AR035747A1 - HERBICIDE PREPARATION LIQUID CONCENTRATED IN THE FORM OF EMULSION AND PROCESS TO CONTROL GROWTH OR TO ELIMINATE INDESEABLE VEGETATION - Google Patents
HERBICIDE PREPARATION LIQUID CONCENTRATED IN THE FORM OF EMULSION AND PROCESS TO CONTROL GROWTH OR TO ELIMINATE INDESEABLE VEGETATIONInfo
- Publication number
- AR035747A1 AR035747A1 ARP020100503A ARP020100503A AR035747A1 AR 035747 A1 AR035747 A1 AR 035747A1 AR P020100503 A ARP020100503 A AR P020100503A AR P020100503 A ARP020100503 A AR P020100503A AR 035747 A1 AR035747 A1 AR 035747A1
- Authority
- AR
- Argentina
- Prior art keywords
- triathlonol
- methylpropylchine
- chlo
- methyl
- ethyl
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title abstract 7
- 239000004009 herbicide Substances 0.000 title abstract 7
- 239000000839 emulsion Substances 0.000 title abstract 3
- 239000007788 liquid Substances 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- -1 benzfendizona Chemical compound 0.000 abstract 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 abstract 3
- 235000019270 ammonium chloride Nutrition 0.000 abstract 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 abstract 2
- MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 abstract 2
- 239000004094 surface-active agent Substances 0.000 abstract 2
- 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
- BXKKQFGRMSOANI-UHFFFAOYSA-N 1-methoxy-3-[4-[(2-methoxy-2,4,4-trimethyl-3h-chromen-7-yl)oxy]phenyl]-1-methylurea Chemical compound C1=CC(NC(=O)N(C)OC)=CC=C1OC1=CC=C2C(C)(C)CC(C)(OC)OC2=C1 BXKKQFGRMSOANI-UHFFFAOYSA-N 0.000 abstract 1
- KGKGSIUWJCAFPX-UHFFFAOYSA-N 2,6-dichlorothiobenzamide Chemical compound NC(=S)C1=C(Cl)C=CC=C1Cl KGKGSIUWJCAFPX-UHFFFAOYSA-N 0.000 abstract 1
- 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 1
- 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 abstract 1
- IRCMYGHHKLLGHV-UHFFFAOYSA-N 2-ethoxy-3,3-dimethyl-2,3-dihydro-1-benzofuran-5-yl methanesulfonate Chemical compound C1=C(OS(C)(=O)=O)C=C2C(C)(C)C(OCC)OC2=C1 IRCMYGHHKLLGHV-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- NYRMIJKDBAQCHC-UHFFFAOYSA-N 5-(methylamino)-2-phenyl-4-[3-(trifluoromethyl)phenyl]furan-3(2H)-one Chemical compound O1C(NC)=C(C=2C=C(C=CC=2)C(F)(F)F)C(=O)C1C1=CC=CC=C1 NYRMIJKDBAQCHC-UHFFFAOYSA-N 0.000 abstract 1
- DVOODWOZJVJKQR-UHFFFAOYSA-N 5-tert-butyl-3-(2,4-dichloro-5-prop-2-ynoxyphenyl)-1,3,4-oxadiazol-2-one Chemical group O=C1OC(C(C)(C)C)=NN1C1=CC(OCC#C)=C(Cl)C=C1Cl DVOODWOZJVJKQR-UHFFFAOYSA-N 0.000 abstract 1
- VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 abstract 1
- XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-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
- NXQDBZGWYSEGFL-UHFFFAOYSA-N Anilofos Chemical compound COP(=S)(OC)SCC(=O)N(C(C)C)C1=CC=C(Cl)C=C1 NXQDBZGWYSEGFL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005469 Azimsulfuron Substances 0.000 abstract 1
- 239000005471 Benfluralin Substances 0.000 abstract 1
- QGQSRQPXXMTJCM-UHFFFAOYSA-N Benfuresate Chemical compound CCS(=O)(=O)OC1=CC=C2OCC(C)(C)C2=C1 QGQSRQPXXMTJCM-UHFFFAOYSA-N 0.000 abstract 1
- RRNIZKPFKNDSRS-UHFFFAOYSA-N Bensulide Chemical compound CC(C)OP(=S)(OC(C)C)SCCNS(=O)(=O)C1=CC=CC=C1 RRNIZKPFKNDSRS-UHFFFAOYSA-N 0.000 abstract 1
- JDWQITFHZOBBFE-UHFFFAOYSA-N Benzofenap Chemical compound C=1C=C(Cl)C(C)=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=C(C)C=C1 JDWQITFHZOBBFE-UHFFFAOYSA-N 0.000 abstract 1
- OEYOMNZEMCPTKN-UHFFFAOYSA-N Butamifos Chemical compound CCC(C)NP(=S)(OCC)OC1=CC(C)=CC=C1[N+]([O-])=O OEYOMNZEMCPTKN-UHFFFAOYSA-N 0.000 abstract 1
- SPNQRCTZKIBOAX-UHFFFAOYSA-N Butralin Chemical compound CCC(C)NC1=C([N+]([O-])=O)C=C(C(C)(C)C)C=C1[N+]([O-])=O SPNQRCTZKIBOAX-UHFFFAOYSA-N 0.000 abstract 1
- BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 abstract 1
- 239000005490 Carbetamide Substances 0.000 abstract 1
- NLYNUTMZTCLNOO-UHFFFAOYSA-N Chlorbromuron Chemical compound CON(C)C(=O)NC1=CC=C(Br)C(Cl)=C1 NLYNUTMZTCLNOO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005494 Chlorotoluron Substances 0.000 abstract 1
- DFCAFRGABIXSDS-UHFFFAOYSA-N Cycloate Chemical compound CCSC(=O)N(CC)C1CCCCC1 DFCAFRGABIXSDS-UHFFFAOYSA-N 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
- NNYRZQHKCHEXSD-UHFFFAOYSA-N Daimuron Chemical compound C1=CC(C)=CC=C1NC(=O)NC(C)(C)C1=CC=CC=C1 NNYRZQHKCHEXSD-UHFFFAOYSA-N 0.000 abstract 1
- 239000005507 Diflufenican Substances 0.000 abstract 1
- DHWRNDJOGMTCPB-UHFFFAOYSA-N Dimefuron Chemical compound ClC1=CC(NC(=O)N(C)C)=CC=C1N1C(=O)OC(C(C)(C)C)=N1 DHWRNDJOGMTCPB-UHFFFAOYSA-N 0.000 abstract 1
- OFDYMSKSGFSLLM-UHFFFAOYSA-N Dinitramine Chemical compound CCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C(N)=C1[N+]([O-])=O OFDYMSKSGFSLLM-UHFFFAOYSA-N 0.000 abstract 1
- IIPZYDQGBIWLBU-UHFFFAOYSA-N Dinoterb Chemical compound CC(C)(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O IIPZYDQGBIWLBU-UHFFFAOYSA-N 0.000 abstract 1
- QAHFOPIILNICLA-UHFFFAOYSA-N Diphenamid Chemical compound C=1C=CC=CC=1C(C(=O)N(C)C)C1=CC=CC=C1 QAHFOPIILNICLA-UHFFFAOYSA-N 0.000 abstract 1
- 239000005510 Diuron Substances 0.000 abstract 1
- GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 abstract 1
- BXEHUCNTIZGSOJ-UHFFFAOYSA-N Esprocarb Chemical compound CC(C)C(C)N(CC)C(=O)SCC1=CC=CC=C1 BXEHUCNTIZGSOJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005512 Ethofumesate Substances 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
- 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
- 239000005533 Fluometuron Substances 0.000 abstract 1
- AOQMRUTZEYVDIL-UHFFFAOYSA-N Flupoxam Chemical compound C=1C=C(Cl)C(COCC(F)(F)C(F)(F)F)=CC=1N1N=C(C(=O)N)N=C1C1=CC=CC=C1 AOQMRUTZEYVDIL-UHFFFAOYSA-N 0.000 abstract 1
- GXAMYUGOODKVRM-UHFFFAOYSA-N Flurecol Chemical compound C1=CC=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 GXAMYUGOODKVRM-UHFFFAOYSA-N 0.000 abstract 1
- YWBVHLJPRPCRSD-UHFFFAOYSA-N Fluridone Chemical compound O=C1C(C=2C=C(C=CC=2)C(F)(F)F)=CN(C)C=C1C1=CC=CC=C1 YWBVHLJPRPCRSD-UHFFFAOYSA-N 0.000 abstract 1
- 239000005558 Fluroxypyr Substances 0.000 abstract 1
- 239000005559 Flurtamone 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
- CAWXEEYDBZRFPE-UHFFFAOYSA-N Hexazinone Chemical compound O=C1N(C)C(N(C)C)=NC(=O)N1C1CCCCC1 CAWXEEYDBZRFPE-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
- PMAAYIYCDXGUAP-UHFFFAOYSA-N Indanofan Chemical compound O=C1C2=CC=CC=C2C(=O)C1(CC)CC1(C=2C=C(Cl)C=CC=2)CO1 PMAAYIYCDXGUAP-UHFFFAOYSA-N 0.000 abstract 1
- JLLJHQLUZAKJFH-UHFFFAOYSA-N Isouron Chemical compound CN(C)C(=O)NC=1C=C(C(C)(C)C)ON=1 JLLJHQLUZAKJFH-UHFFFAOYSA-N 0.000 abstract 1
- 239000005570 Isoxaben Substances 0.000 abstract 1
- 239000005571 Isoxaflutole Substances 0.000 abstract 1
- 239000005572 Lenacil Substances 0.000 abstract 1
- 239000005573 Linuron Substances 0.000 abstract 1
- 239000005579 Metamitron Substances 0.000 abstract 1
- 239000005580 Metazachlor Substances 0.000 abstract 1
- RRVIAQKBTUQODI-UHFFFAOYSA-N Methabenzthiazuron Chemical compound C1=CC=C2SC(N(C)C(=O)NC)=NC2=C1 RRVIAQKBTUQODI-UHFFFAOYSA-N 0.000 abstract 1
- FMINYZXVCTYSNY-UHFFFAOYSA-N Methyldymron Chemical compound C=1C=CC=CC=1N(C)C(=O)NC(C)(C)C1=CC=CC=C1 FMINYZXVCTYSNY-UHFFFAOYSA-N 0.000 abstract 1
- 239000005581 Metobromuron Substances 0.000 abstract 1
- WLFDQEVORAMCIM-UHFFFAOYSA-N Metobromuron Chemical compound CON(C)C(=O)NC1=CC=C(Br)C=C1 WLFDQEVORAMCIM-UHFFFAOYSA-N 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
- 239000005583 Metribuzin Substances 0.000 abstract 1
- LKJPSUCKSLORMF-UHFFFAOYSA-N Monolinuron Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C=C1 LKJPSUCKSLORMF-UHFFFAOYSA-N 0.000 abstract 1
- WXZVAROIGSFCFJ-UHFFFAOYSA-N N,N-diethyl-2-(naphthalen-1-yloxy)propanamide Chemical compound C1=CC=C2C(OC(C)C(=O)N(CC)CC)=CC=CC2=C1 WXZVAROIGSFCFJ-UHFFFAOYSA-N 0.000 abstract 1
- LVKTWOXHRYGDMM-UHFFFAOYSA-N Naproanilide Chemical compound C=1C=C2C=CC=CC2=CC=1OC(C)C(=O)NC1=CC=CC=C1 LVKTWOXHRYGDMM-UHFFFAOYSA-N 0.000 abstract 1
- 239000005585 Napropamide Substances 0.000 abstract 1
- CCGPUGMWYLICGL-UHFFFAOYSA-N Neburon Chemical compound CCCCN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 CCGPUGMWYLICGL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005586 Nicosulfuron Substances 0.000 abstract 1
- 239000005587 Oryzalin Substances 0.000 abstract 1
- 239000005588 Oxadiazon Substances 0.000 abstract 1
- CHNUNORXWHYHNE-UHFFFAOYSA-N Oxadiazon Chemical compound C1=C(Cl)C(OC(C)C)=CC(N2C(OC(=N2)C(C)(C)C)=O)=C1Cl CHNUNORXWHYHNE-UHFFFAOYSA-N 0.000 abstract 1
- 239000005589 Oxasulfuron Substances 0.000 abstract 1
- 239000005591 Pendimethalin Substances 0.000 abstract 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 abstract 1
- UNLYSVIDNRIVFJ-UHFFFAOYSA-N Piperophos Chemical compound CCCOP(=S)(OCCC)SCC(=O)N1CCCCC1C UNLYSVIDNRIVFJ-UHFFFAOYSA-N 0.000 abstract 1
- YLPGTOIOYRQOHV-UHFFFAOYSA-N Pretilachlor Chemical compound CCCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC YLPGTOIOYRQOHV-UHFFFAOYSA-N 0.000 abstract 1
- GPGLBXMQFQQXDV-UHFFFAOYSA-N Primisulfuron Chemical compound OC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC(F)F)=CC(OC(F)F)=N1 GPGLBXMQFQQXDV-UHFFFAOYSA-N 0.000 abstract 1
- RSVPPPHXAASNOL-UHFFFAOYSA-N Prodiamine Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C(N)=C1[N+]([O-])=O RSVPPPHXAASNOL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005606 Pyridate Substances 0.000 abstract 1
- JTZCTMAVMHRNTR-UHFFFAOYSA-N Pyridate Chemical compound CCCCCCCCSC(=O)OC1=CC(Cl)=NN=C1C1=CC=CC=C1 JTZCTMAVMHRNTR-UHFFFAOYSA-N 0.000 abstract 1
- 239000005608 Quinmerac Substances 0.000 abstract 1
- 239000005616 Rimsulfuron Substances 0.000 abstract 1
- JXVIIQLNUPXOII-UHFFFAOYSA-N Siduron Chemical compound CC1CCCCC1NC(=O)NC1=CC=CC=C1 JXVIIQLNUPXOII-UHFFFAOYSA-N 0.000 abstract 1
- 239000005618 Sulcotrione Substances 0.000 abstract 1
- 239000005619 Sulfosulfuron Substances 0.000 abstract 1
- HBPDKDSFLXWOAE-UHFFFAOYSA-N Tebuthiuron Chemical compound CNC(=O)N(C)C1=NN=C(C(C)(C)C)S1 HBPDKDSFLXWOAE-UHFFFAOYSA-N 0.000 abstract 1
- YIJZJEYQBAAWRJ-UHFFFAOYSA-N Thiazopyr Chemical compound N1=C(C(F)F)C(C(=O)OC)=C(CC(C)C)C(C=2SCCN=2)=C1C(F)(F)F YIJZJEYQBAAWRJ-UHFFFAOYSA-N 0.000 abstract 1
- QHTQREMOGMZHJV-UHFFFAOYSA-N Thiobencarb Chemical compound CCN(CC)C(=O)SCC1=CC=C(Cl)C=C1 QHTQREMOGMZHJV-UHFFFAOYSA-N 0.000 abstract 1
- AMRQXHFXNZFDCH-SECBINFHSA-N [(2r)-1-(ethylamino)-1-oxopropan-2-yl] n-phenylcarbamate Chemical compound CCNC(=O)[C@@H](C)OC(=O)NC1=CC=CC=C1 AMRQXHFXNZFDCH-SECBINFHSA-N 0.000 abstract 1
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 abstract 1
- 229910001514 alkali metal chloride Inorganic materials 0.000 abstract 1
- RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 abstract 1
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 abstract 1
- XOEMATDHVZOBSG-UHFFFAOYSA-N azafenidin Chemical compound C1=C(OCC#C)C(Cl)=CC(Cl)=C1N1C(=O)N2CCCCC2=N1 XOEMATDHVZOBSG-UHFFFAOYSA-N 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
- SMDHCQAYESWHAE-UHFFFAOYSA-N benfluralin Chemical compound CCCCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O SMDHCQAYESWHAE-UHFFFAOYSA-N 0.000 abstract 1
- XMQFTWRPUQYINF-UHFFFAOYSA-N bensulfuron-methyl Chemical compound COC(=O)C1=CC=CC=C1CS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 XMQFTWRPUQYINF-UHFFFAOYSA-N 0.000 abstract 1
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- JEDYYFXHPAIBGR-UHFFFAOYSA-N butafenacil Chemical compound O=C1N(C)C(C(F)(F)F)=CC(=O)N1C1=CC=C(Cl)C(C(=O)OC(C)(C)C(=O)OCC=C)=C1 JEDYYFXHPAIBGR-UHFFFAOYSA-N 0.000 abstract 1
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- 230000015556 catabolic process Effects 0.000 abstract 1
- WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 abstract 1
- 150000001805 chlorine compounds Chemical class 0.000 abstract 1
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- 238000006731 degradation reaction Methods 0.000 abstract 1
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- 238000007865 diluting Methods 0.000 abstract 1
- BWUPSGJXXPATLU-UHFFFAOYSA-N dimepiperate Chemical compound C=1C=CC=CC=1C(C)(C)SC(=O)N1CCCCC1 BWUPSGJXXPATLU-UHFFFAOYSA-N 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 abstract 1
- XXOYNJXVWVNOOJ-UHFFFAOYSA-N fenuron Chemical compound CN(C)C(=O)NC1=CC=CC=C1 XXOYNJXVWVNOOJ-UHFFFAOYSA-N 0.000 abstract 1
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- RZILCCPWPBTYDO-UHFFFAOYSA-N fluometuron Chemical compound CN(C)C(=O)NC1=CC=CC(C(F)(F)F)=C1 RZILCCPWPBTYDO-UHFFFAOYSA-N 0.000 abstract 1
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- PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 abstract 1
- PMHURSZHKKJGBM-UHFFFAOYSA-N isoxaben Chemical compound O1N=C(C(C)(CC)CC)C=C1NC(=O)C1=C(OC)C=CC=C1OC PMHURSZHKKJGBM-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- 229940088649 isoxaflutole Drugs 0.000 abstract 1
- ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 abstract 1
- XIGAUIHYSDTJHW-UHFFFAOYSA-N mefenacet Chemical compound N=1C2=CC=CC=C2SC=1OCC(=O)N(C)C1=CC=CC=C1 XIGAUIHYSDTJHW-UHFFFAOYSA-N 0.000 abstract 1
- VHCNQEUWZYOAEV-UHFFFAOYSA-N metamitron Chemical compound O=C1N(N)C(C)=NN=C1C1=CC=CC=C1 VHCNQEUWZYOAEV-UHFFFAOYSA-N 0.000 abstract 1
- STEPQTYSZVCJPV-UHFFFAOYSA-N metazachlor Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CN1N=CC=C1 STEPQTYSZVCJPV-UHFFFAOYSA-N 0.000 abstract 1
- DSRNRYQBBJQVCW-UHFFFAOYSA-N metoxuron Chemical compound COC1=CC=C(NC(=O)N(C)C)C=C1Cl DSRNRYQBBJQVCW-UHFFFAOYSA-N 0.000 abstract 1
- FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 abstract 1
- DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 abstract 1
- CHEDHKBPPDKBQF-UPONEAKYSA-N n-[5-[(6s,7ar)-6-fluoro-1,3-dioxo-5,6,7,7a-tetrahydropyrrolo[1,2-c]imidazol-2-yl]-2-chloro-4-fluorophenyl]-1-chloromethanesulfonamide Chemical compound N1([C@@H](C2=O)C[C@@H](C1)F)C(=O)N2C1=CC(NS(=O)(=O)CCl)=C(Cl)C=C1F CHEDHKBPPDKBQF-UPONEAKYSA-N 0.000 abstract 1
- 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 abstract 1
- NVGOPFQZYCNLDU-UHFFFAOYSA-N norflurazon Chemical compound O=C1C(Cl)=C(NC)C=NN1C1=CC=CC(C(F)(F)F)=C1 NVGOPFQZYCNLDU-UHFFFAOYSA-N 0.000 abstract 1
- LLLFASISUZUJEQ-UHFFFAOYSA-N orbencarb Chemical compound CCN(CC)C(=O)SCC1=CC=CC=C1Cl LLLFASISUZUJEQ-UHFFFAOYSA-N 0.000 abstract 1
- UNAHYJYOSSSJHH-UHFFFAOYSA-N oryzalin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(N)(=O)=O)C=C1[N+]([O-])=O UNAHYJYOSSSJHH-UHFFFAOYSA-N 0.000 abstract 1
- IOXAXYHXMLCCJJ-UHFFFAOYSA-N oxetan-3-yl 2-[(4,6-dimethylpyrimidin-2-yl)carbamoylsulfamoyl]benzoate Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(=O)OC2COC2)=N1 IOXAXYHXMLCCJJ-UHFFFAOYSA-N 0.000 abstract 1
- CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 abstract 1
- ISEUFVQQFVOBCY-UHFFFAOYSA-N prometon Chemical compound COC1=NC(NC(C)C)=NC(NC(C)C)=N1 ISEUFVQQFVOBCY-UHFFFAOYSA-N 0.000 abstract 1
- MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 abstract 1
- FKLQIONHGSFYJY-UHFFFAOYSA-N propan-2-yl 5-[4-bromo-1-methyl-5-(trifluoromethyl)pyrazol-3-yl]-2-chloro-4-fluorobenzoate Chemical compound C1=C(Cl)C(C(=O)OC(C)C)=CC(C=2C(=C(N(C)N=2)C(F)(F)F)Br)=C1F FKLQIONHGSFYJY-UHFFFAOYSA-N 0.000 abstract 1
- WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 abstract 1
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 abstract 1
- FKERUJTUOYLBKB-UHFFFAOYSA-N pyrazoxyfen Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=CC=C1 FKERUJTUOYLBKB-UHFFFAOYSA-N 0.000 abstract 1
- 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 1
- 125000001453 quaternary ammonium group Chemical group 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
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 abstract 1
- 230000000087 stabilizing effect Effects 0.000 abstract 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 abstract 1
- 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 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
- RJKCKKDSSSRYCB-UHFFFAOYSA-N tebutam Chemical compound CC(C)(C)C(=O)N(C(C)C)CC1=CC=CC=C1 RJKCKKDSSSRYCB-UHFFFAOYSA-N 0.000 abstract 1
- BCQMBFHBDZVHKU-UHFFFAOYSA-N terbumeton Chemical compound CCNC1=NC(NC(C)(C)C)=NC(OC)=N1 BCQMBFHBDZVHKU-UHFFFAOYSA-N 0.000 abstract 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Dispersion Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Preparación herbicida líquida concentrada en forma de emulsión que comprende: (i) un herbicida soluble en agua, estando presente dicho herbicida en una concentración que resulta eficaz desde el punto de vista biológico cuando la preparación se diluye en un volumen de agua adecuado y se aplica al follaje de la vegetación susceptible; (ii) un herbicida soluble en aceite presente en una concentración que resulta eficaz desde el punto de vista biológico cuando la preparación se diluye en un volumen de agua adecuado y se aplica al follaje de la vegetación susceptible; (iii) uno o más cloruros solubles en agua elegidos entre el grupo que comprende: ácido clorhídrico, cloruros de metales alcalinos, cloruro de amonio, cloruros orgánicos de amonio de bajo peso molecular y cloruros de amonio cuaternario surfactantes, en una cantidad estabilizante suficiente para inhibir una degradación importante del herbicida soluble en aceite; y (iv) uno o más surfactantes presentes en una concentración suficiente para proporcionar a la emulsión una estabilidad física aceptable y para suministrarle una dispersión aceptable al diluirla en un volumen adecuado de agua para su aplicación a las plantas; donde el herbicida soluble en aceite se selecciona a partir del grupo que consta de: acetocloro, alacloro, ametrina, amidosulfuron, anilofos, atrazina, azafenidina, azimsulfuron, benfluralina, benfuresato, metil-bensulfuron, bensulida, benzfendizona, benzofenap, bromobutida, bromofenoxim, butacloro, butafenacilo, butamifos, butralina, butilato, cafenstrole, carbetamida, clorbromuron, cloridazona, etil-clorimuron, clorotoluron, clorprofam, clorsulfuron, dimetil-clortal, clortiamida, etil-cinidon, cinmetilina, cinosulfuron, clomazona, clomeprop, metil-cloransulam, cianazina, cicloato, ciclosulfamuron, daimuron, desmedifam, desmetrina, diclobenil, diflufenican, dimefuron, dimepiperato, dimetacloro, dimetametrina, dimetenamida, dinitramina, dinoterb, difenamida, ditiopir, diuron, EPTC (di-N,N-propiltiocarbamato de S-etilo), esprocarb, etalfluralina, metil-etametsulfuron, etofumesato, etoxisulfuron, etobenzanida, etil-fenoxaprop, fenuron, metil-flamprop, flazasulfuron, fluazolato, flucloralina, flumetsulam, pentil-flumiclorac, flumioxazin, fluometuron, fluorocloridona, flupoxam, flurenol, fluridona, 1-metilheptil-fluroxipir, flurtamona, metil-flutiacet, halosulfuron, hexazinona, imazosulfuron, indanofan, isoproturon, isouron, isoxaben, isoxaflutol, lenacilo, linuron, mefenacet, metamitrona, metazacloro, metabenztiazuron, metil-dimron, metobenzuron, metobromuron, metolacloro, metosulam, metoxuron, metribuzin, metsulfuron, molinato, monolinuron, naproanilida, napropamida, neburon, nicosulfuron, norflurazona, orbencarb, orizalina, oxadiargil, oxadiazon, oxasulfuron, pebulato, pendimetalina, pentanocloro, pentoxazona, fenmedifam, piperofos, pretilaclor, primisulfuron, prodiamina, profluazol, prometon, prometrina, propacloro, propanil, propazina, profam, propisocloro, propizamida, prosulfocarb, prosulfuron, etil-piraflufen, pirazogil, pirazolinato, etil-pirazosulfuron, pirazoxifen, piributicarb, piridato, metil-piriminobac, quinclorac, quinmerac, rimsulfuron, siduron, simazina, simetrina, sulcotriona, sulfentrazona, sulfometuron, sulfosulfuron, tebutam, tebuthiuron, terbacilo, terbumeton, terbutilazina, terbutrina, tenilcloro, tiazopir, tidiazimin, tifensulfuron, tiobencarb, tiocarbacil, trialato, triasulfuron, tribenuron, trietazina, trifluralina, triflusulfuron y vernolato. Un proceso para controlar el crecimiento o para eliminar la vegetación indeseable usando dicha preparación también se describe.Concentrated liquid herbicide preparation in the form of an emulsion comprising: (i) a water-soluble herbicide, said herbicide being present in a concentration that is biologically effective when the preparation is diluted in a suitable volume of water and applied to the foliage of susceptible vegetation; (ii) an oil-soluble herbicide present in a concentration that is biologically effective when the preparation is diluted in a suitable volume of water and applied to the foliage of susceptible vegetation; (iii) one or more water soluble chlorides chosen from the group comprising: hydrochloric acid, alkali metal chlorides, ammonium chloride, low molecular weight organic ammonium chlorides and surfactant quaternary ammonium chlorides, in a stabilizing amount sufficient to inhibit significant degradation of the oil soluble herbicide; and (iv) one or more surfactants present in a concentration sufficient to provide the emulsion with acceptable physical stability and to provide an acceptable dispersion by diluting it in a suitable volume of water for application to plants; where the oil-soluble herbicide is selected from the group consisting of: acetochlor, alachlor, ametrine, amidosulfuron, anilophos, atrazine, azafenidine, azimsulfuron, benfluralin, benfuresate, methyl-bensulfuron, bensulide, benzfendizona, benzofenap, bromobenzephobromaphenbromenap, bromopheaphobromophenap, bromopheaphobromophenap butachlor, butafenacil, butamifos, butraline, butylate, cafenstrole, carbetamide, chlorbromuron, chloridazone, ethyl-chlorimuron, chlorotoluron, chlorprofam, clorsulfuron, dimethyl-chlorthal, chlortiamide, ethyl-cinidon, chlo-methylpropylchine, chlo-methylpropylchine, chlo-methylpropylchine, chlo-methylpropylchine, chlo-methylpropylchine, chlo-methylpropylchine, chlo-methylpropylchine, chlo-methylpropylchine, chlo-methylpropylchine, chlo-methylpropylchine, chlormethylomethane cyanazine, cycloate, cyclosulfamuron, daimuron, desmedifam, desmethrin, diclobenyl, diflufenican, dimefuron, dimepiperate, dimetachlor, dimethamethrin, dimetenamide, dinitramine, dinoterb, diphenamide, dithiopir, diuron, EPTC (di-ethio) N-propyl di-ethyl, N-propyl N-propyl , esprocarb, etalfluralin, methyl-etametsulfuron, ethofumesate, ethoxy sulfuron, ethobenzanide, ethyl-phenoxaprop, fenuron, methyl-flamprop, flazasulfuron, fluazolate, flucloral ina, flumetsulam, pentyl flumiclorac, flumioxazin, fluometuron, fluorochloridone, flupoxam, flurenol, fluridone, 1-methylheptyl-fluroxypyr, flurtamone, methyl fluthiacet, halosulfuron, hexazinone, imazosulfuron, indanofan, isoproturon, isouron, isoxaben, isoxaflutole, lenacil, linuron, mefenacet, metamitron, metazachlor, methabenzthiazuron, methyl dymron, metobenzuron, metobromuron, metolachlor, metosulam, metoxuron, metribuzin, metsulfuron, molinate, monolinuron, naproanilide, napropamide, neburon, nicosulfuron, norflurazon, orbencarb, oryzalin, oxadiargyl, oxadiazon, oxasulfuron, pebulato, pendimethalin, pentanochloro, pentoxazone, fenmedifam, piperofos, pretilachlor, primisulfuron, prodiamine, profluazol, prometon, promethrin, propachlor, propanyl, propazine, profam, propisocloro, propizamide, pyraphoglozathroz, prosulfoglutazole pyrazogluzopropyl pyrazogluzopropyl pyrazine ethyl-pyrazulfuron, pyrazoxyfen, pyributicarb, pyridate, methyl-pyriminobac, quinclorac, quinmerac, rimsulfuron, siduron, simazin a, symmetrine, sulcotrione, sulfentrazone, sulfometuron, sulfosulfuron, tebutam, tebuthiuron, terbacillus, terbumeton, terbutylazine, terbutrine, tenylchloro, thiazopyr, tidiazimin, tifensulfuron, thiobencarb, triathlonol, triathlonol, triathlonol, triathlonol, triathlonol, triathlonol, triathlonol, triathlonol, triathlonol, triathlonol A process to control growth or to eliminate undesirable vegetation using such preparation is also described.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US33134801P | 2001-02-14 | 2001-02-14 | |
| US26919301P | 2001-02-15 | 2001-02-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR035747A1 true AR035747A1 (en) | 2004-07-07 |
Family
ID=26953559
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP020100502A AR032691A1 (en) | 2001-02-14 | 2002-02-14 | COFORMULATION OF ETIL-CARFENTRAZONA AND A WATER SOLUBLE HERBICIDE |
| ARP020100503A AR035747A1 (en) | 2001-02-14 | 2002-02-14 | HERBICIDE PREPARATION LIQUID CONCENTRATED IN THE FORM OF EMULSION AND PROCESS TO CONTROL GROWTH OR TO ELIMINATE INDESEABLE VEGETATION |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP020100502A AR032691A1 (en) | 2001-02-14 | 2002-02-14 | COFORMULATION OF ETIL-CARFENTRAZONA AND A WATER SOLUBLE HERBICIDE |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP1359800A2 (en) |
| CN (1) | CN1514686A (en) |
| AR (2) | AR032691A1 (en) |
| AU (1) | AU2002245479A1 (en) |
| BR (1) | BR0207259A (en) |
| CA (1) | CA2437741A1 (en) |
| CZ (1) | CZ20032183A3 (en) |
| HU (1) | HUP0303734A2 (en) |
| MX (2) | MX237457B (en) |
| PL (1) | PL364247A1 (en) |
| RU (1) | RU2003127742A (en) |
| WO (2) | WO2002078442A2 (en) |
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| ES2364149T3 (en) | 2004-03-12 | 2011-08-25 | Fmc Corporation | COMPOSITION OF GLYPHOSATE. |
| GB0601304D0 (en) * | 2006-01-23 | 2006-03-01 | Syngenta Ltd | Herbicide formulation |
| EP1925203A1 (en) * | 2006-11-13 | 2008-05-28 | Bayer CropScience AG | Herbicidal combinations comprising amidosulfuron and a pyridine-herbicide |
| PL2094083T3 (en) | 2006-12-06 | 2015-03-31 | Akzo Nobel Chemicals Int Bv | Alkylamidopropyl dialkylamine surfactants as adjuvants |
| ES2636918T3 (en) | 2006-12-06 | 2017-10-10 | Akzo Nobel N.V. | Compatibility agents for herbicidal formulations comprising salts of 2,4- (dichlorophenoxy) acetic acid |
| CN101371660B (en) * | 2008-06-27 | 2011-06-15 | 甘肃省农业科学院农产品贮藏加工研究所 | Sprouting inhibition agent emulsifiable solution for white potato |
| CN101455201A (en) * | 2009-01-14 | 2009-06-17 | 安徽华星化工股份有限公司 | Composition for controlling broad leaved weed in wheat field |
| CN101485315A (en) * | 2009-02-13 | 2009-07-22 | 安徽华星化工股份有限公司 | Cornfield herbicidal composition containing benazolin |
| US8815773B2 (en) * | 2009-07-29 | 2014-08-26 | Upl Limited | Herbicidal combination |
| CN102027931B (en) * | 2009-09-28 | 2013-09-18 | 南京华洲药业有限公司 | Synergistic herbicide composition containing triclopyr and hexazinone and application thereof |
| CN102027913B (en) * | 2009-09-28 | 2013-09-18 | 南京华洲药业有限公司 | Herbicide composition containing dithiopyr and triclopyr and application thereof |
| CN102027915B (en) * | 2009-09-28 | 2013-09-18 | 南京华洲药业有限公司 | Herbicidal composition containing dithiopyr and picloram and application thereof |
| CN102027974B (en) * | 2009-09-28 | 2013-09-18 | 南京华洲药业有限公司 | Herbicidal composition containing rimsulfuron and 2,4-dichlorphenoxyacetic-acid and application thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1990007277A1 (en) * | 1988-12-27 | 1990-07-12 | Monsanto Company | Compositions containing a polar and a nonpolar herbicide |
| EP0617894B1 (en) * | 1993-04-02 | 1998-12-16 | Monsanto Europe S.A./N.V. | Liquid concentrated herbicidal glyphosate compositions |
| JPH0789817A (en) * | 1993-09-17 | 1995-04-04 | Nippon Soda Co Ltd | Aqueous dispersion type herbicide |
| JP3799669B2 (en) * | 1996-07-29 | 2006-07-19 | 日産化学工業株式会社 | Herbicidal composition |
| US6127318A (en) * | 1998-04-03 | 2000-10-03 | Monsanto Company | Combination of glyphosate and a triazolinone herbicide |
-
2002
- 2002-02-14 CA CA002437741A patent/CA2437741A1/en not_active Abandoned
- 2002-02-14 PL PL02364247A patent/PL364247A1/en unknown
- 2002-02-14 CN CNA02806710XA patent/CN1514686A/en active Pending
- 2002-02-14 MX MXPA03007371 patent/MX237457B/en active IP Right Grant
- 2002-02-14 EP EP02728358A patent/EP1359800A2/en not_active Withdrawn
- 2002-02-14 MX MXPA03007280A patent/MXPA03007280A/en unknown
- 2002-02-14 RU RU2003127742/15A patent/RU2003127742A/en not_active Application Discontinuation
- 2002-02-14 HU HU0303734A patent/HUP0303734A2/en unknown
- 2002-02-14 AR ARP020100502A patent/AR032691A1/en unknown
- 2002-02-14 WO PCT/US2002/005734 patent/WO2002078442A2/en not_active Application Discontinuation
- 2002-02-14 AU AU2002245479A patent/AU2002245479A1/en not_active Abandoned
- 2002-02-14 BR BR0207259-9A patent/BR0207259A/en not_active Application Discontinuation
- 2002-02-14 AR ARP020100503A patent/AR035747A1/en unknown
- 2002-02-14 CZ CZ20032183A patent/CZ20032183A3/en unknown
- 2002-02-14 WO PCT/US2002/005144 patent/WO2002063955A2/en not_active Application Discontinuation
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| MXPA03007371A (en) | 2003-12-04 |
| WO2002078442A2 (en) | 2002-10-10 |
| CZ20032183A3 (en) | 2004-02-18 |
| AR032691A1 (en) | 2003-11-19 |
| CA2437741A1 (en) | 2002-10-10 |
| AU2002245479A1 (en) | 2002-08-28 |
| MXPA03007280A (en) | 2003-12-04 |
| EP1359800A2 (en) | 2003-11-12 |
| WO2002078442A3 (en) | 2003-01-03 |
| PL364247A1 (en) | 2004-12-13 |
| CN1514686A (en) | 2004-07-21 |
| WO2002063955A3 (en) | 2003-03-20 |
| RU2003127742A (en) | 2005-03-10 |
| MX237457B (en) | 2006-06-02 |
| BR0207259A (en) | 2004-02-10 |
| WO2002063955A2 (en) | 2002-08-22 |
| HUP0303734A2 (en) | 2004-03-29 |
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