AR112408A1 - Combinaciones herbicidas sinérgicas - Google Patents
Combinaciones herbicidas sinérgicasInfo
- Publication number
- AR112408A1 AR112408A1 ARP180102257A AR112408A1 AR 112408 A1 AR112408 A1 AR 112408A1 AR P180102257 A ARP180102257 A AR P180102257A AR 112408 A1 AR112408 A1 AR 112408A1
- Authority
- AR
- Argentina
- Prior art keywords
- herbicides
- herbicide
- group
- combinations
- combination
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract 12
- 230000002363 herbicidal effect Effects 0.000 title abstract 9
- 230000002195 synergetic effect Effects 0.000 title 1
- 229930192334 Auxin Natural products 0.000 abstract 4
- 239000002363 auxin Substances 0.000 abstract 4
- 239000003112 inhibitor Substances 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- UWHURBUBIHUHSU-UHFFFAOYSA-N 2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 UWHURBUBIHUHSU-UHFFFAOYSA-N 0.000 abstract 2
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 abstract 2
- 229940100389 Sulfonylurea Drugs 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 abstract 2
- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 abstract 2
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 abstract 2
- YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical compound BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 abstract 2
- -1 zuomihuanglong Chemical compound 0.000 abstract 2
- MZHCENGPTKEIGP-RXMQYKEDSA-N (R)-dichlorprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-RXMQYKEDSA-N 0.000 abstract 1
- 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 abstract 1
- 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 abstract 1
- IXWKBUKANTXHJH-UHFFFAOYSA-N 1-[5-chloro-2-methyl-4-(5-methyl-5,6-dihydro-1,4,2-dioxazin-3-yl)pyrazol-3-yl]sulfonyl-3-(4,6-dimethoxypyrimidin-2-yl)urea Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=C(Cl)C=2C=2OC(C)CON=2)C)=N1 IXWKBUKANTXHJH-UHFFFAOYSA-N 0.000 abstract 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 abstract 1
- 239000002794 2,4-DB Substances 0.000 abstract 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 abstract 1
- 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 abstract 1
- MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 abstract 1
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 abstract 1
- KFEFNHNXZQYTEW-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-4-methylbenzoic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=CC(C)=CC=C1C(O)=O KFEFNHNXZQYTEW-UHFFFAOYSA-N 0.000 abstract 1
- NUPJIGQFXCQJBK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-(methoxymethyl)nicotinic acid Chemical compound OC(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 NUPJIGQFXCQJBK-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- 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 abstract 1
- HCNBYBFTNHEQQJ-UHFFFAOYSA-N 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-6-(trifluoromethyl)pyridine-3-carboxylic acid Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(N=2)C(F)(F)F)C(O)=O)=N1 HCNBYBFTNHEQQJ-UHFFFAOYSA-N 0.000 abstract 1
- CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 abstract 1
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 abstract 1
- BCLGTIBYZQQFJW-UHFFFAOYSA-N 2-pyrimidin-2-ylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C1=NC=CC=N1 BCLGTIBYZQQFJW-UHFFFAOYSA-N 0.000 abstract 1
- MBFHUWCOCCICOK-UHFFFAOYSA-N 4-iodo-2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound 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 abstract 1
- PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 abstract 1
- 239000003666 Amidosulfuron Substances 0.000 abstract 1
- 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 abstract 1
- 239000005469 Azimsulfuron Substances 0.000 abstract 1
- 239000005488 Bispyribac Substances 0.000 abstract 1
- HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 abstract 1
- 239000005496 Chlorsulfuron Substances 0.000 abstract 1
- WMLPCIHUFDKWJU-UHFFFAOYSA-N Cinosulfuron Chemical compound COCCOC1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC)=NC(OC)=N1 WMLPCIHUFDKWJU-UHFFFAOYSA-N 0.000 abstract 1
- 239000005500 Clopyralid Substances 0.000 abstract 1
- OFSLKOLYLQSJPB-UHFFFAOYSA-N Cyclosulfamuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)NC=2C(=CC=CC=2)C(=O)C2CC2)=N1 OFSLKOLYLQSJPB-UHFFFAOYSA-N 0.000 abstract 1
- 239000005504 Dicamba Substances 0.000 abstract 1
- 239000005505 Dichlorprop-P Substances 0.000 abstract 1
- QNXAVFXEJCPCJO-UHFFFAOYSA-N Diclosulam Chemical compound N=1N2C(OCC)=NC(F)=CC2=NC=1S(=O)(=O)NC1=C(Cl)C=CC=C1Cl QNXAVFXEJCPCJO-UHFFFAOYSA-N 0.000 abstract 1
- UWVKRNOCDUPIDM-UHFFFAOYSA-N Ethoxysulfuron Chemical compound CCOC1=CC=CC=C1OS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 UWVKRNOCDUPIDM-UHFFFAOYSA-N 0.000 abstract 1
- 239000005514 Flazasulfuron Substances 0.000 abstract 1
- HWATZEJQIXKWQS-UHFFFAOYSA-N Flazasulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(F)(F)F)=N1 HWATZEJQIXKWQS-UHFFFAOYSA-N 0.000 abstract 1
- 239000005529 Florasulam Substances 0.000 abstract 1
- 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 abstract 1
- FICWGWVVIRLNRB-UHFFFAOYSA-N Flucetosulfuron Chemical compound COCC(=O)OC(C(C)F)C1=NC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 FICWGWVVIRLNRB-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- 239000005558 Fluroxypyr Substances 0.000 abstract 1
- 239000005560 Foramsulfuron Substances 0.000 abstract 1
- 239000005563 Halauxifen-methyl Substances 0.000 abstract 1
- 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 abstract 1
- 239000005566 Imazamox Substances 0.000 abstract 1
- 239000005981 Imazaquin Substances 0.000 abstract 1
- 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 abstract 1
- 239000005567 Imazosulfuron Substances 0.000 abstract 1
- NAGRVUXEKKZNHT-UHFFFAOYSA-N Imazosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N3C=CC=CC3=NC=2Cl)=N1 NAGRVUXEKKZNHT-UHFFFAOYSA-N 0.000 abstract 1
- 239000005568 Iodosulfuron Substances 0.000 abstract 1
- 239000005574 MCPA Substances 0.000 abstract 1
- 239000005575 MCPB Substances 0.000 abstract 1
- 101150039283 MCPB gene Proteins 0.000 abstract 1
- 239000005577 Mesosulfuron Substances 0.000 abstract 1
- 239000005582 Metosulam Substances 0.000 abstract 1
- VGHPMIFEKOFHHQ-UHFFFAOYSA-N Metosulam Chemical compound N1=C2N=C(OC)C=C(OC)N2N=C1S(=O)(=O)NC1=C(Cl)C=CC(C)=C1Cl VGHPMIFEKOFHHQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005592 Penoxsulam Substances 0.000 abstract 1
- SYJGKVOENHZYMQ-UHFFFAOYSA-N Penoxsulam Chemical compound N1=C2C(OC)=CN=C(OC)N2N=C1NS(=O)(=O)C1=C(OCC(F)F)C=CC=C1C(F)(F)F SYJGKVOENHZYMQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005595 Picloram Substances 0.000 abstract 1
- 239000005604 Prosulfuron Substances 0.000 abstract 1
- 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 abstract 1
- 239000005607 Pyroxsulam Substances 0.000 abstract 1
- 239000005608 Quinmerac Substances 0.000 abstract 1
- 239000005616 Rimsulfuron Substances 0.000 abstract 1
- 239000005619 Sulfosulfuron Substances 0.000 abstract 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 abstract 1
- 239000005626 Tribenuron Substances 0.000 abstract 1
- 239000005627 Triclopyr Substances 0.000 abstract 1
- 239000005628 Triflusulfuron Substances 0.000 abstract 1
- 239000005629 Tritosulfuron Substances 0.000 abstract 1
- MAHPNPYYQAIOJN-UHFFFAOYSA-N azimsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=CC=2C2=NN(C)N=N2)C)=N1 MAHPNPYYQAIOJN-UHFFFAOYSA-N 0.000 abstract 1
- PPWBRCCBKOWDNB-UHFFFAOYSA-N bensulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)CC=2C(=CC=CC=2)C(O)=O)=N1 PPWBRCCBKOWDNB-UHFFFAOYSA-N 0.000 abstract 1
- RYVIXQCRCQLFCM-UHFFFAOYSA-N bispyribac Chemical group COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C(O)=O)=N1 RYVIXQCRCQLFCM-UHFFFAOYSA-N 0.000 abstract 1
- RIUXZHMCCFLRBI-UHFFFAOYSA-N chlorimuron Chemical compound COC1=CC(Cl)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 RIUXZHMCCFLRBI-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 abstract 1
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 abstract 1
- IRLGCAJYYKDTCG-UHFFFAOYSA-N ethametsulfuron Chemical compound CCOC1=NC(NC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 IRLGCAJYYKDTCG-UHFFFAOYSA-N 0.000 abstract 1
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- KDHKOPYYWOHESS-UHFFFAOYSA-N halauxifen-methyl Chemical group NC1=C(Cl)C(C(=O)OC)=NC(C=2C(=C(OC)C(Cl)=CC=2)F)=C1 KDHKOPYYWOHESS-UHFFFAOYSA-N 0.000 abstract 1
- AIMMSOZBPYFASU-UHFFFAOYSA-N n-(4,6-dimethoxypyrimidin-2-yl)-n'-[3-(2,2,2-trifluoroethoxy)pyridin-1-ium-2-yl]sulfonylcarbamimidate Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)OCC(F)(F)F)=N1 AIMMSOZBPYFASU-UHFFFAOYSA-N 0.000 abstract 1
- GLBLPMUBLHYFCW-UHFFFAOYSA-N n-(5,7-dimethoxy-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-2-methoxy-4-(trifluoromethyl)pyridine-3-sulfonamide Chemical compound N1=C2N=C(OC)C=C(OC)N2N=C1NS(=O)(=O)C1=C(OC)N=CC=C1C(F)(F)F GLBLPMUBLHYFCW-UHFFFAOYSA-N 0.000 abstract 1
- ONDBSQWZWRGVIL-UHFFFAOYSA-N o-pyrimidin-2-yl benzenecarbothioate Chemical compound C=1C=CC=CC=1C(=S)OC1=NC=CC=N1 ONDBSQWZWRGVIL-UHFFFAOYSA-N 0.000 abstract 1
- DEIKMOQTJBGGAX-DJKKODMXSA-N pyriminobac Chemical compound CO\N=C(/C)C1=CC=CC(OC=2N=C(OC)C=C(OC)N=2)=C1C(O)=O DEIKMOQTJBGGAX-DJKKODMXSA-N 0.000 abstract 1
- FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 abstract 1
- ALZOLUNSQWINIR-UHFFFAOYSA-N quinmerac Chemical compound OC(=O)C1=C(Cl)C=CC2=CC(C)=CN=C21 ALZOLUNSQWINIR-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- FZMKKCQHDROFNI-UHFFFAOYSA-N sulfometuron Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 FZMKKCQHDROFNI-UHFFFAOYSA-N 0.000 abstract 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 abstract 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 abstract 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 abstract 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 abstract 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 abstract 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
- 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
- A01N37/36—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom 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
- 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
-
- 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
-
- 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
-
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
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)
Abstract
Una combinación herbicida que comprende al menos dos auxinas sintéticas o al menos dos auxinas sintéticas con al menos un inhibidor de ALS, una composición que comprende estas combinaciones, un método de uso de estas combinaciones y un kit que comprende los componentes de estas combinaciones. Reivindicación 1: Una combinación herbicida caracterizada porque comprende al menos dos herbicidas de auxina sintética y al menos un herbicida inhibidor de ALS. Reivindicación 2: La combinación como se reivindica en la reivindicación 1, caracterizada porque al menos dos herbicidas de auxina se seleccionan del grupo que consiste en (2,4-D); 2,4-DB; dicamba; clorambén; 2,4,5-T; clomeprop; diclorprop; diclorprop-P; MCPA; MCPB; mecoprop; aminopiralida; clopiralida; fluroxipir; halauxifen-metil; picloram; triclopir; aminociclopiraclor; quinclorac; quinmerac y sus sales; y ésteres de estos. Reivindicación 4: La combinación como se reivindica en las reivindicaciones 1 - 3, caracterizada porque el inhibidor de ALS se selecciona de herbicidas de sulfonilurea, o herbicidas de imidazolinona, herbicidas de triazolopirimidina, y herbicidas de pirimidinil tiobenzoato, en donde: el herbicida de sulfonilurea se selecciona del grupo que consiste en amidosulfurón, azimsulfurón, bensulfurón, clorimurón, ciclosulfamurón, etoxisulfurón, flazasulfurón, flucetosulfurón, flupirsulfurón, foramsulfurón, halosulfurón, imazosulfurón, mesosulfurón, metazosulfurón, metiopirisulfurón, monosulfurón, nicosulfurón, ortosulfamurón, oxasulfurón, primisulfurón, propirisulfurón, pirazosulfurón, rimsulfurón, sulfometurón, sulfosulfurón, trifloxisulfurón, zuomihuanglong, clorsulfurón, cinosulfurón, etametsulfurón, yodosulfurón, iofensulfurón, metsulfurón, prosulfurón, tifensulfurón, triasulfurón, tribenurón, triflusulfurón, y tritosulfurón; el herbicida de imidazolinona se selecciona del grupo que consiste en imazametabenz, imazamox, imazapic, imazapir, imazaquin e imazetapir; el herbicida de triazolopirimidina se selecciona del grupo que consiste en cloransulam, diclosulam, florasulam, flumetsulam, metosulam, penoxsulam y piroxsulam; y el herbicida de ácido pirimidinil benzoico se selecciona de bispiribac, piriminobac y piritiobac. Reivindicación 5: Una combinación herbicida caracterizada porque comprende ácido 2,4-D o una sal de este, ácido picloram o una sal de este y metsulfurón o un éster de este.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN201731028212 | 2017-08-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR112408A1 true AR112408A1 (es) | 2019-10-23 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP180102257 AR112408A1 (es) | 2017-08-08 | 2018-08-08 | Combinaciones herbicidas sinérgicas |
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| Country | Link |
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| US (1) | US20210392896A1 (es) |
| EP (1) | EP3664609A4 (es) |
| AR (1) | AR112408A1 (es) |
| AU (1) | AU2018315717B2 (es) |
| BR (1) | BR102018016173A2 (es) |
| CA (1) | CA3071954A1 (es) |
| CL (1) | CL2020000318A1 (es) |
| CO (1) | CO2020001325A2 (es) |
| EA (1) | EA202090335A1 (es) |
| EC (1) | ECSP20009753A (es) |
| IL (1) | IL272148A (es) |
| MX (1) | MX2020001557A (es) |
| PE (1) | PE20200667A1 (es) |
| UA (1) | UA125860C2 (es) |
| UY (1) | UY37836A (es) |
| WO (1) | WO2019030614A1 (es) |
| ZA (1) | ZA202000684B (es) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2020009719A (es) * | 2018-03-29 | 2020-10-07 | Upl Ltd | Composiciones agroquimicas solidas. |
| CN114615890B (zh) * | 2019-09-13 | 2024-02-13 | 安道麦阿甘有限公司 | 包含氨基吡啶和喹草酸的除草混合物 |
| CN113661997A (zh) * | 2021-08-26 | 2021-11-19 | 安徽省圣丹生物化工有限公司 | 一种基于二氯喹啉酸的复合除草剂 |
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| US5221319A (en) * | 1991-08-16 | 1993-06-22 | Pbi-Gordon Corporation | Dry, water-soluble, substituted phenoxy and/or benzoic acid herbicidal compositions and method of preparing same |
| LT2740360T (lt) * | 2008-06-18 | 2018-03-12 | Basf Se | Trijų komponentų herbicidinės kompozicijos, apimančios aminopiralidiną ir imazamoksą |
| US9426991B2 (en) * | 2012-12-12 | 2016-08-30 | Dow Agrosciences Llc | Synergistic weed control from applications of aminocyclopyrachlor and picloram |
| US20140235444A1 (en) * | 2013-02-19 | 2014-08-21 | Dow Agrosciences Llc | Synergistic supression of grass seedhead production from applications of aminocyclopyrachlor and metsulfuron |
| WO2014138177A1 (en) * | 2013-03-06 | 2014-09-12 | Dow Agrosciences Llc | Method for controlling weeds in turf |
| AU2014327408B2 (en) * | 2013-09-26 | 2018-02-15 | Basf Agrochemical Products B.V. | Method for controlling weeds in sugar cane plantations |
| CN104542663A (zh) * | 2014-12-23 | 2015-04-29 | 江西中迅农化有限公司 | 氯吡嘧磺隆和二氯喹啉酸及氯氟吡氧乙酸的除草组合物 |
| CN106472529A (zh) * | 2016-08-31 | 2017-03-08 | 四川利尔作物科学有限公司 | 除草组合物及其应用 |
| MX2020009719A (es) * | 2018-03-29 | 2020-10-07 | Upl Ltd | Composiciones agroquimicas solidas. |
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2018
- 2018-07-31 UA UAA202001055A patent/UA125860C2/uk unknown
- 2018-07-31 WO PCT/IB2018/055716 patent/WO2019030614A1/en unknown
- 2018-07-31 CA CA3071954A patent/CA3071954A1/en active Pending
- 2018-07-31 US US16/637,352 patent/US20210392896A1/en active Pending
- 2018-07-31 MX MX2020001557A patent/MX2020001557A/es unknown
- 2018-07-31 PE PE2020000197A patent/PE20200667A1/es unknown
- 2018-07-31 EA EA202090335A patent/EA202090335A1/ru unknown
- 2018-07-31 AU AU2018315717A patent/AU2018315717B2/en active Active
- 2018-07-31 EP EP18844319.6A patent/EP3664609A4/en active Pending
- 2018-08-07 UY UY0001037836A patent/UY37836A/es unknown
- 2018-08-08 AR ARP180102257 patent/AR112408A1/es active IP Right Grant
- 2018-08-08 BR BR102018016173-3A patent/BR102018016173A2/pt not_active Application Discontinuation
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2020
- 2020-01-20 IL IL272148A patent/IL272148A/en unknown
- 2020-01-31 ZA ZA2020/00684A patent/ZA202000684B/en unknown
- 2020-02-06 CO CONC2020/0001325A patent/CO2020001325A2/es unknown
- 2020-02-06 CL CL2020000318A patent/CL2020000318A1/es unknown
- 2020-02-07 EC ECSENADI20209753A patent/ECSP20009753A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR102018016173A2 (pt) | 2019-03-26 |
| PE20200667A1 (es) | 2020-06-11 |
| CL2020000318A1 (es) | 2020-08-14 |
| AU2018315717A1 (en) | 2020-02-06 |
| CA3071954A1 (en) | 2019-02-14 |
| ZA202000684B (en) | 2021-01-27 |
| MX2020001557A (es) | 2020-03-20 |
| IL272148A (en) | 2020-03-31 |
| CO2020001325A2 (es) | 2020-04-01 |
| AU2018315717B2 (en) | 2023-07-13 |
| EP3664609A4 (en) | 2021-04-28 |
| UA125860C2 (uk) | 2022-06-22 |
| ECSP20009753A (es) | 2020-04-22 |
| UY37836A (es) | 2019-01-31 |
| WO2019030614A1 (en) | 2019-02-14 |
| US20210392896A1 (en) | 2021-12-23 |
| EA202090335A1 (ru) | 2020-05-18 |
| EP3664609A1 (en) | 2020-06-17 |
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