Llc | Proteccion del dano causado por el herbicida 6-amino-2-(fenil sustituido)-5-sustituido-4-pirimidincarboxilato en cultivo de cereales |
| AU2011254589B2 (en) | 2010-05-21 | 2015-04-30 | Bayer Intellectual Property Gmbh | Herbicidal agents for tolerant or resistant rape cultures |
| EP2571364A1 (de) | 2010-05-21 | 2013-03-27 | Bayer Intellectual Property GmbH | Herbizide mittel für tolerante oder resistente reiskulturen |
| WO2011144691A1 (de) | 2010-05-21 | 2011-11-24 | Bayer Cropscience Ag | Herbizide mittel für tolerante oder resistente maiskulturen |
| CN103025166A (zh) | 2010-05-21 | 2013-04-03 | 拜耳知识产权有限责任公司 | 用于耐受性或抗性谷物作物的除草剂 |
| GB2484982A (en) * | 2010-10-29 | 2012-05-02 | Syngenta Ltd | Safeners for a pyrimidine derivative herbicides |
| TWI596088B (zh) * | 2011-01-25 | 2017-08-21 | 陶氏農業科學公司 | ４－胺基－６－（經取代的苯基）吡啶甲酸酯及６－胺基－２－（經取代的苯基）－４－嘧啶羧酸酯之芳烷酯以及其等作為除草劑之用途 |
| US8962528B2 (en) | 2011-03-30 | 2015-02-24 | Dow Agrosciences, Llc. | Penoxsulam as an herbicide in alfalfa |
| RU2612301C2 (ru) | 2011-07-27 | 2017-03-06 | Байер Интеллектуэль Проперти Гмбх | Замещенные пиколиновые и пиримидин-4-карбоновые кислоты, способ их получения и их применение в качестве гербицидов и регуляторов роста растений |
| AR089283A1 (es) | 2011-12-27 | 2014-08-13 | Ishihara Sangyo Kaisha | Composicion herbicida |
| AU2013312913B2 (en) | 2012-09-04 | 2016-12-08 | Corteva Agriscience Llc | Synergistic weed control from applications of aminocyclopyrachlor and clopyralid |
| HK1212861A1 (zh) | 2012-09-28 | 2016-06-24 | 美国陶氏益农公司 | 來自施用環丙嘧啶酸和氯氨吡啶酸的協同雜草控制 |
| US9307762B2 (en) * | 2012-09-28 | 2016-04-12 | Dow Agrosciences Llc | Synergistic weed control from applications of aminocyclopyrachlor and fluroxypyr |
| BR102013024986B1 (pt) | 2012-09-28 | 2022-03-03 | Dow Agrosciences Llc | Método para controle de vegetação indesejável |
| WO2014071113A1 (en) * | 2012-11-05 | 2014-05-08 | Valent U.S.A. Corporation | Compositions and methods for residual weed control with ppo inhibitors and gibberellic acid |
| US9149037B2 (en) * | 2012-12-12 | 2015-10-06 | Dow Agrosciences Llc | Synergistic weed control from applications of aminocyclopyrachlor and 2,4 dichlorophenoxyacetic acid (2,4-D) |
| US9426991B2 (en) * | 2012-12-12 | 2016-08-30 | Dow Agrosciences Llc | Synergistic weed control from applications of aminocyclopyrachlor and picloram |
| US10412964B2 (en) | 2012-12-14 | 2019-09-17 | Dow Agrosciences Llc | Synergistic weed control from applications of aminopyralid and clopyralid |
| HUE042793T2 (hu) | 2012-12-14 | 2019-07-29 | Dow Agrosciences Llc | Szinergetikus gyomirtás aminopiralid és klopiralid alkalmazásával |
| BR102013032924B8 (pt) | 2012-12-21 | 2022-10-11 | Dow Agrosciences Llc | Composição herbicida, e método para controle de ervas daninhas |
| TR201818762T4 (tr) | 2012-12-21 | 2019-01-21 | Dow Agrosciences Llc | Sıcaklıkta stabil klokuintoset-meksil sulu bileşimler. |
| US9717244B2 (en) | 2013-02-25 | 2017-08-01 | Dow Agrosciences Llc | Methods of weed control in pineapple |
| WO2016044276A1 (en) | 2014-09-15 | 2016-03-24 | Dow Agrosciences Llc | Synergistic weed control from applications of pyridine carboxylic acid herbicides and photosystem ii inhibitors |
| TWI685302B (zh) | 2014-09-15 | 2020-02-21 | 美商陶氏農業科學公司 | 包含吡啶羧酸除草劑之安全的除草組成物 |
| AR101858A1 (es) * | 2014-09-15 | 2017-01-18 | Dow Agrosciences Llc | Composiciones herbicidas protegidas que comprenden un herbicida de ácido piridincarboxílico |
| TWI689252B (zh) * | 2014-09-15 | 2020-04-01 | 美商陶氏農業科學公司 | 源自於施用吡啶羧酸除草劑與乙醯乳酸合成酶（ａｌｓ）抑制劑的協同性雜草控制 |
| TWI689251B (zh) | 2014-09-15 | 2020-04-01 | 美商陶氏農業科學公司 | 源自於施用吡啶羧酸除草劑與合成生長素除草劑及/或生長素轉運抑制劑的協同性雜草控制 |
| WO2019046666A1 (en) * | 2017-09-01 | 2019-03-07 | Dow Agrosciences Llc | HERBICIDAL COMPOSITIONS CONTAINING PYRIDINE CARBOXYLIC ACIDS OR DERIVATIVES THEREOF, WITH GLYPHOSATE OR GLUFOSINATE OR DERIVATIVES THEREOF |
| BR102017019120B1 (pt) | 2017-09-06 | 2023-01-31 | UPL Corporation Limited | Mistura compreendendo um bioestimulante à base de folcisteína e um inseticida obtendo ação potencializadora dos resultados de ordens qualitativa, quantitativa e temporal observados em uma cultura agrícola de uma planta de interesse |
| WO2020172305A1 (en) | 2019-02-19 | 2020-08-27 | Gowan Company, L.L.C. | Stable liquid compositions and methods of using the same |
| CA3134115A1 (en) * | 2019-03-27 | 2020-10-01 | Sumitomo Chemical Company, Limited | Method for controlling weeds |
| JP7256332B2 (ja) | 2020-04-21 | 2023-04-11 | クミアイ化学工業株式会社 | メタン生成阻害剤組成物及びメタン生成の抑制方法 |
| MX2024009227A (es) * | 2022-01-31 | 2024-08-06 | Univ Arkansas | Tratamiento de semillas para proteger el trigo de los herbicidas de cloroacetamida. |
| PL248303B1 (pl) * | 2022-12-29 | 2025-11-24 | Uniwersytet Śląski W Katowicach | Kompozycja poprawiająca penetrację herbicydu przez powierzchnie części nadziemnych organów roślinnych |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH595061A5 (enExample) * | 1974-05-10 | 1978-01-31 | Ciba Geigy Ag | |
| EP0136976A3 (de) * | 1983-08-23 | 1985-05-15 | Ciba-Geigy Ag | Verwendung von Phenylpyrimidinen als Pflanzenregulatoren |
| AU2001265936B2 (en) * | 2000-05-22 | 2006-04-06 | Bayer Intellectual Property Gmbh | Selective heteroaryloxy-acetamide-based herbicides |
| TWI355894B (en) * | 2003-12-19 | 2012-01-11 | Du Pont | Herbicidal pyrimidines |
| EP1888536B1 (en) * | 2005-05-16 | 2010-04-28 | E.I. Du Pont De Nemours And Company | Process for preparing substituted pyrimidines |
-
2007
- 2007-04-10 AR ARP070101511A patent/AR060415A1/es not_active Application Discontinuation
- 2007-04-10 KR KR1020087027364A patent/KR20090024120A/ko not_active Ceased
- 2007-04-10 JP JP2009505457A patent/JP2009533448A/ja not_active Abandoned
- 2007-04-10 MX MX2008012995A patent/MX2008012995A/es not_active Application Discontinuation
- 2007-04-10 EP EP07755262A patent/EP2003972A2/en not_active Withdrawn
- 2007-04-10 AU AU2007238732A patent/AU2007238732A1/en not_active Abandoned
- 2007-04-10 US US12/296,474 patent/US20100285959A1/en not_active Abandoned
- 2007-04-10 EA EA200870419A patent/EA200870419A1/ru unknown
- 2007-04-10 WO PCT/US2007/008930 patent/WO2007120706A2/en not_active Ceased
- 2007-04-10 BR BRPI0709505-8A patent/BRPI0709505A2/pt not_active Application Discontinuation
- 2007-04-10 CA CA002646143A patent/CA2646143A1/en not_active Abandoned
-
2008
- 2008-08-28 IL IL193767A patent/IL193767A0/en unknown
- 2008-10-08 EC EC2008008802A patent/ECSP088802A/es unknown
- 2008-11-03 MA MA31350A patent/MA30396B1/fr unknown
- 2008-12-16 TN TNP2008000519A patent/TNSN08519A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2003972A2 (en) | 2008-12-24 |
| EA200870419A1 (ru) | 2009-02-27 |
| AU2007238732A1 (en) | 2007-10-25 |
| US20100285959A1 (en) | 2010-11-11 |
| IL193767A0 (en) | 2009-05-04 |
| ECSP088802A (es) | 2008-11-27 |
| AR060415A1 (es) | 2008-06-18 |
| CA2646143A1 (en) | 2007-10-25 |
| BRPI0709505A2 (pt) | 2011-07-19 |
| TNSN08519A1 (en) | 2010-04-14 |
| MA30396B1 (fr) | 2009-05-04 |
| JP2009533448A (ja) | 2009-09-17 |
| KR20090024120A (ko) | 2009-03-06 |
| WO2007120706A3 (en) | 2008-05-29 |
| WO2007120706A2 (en) | 2007-10-25 |
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Legal Events
| Date | Code | Title | Description |
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| FA | Abandonment or withdrawal |