RU2001107014A - HERBICIDAL PRODUCTS FOR TOLERANT OR RESISTANT GRAIN CROPS - Google Patents
HERBICIDAL PRODUCTS FOR TOLERANT OR RESISTANT GRAIN CROPSInfo
- Publication number
- RU2001107014A RU2001107014A RU2001107014/04A RU2001107014A RU2001107014A RU 2001107014 A RU2001107014 A RU 2001107014A RU 2001107014/04 A RU2001107014/04 A RU 2001107014/04A RU 2001107014 A RU2001107014 A RU 2001107014A RU 2001107014 A RU2001107014 A RU 2001107014A
- Authority
- RU
- Russia
- Prior art keywords
- herbicides
- group
- action
- combination
- crops
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title claims 3
- 239000004009 herbicide Substances 0.000 claims 22
- 241000196324 Embryophyta Species 0.000 claims 16
- 239000003112 inhibitor Substances 0.000 claims 9
- -1 fenoxaprop-R Chemical compound 0.000 claims 7
- 239000000203 mixture Substances 0.000 claims 7
- 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 5
- 108020001991 Protoporphyrinogen Oxidase Proteins 0.000 claims 5
- 239000013543 active substance Substances 0.000 claims 5
- 235000013339 cereals Nutrition 0.000 claims 5
- 102100029028 Protoporphyrinogen oxidase Human genes 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 claims 4
- 239000002689 soil Substances 0.000 claims 4
- 230000000694 effects Effects 0.000 claims 3
- 230000035784 germination Effects 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- RBSXHDIPCIWOMG-UHFFFAOYSA-N 1-(4,6-dimethoxypyrimidin-2-yl)-3-(2-ethylsulfonylimidazo[1,2-a]pyridin-3-yl)sulfonylurea Chemical compound CCS(=O)(=O)C=1N=C2C=CC=CN2C=1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 RBSXHDIPCIWOMG-UHFFFAOYSA-N 0.000 claims 2
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 claims 2
- 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 claims 2
- 239000002890 Aclonifen Substances 0.000 claims 2
- 239000005476 Bentazone Substances 0.000 claims 2
- 239000005484 Bifenox Substances 0.000 claims 2
- 239000005489 Bromoxynil Substances 0.000 claims 2
- 239000005492 Carfentrazone-ethyl Substances 0.000 claims 2
- 239000005494 Chlorotoluron Substances 0.000 claims 2
- 239000005499 Clomazone Substances 0.000 claims 2
- 239000005507 Diflufenican Substances 0.000 claims 2
- 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 claims 2
- 239000005558 Fluroxypyr Substances 0.000 claims 2
- 239000005562 Glyphosate Substances 0.000 claims 2
- 239000005568 Iodosulfuron Substances 0.000 claims 2
- SUSRORUBZHMPCO-UHFFFAOYSA-N MC-4379 Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC)=CC(OC=2C(=CC(Cl)=CC=2)Cl)=C1 SUSRORUBZHMPCO-UHFFFAOYSA-N 0.000 claims 2
- 239000005578 Mesotrione Substances 0.000 claims 2
- 239000005582 Metosulam Substances 0.000 claims 2
- 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 claims 2
- 239000005583 Metribuzin Substances 0.000 claims 2
- 239000005591 Pendimethalin Substances 0.000 claims 2
- 239000005595 Picloram Substances 0.000 claims 2
- 239000005603 Prosulfocarb Substances 0.000 claims 2
- 239000005618 Sulcotrione Substances 0.000 claims 2
- 239000005619 Sulfosulfuron Substances 0.000 claims 2
- DDBMQDADIHOWIC-UHFFFAOYSA-N aclonifen Chemical compound C1=C([N+]([O-])=O)C(N)=C(Cl)C(OC=2C=CC=CC=2)=C1 DDBMQDADIHOWIC-UHFFFAOYSA-N 0.000 claims 2
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 claims 2
- CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzidamine Natural products C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 claims 2
- JXCGFZXSOMJFOA-UHFFFAOYSA-N chlorotoluron Chemical compound CN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 JXCGFZXSOMJFOA-UHFFFAOYSA-N 0.000 claims 2
- KIEDNEWSYUYDSN-UHFFFAOYSA-N clomazone Chemical compound O=C1C(C)(C)CON1CC1=CC=CC=C1Cl KIEDNEWSYUYDSN-UHFFFAOYSA-N 0.000 claims 2
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 claims 2
- WYEHFWKAOXOVJD-UHFFFAOYSA-N diflufenican Chemical compound FC1=CC(F)=CC=C1NC(=O)C1=CC=CN=C1OC1=CC=CC(C(F)(F)F)=C1 WYEHFWKAOXOVJD-UHFFFAOYSA-N 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- MLKCGVHIFJBRCD-UHFFFAOYSA-N ethyl 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoate Chemical group C1=C(Cl)C(CC(Cl)C(=O)OCC)=CC(N2C(N(C(F)F)C(C)=N2)=O)=C1F MLKCGVHIFJBRCD-UHFFFAOYSA-N 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 claims 2
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims 2
- 229940097068 glyphosate Drugs 0.000 claims 2
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 claims 2
- FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 claims 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 2
- 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 claims 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims 2
- 230000029553 photosynthesis Effects 0.000 claims 2
- 238000010672 photosynthesis Methods 0.000 claims 2
- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 claims 2
- 239000004476 plant protection product Substances 0.000 claims 2
- NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 claims 2
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 claims 2
- 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 2
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims 1
- HWNPEODOOZPOKQ-UHFFFAOYSA-N 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-4-(methanesulfonamidomethyl)-3-methylbenzoic acid Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(CNS(C)(=O)=O)C=2C)C(O)=O)=N1 HWNPEODOOZPOKQ-UHFFFAOYSA-N 0.000 claims 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 claims 1
- OOLBCHYXZDXLDS-UHFFFAOYSA-N 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(Cl)C=C1Cl OOLBCHYXZDXLDS-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- 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 1
- ZBMRKNMTMPPMMK-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid;azane Chemical compound [NH4+].CP(O)(=O)CCC(N)C([O-])=O ZBMRKNMTMPPMMK-UHFFFAOYSA-N 0.000 claims 1
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 claims 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 claims 1
- 239000003666 Amidosulfuron Substances 0.000 claims 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 claims 1
- 239000005498 Clodinafop Substances 0.000 claims 1
- 239000005500 Clopyralid Substances 0.000 claims 1
- 229920000742 Cotton Polymers 0.000 claims 1
- 239000005504 Dicamba Substances 0.000 claims 1
- 239000005506 Diclofop Substances 0.000 claims 1
- 239000005559 Flurtamone Substances 0.000 claims 1
- 239000005561 Glufosinate Substances 0.000 claims 1
- 239000005574 MCPA Substances 0.000 claims 1
- 239000005604 Prosulfuron Substances 0.000 claims 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 claims 1
- 102000005135 Protoporphyrinogen oxidase Human genes 0.000 claims 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims 1
- 239000005626 Tribenuron Substances 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 239000012752 auxiliary agent Substances 0.000 claims 1
- 150000003851 azoles Chemical class 0.000 claims 1
- ZEKANFGSDXODPD-UHFFFAOYSA-O carboxymethyl(phosphonomethyl)azanium;propan-2-amine Chemical compound CC(C)[NH3+].OC(=O)CNCP(O)(O)=O ZEKANFGSDXODPD-UHFFFAOYSA-O 0.000 claims 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 claims 1
- 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 1
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- WXUNXXKSYBUHMK-UHFFFAOYSA-N methyl 4-methyl-2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)benzoate;methyl 5-methyl-2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)benzoate Chemical compound COC(=O)C1=CC=C(C)C=C1C1=NC(C)(C(C)C)C(=O)N1.COC(=O)C1=CC(C)=CC=C1C1=NC(C)(C(C)C)C(=O)N1 WXUNXXKSYBUHMK-UHFFFAOYSA-N 0.000 claims 1
- 150000004702 methyl esters Chemical class 0.000 claims 1
- 108090000765 processed proteins & peptides Proteins 0.000 claims 1
- YXIIPOGUBVYZIW-UHFFFAOYSA-N pyraflufen Chemical compound ClC1=C(OC(F)F)N(C)N=C1C1=CC(OCC(O)=O)=C(Cl)C=C1F YXIIPOGUBVYZIW-UHFFFAOYSA-N 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 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 claims 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 claims 1
- 0 C=*CNCC(C1)(C1O)O Chemical compound C=*CNCC(C1)(C1O)O 0.000 description 1
Claims (9)
где Z означает остаток формулы -ОН или пептидный остаток формулы -NHСH(СН3)СОNНСН(СН3)СООН или -NHСH(СН3)СОNНСН[СН2СН(СН3)2] СООН,
и их эфиров и солей и других производных фосфинотрицина, (А2) соединений формулы (А2) и их эфиров и солей,
(A3) имидазолинонов и их солей и (А4) гербицидных азолов из группы ингибиторов протопорфириноген-оксидазы (РРО-ингибиторы) и РРО-ингибиторов WC9717, и (В) одного или нескольких гербицидов из группы соединений, которая состоит из (B1) гербицидов, действующих селективно в зерновых культурах, особенно против однодольных сорных растений, с действием на листву и/или с действием на почву (остаточное действие) из группы изопротурона, хлоротолурона, флутиамида просульфокарба, пендиметалина, феноксапропа-Р, феноксапропа, клодинафопа, диклофопа, тралкоксидима, имазаметабенза и флупирсульфурона, (B2) гербицидов, действующих селективно в зерновых культурах против однодольных и двудольных сорных растений, с преимущественным действием на листву из группы метсульфурона, триасульфурона, AEF060, иодосульфурона, хлорсульфурона и сульфосульфурона, или (B3) гербицидов, действующих селективно в зерновых культурах против однодольных и двудольных сорных растений, с действием на листву и на почву из группы дифлуфеникана/флуртамона, метосулама и флуметсулама и (B4) гербицидов, действующих селективно в зерновых культурах против однодольных и двудольных сорняков, с действием на листву из группы (B4.1) трибенурона, амидосульфурона, LAB271272, тифенсульфурона, просульфурона и цинидон-этила и (B4.2) типа останавливающих рост гербицидов из группы 2,4-D, СМРР-Р, дихлорпропа, МСРА, флуроксипира, дикамба, пикло-рама, бентазона и клопиралида и (B4.3) гидроксибензонитрилов/(ингибиторов фотосинтеза) из группы бромоксинила, иоксинила, бифенокса и метрибузина или (B4.4) РРО-ингибиторов из группы карфентразона, пирафлуфена и флуорогликофена или (B4.5) HPPDO-ингибиторов, которые отличны от активного вещества (А), содержащегося соответственно в некоторых случаях в составе, из группы пиклонифена, аклонифена, изоксафлутола, кломазона, сулкотриона и мезотриона, и зерновые культуры толерантны по отношению к содержащимся в комбинации гербицидам (А) и (В), при необходимости, в присутствии веществ, способствующих сохранности, исключая применение комбинаций гербицидов, которые содержат (а) комбинацию (В) метилового эфира 4-метилсульфониламинометил-2-(4,6-диметоксипиримидин-2-илкарбамоилсульфамоил)бензойной кислоты (AEF060) и (А1) глюфосината или (А2) глифосата, или (A3) имазаметабенза, или (А4) карфентразона(-этил), или (b) комбинацию (А4) карфентразон-этила и изопротурона или трибенурон-метила.1. The use of a combination of herbicides for controlling weeds in cotton crops, characterized in that the corresponding combination of herbicides contains the following synergistically active components: (A) one or more broad-spectrum herbicides from the group of compounds, which consists of (A1) compounds of the formulas ( A1)
where Z is a residue of the formula —OH or a peptide residue of the formula —NHCH (CH 3 ) CONCHCH (CH 3 ) COOH or —NHCH (CH 3 ) CONCHCH [CH 2 CH (CH 3 ) 2 ] COOH,
and their esters and salts and other derivatives of phosphinotricin, (A2) compounds of formula (A2) and their esters and salts,
(A3) imidazolinones and their salts; and (A4) herbicidal azoles from the group of protoporphyrinogen oxidase inhibitors (PPO inhibitors) and PPO inhibitors WC9717, and (B) one or more herbicides from the group of compounds that consists of (B1) herbicides, acting selectively in crops, especially against monocotyledonous weeds, with action on foliage and / or with action on the soil (residual effect) from the group of isoproturon, chlorotoluron, flutiamide prosulfocarb, pendimethalin, fenoxaprop-R, fenoxaprop, clodinafop, diclofopl, tral ima, imazametabenz and flupirsulfuron, (B2) herbicides that act selectively in crops against monocotyledonous and dicotyledonous weeds, with a predominant effect on foliage from the group of metsulfuron, triasulfuron, AEF060, iodosulfuron, chlorosulfuron and sulfosulfuron, or (B3) in cereals against monocotyledonous and dicotyledonous weeds, with action on foliage and soil from the group of diflufenican / flurtamon, metosulam and flumetsulam and (B4) herbicides acting selectively in grains cultures against monocotyledonous and dicotyledonous weeds, with the action of foliage from the group (B4.1) of tribenuron, amidosulfuron, LAB271272, tifensulfuron, prosulfuron and cinidone-ethyl and (B4.2) type of growth-arresting herbicides from the 2,4-D group, CMPP-P, dichloroprop, MCPA, fluroxypyr, dicamba, picloram, bentazone and clopyralide and (B4.3) hydroxybenzonitriles / (photosynthesis inhibitors) from the group of bromoxynil, ioxynil, bifenox and metribuzin or (B4.4) PPO inhibitors groups of carfentrazone, piraflufen and fluoroglycophene or (B4.5) HPPDO inhibitors, which are different from the active substance (A), which is respectively contained in some cases in the composition, from the group of piklonifen, aclonifen, isoxaflutol, clomazone, sulcotrione and mesotrione, and crops are tolerant to the herbicides (A) and (B) contained in the combination, if necessary, in the presence of preserving substances, excluding the use of combinations of herbicides that contain (a) a combination of (B) methyl 4-methylsulfonylaminomethyl-2- (4,6-dimethoxypyrimidin-2-ylcarbamoylsulfamoyl) benzoic acid (AEF060) and (A1 ) lyufosinata or (A2) glyphosate, or (A3) imazamethabenz, or (A4) carfentrazone (-ethyl), or (b) the combination of (A4) carfentrazone-ethyl, isoproturon or tribenuron-methyl.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19836700.7 | 1998-08-13 | ||
| DE19836700A DE19836700A1 (en) | 1998-08-13 | 1998-08-13 | Use of a synergistic herbicide combination including a glufosinate- or glyphosate-type, imidazolinone or protoporphyrinogen oxidase inhibitory azole herbicide to control weeds in cereals |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2001107014A true RU2001107014A (en) | 2003-02-10 |
| RU2250614C2 RU2250614C2 (en) | 2005-04-27 |
Family
ID=7877416
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2001107014/04A RU2250614C2 (en) | 1998-08-13 | 1999-08-10 | Herbicides for tolerant or resistant grain crops, method for controlling of weeds |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US6723681B2 (en) |
| EP (1) | EP1104992B2 (en) |
| JP (1) | JP2002522460A (en) |
| KR (2) | KR20010087182A (en) |
| CN (1) | CN1220437C (en) |
| AR (2) | AR020162A1 (en) |
| AT (1) | ATE290317T1 (en) |
| AU (1) | AU767032B2 (en) |
| BR (1) | BR9913006A (en) |
| CA (4) | CA2340193C (en) |
| CZ (1) | CZ304256B6 (en) |
| DE (2) | DE19836700A1 (en) |
| ES (1) | ES2239850T5 (en) |
| HU (1) | HU230431B1 (en) |
| IL (1) | IL141144A (en) |
| NZ (1) | NZ509845A (en) |
| PL (24) | PL217912B1 (en) |
| PT (1) | PT1104992E (en) |
| RU (1) | RU2250614C2 (en) |
| SK (1) | SK288448B6 (en) |
| TR (1) | TR200100479T2 (en) |
| UA (1) | UA71569C2 (en) |
| WO (1) | WO2000008940A1 (en) |
| ZA (1) | ZA200101142B (en) |
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| US7577151B2 (en) * | 2005-04-01 | 2009-08-18 | International Business Machines Corporation | Method and apparatus for providing a network connection table |
| US7508771B2 (en) * | 2005-04-01 | 2009-03-24 | International Business Machines Corporation | Method for reducing latency in a host ethernet adapter (HEA) |
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| EP2252146A2 (en) * | 2008-02-05 | 2010-11-24 | Arysta LifeScience North America, LLC | Solid formulation of low melting active compound |
| RU2364601C1 (en) * | 2008-04-21 | 2009-08-20 | Государственное учреждение "Научно-исследовательский технологический институт гербицидов и регуляторов роста растений с опытно-экспериментальным производством Академии наук Республики Башкортостан" | Method of obtaining alkali metal salts of n-phosphonomethylglycine |
| RU2395203C1 (en) * | 2009-01-21 | 2010-07-27 | Государственное учреждение "Научно-исследовательский технологический институт гербицидов и регуляторов роста растений с опытно-экспериментальным производством Академии наук Республики Башкортостан" | Herbicide composition |
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-
1998
- 1998-08-13 DE DE19836700A patent/DE19836700A1/en not_active Withdrawn
-
1999
- 1999-08-10 US US09/371,770 patent/US6723681B2/en not_active Expired - Lifetime
- 1999-08-10 KR KR1020017001848A patent/KR20010087182A/en not_active Ceased
- 1999-08-10 PL PL401505A patent/PL217912B1/en unknown
- 1999-08-10 BR BR9913006-8A patent/BR9913006A/en not_active IP Right Cessation
- 1999-08-10 PL PL397711A patent/PL217247B1/en unknown
- 1999-08-10 ES ES99941559T patent/ES2239850T5/en not_active Expired - Lifetime
- 1999-08-10 PL PL401515A patent/PL218895B1/en unknown
- 1999-08-10 PL PL401517A patent/PL217917B1/en unknown
- 1999-08-10 PL PL401513A patent/PL218894B1/en unknown
- 1999-08-10 PL PL387554A patent/PL218886B1/en unknown
- 1999-08-10 PL PL401506A patent/PL218242B1/en unknown
- 1999-08-10 PL PL397706A patent/PL217209B1/en unknown
- 1999-08-10 PL PL401514A patent/PL219930B1/en unknown
- 1999-08-10 CA CA2340193A patent/CA2340193C/en not_active Expired - Lifetime
- 1999-08-10 PL PL401510A patent/PL218213B1/en unknown
- 1999-08-10 KR KR1020087014141A patent/KR20080059342A/en not_active Ceased
- 1999-08-10 PL PL401509A patent/PL219915B1/en unknown
- 1999-08-10 PL PL397712A patent/PL217235B1/en unknown
- 1999-08-10 PT PT99941559T patent/PT1104992E/en unknown
- 1999-08-10 DE DE59911735T patent/DE59911735D1/en not_active Expired - Lifetime
- 1999-08-10 PL PL401518A patent/PL218249B1/en unknown
- 1999-08-10 CA CA2936388A patent/CA2936388C/en not_active Expired - Lifetime
- 1999-08-10 CA CA2793821A patent/CA2793821C/en not_active Expired - Lifetime
- 1999-08-10 PL PL401516A patent/PL218880B1/en unknown
- 1999-08-10 HU HU0103462A patent/HU230431B1/en unknown
- 1999-08-10 PL PL397705A patent/PL217213B1/en unknown
- 1999-08-10 PL PL397713A patent/PL217230B1/en unknown
- 1999-08-10 NZ NZ509845A patent/NZ509845A/en unknown
- 1999-08-10 JP JP2000564454A patent/JP2002522460A/en not_active Abandoned
- 1999-08-10 TR TR2001/00479T patent/TR200100479T2/en unknown
- 1999-08-10 PL PL397714A patent/PL217241B1/en unknown
- 1999-08-10 RU RU2001107014/04A patent/RU2250614C2/en active
- 1999-08-10 PL PL397709A patent/PL217214B1/en unknown
- 1999-08-10 PL PL393881A patent/PL215351B1/en unknown
- 1999-08-10 PL PL346124A patent/PL212668B1/en unknown
- 1999-08-10 SK SK213-2001A patent/SK288448B6/en not_active IP Right Cessation
- 1999-08-10 EP EP99941559A patent/EP1104992B2/en not_active Expired - Lifetime
- 1999-08-10 PL PL401512A patent/PL218250B1/en unknown
- 1999-08-10 AT AT99941559T patent/ATE290317T1/en not_active IP Right Cessation
- 1999-08-10 IL IL14114499A patent/IL141144A/en not_active IP Right Cessation
- 1999-08-10 CN CNB998096164A patent/CN1220437C/en not_active Expired - Lifetime
- 1999-08-10 CA CA2794516A patent/CA2794516C/en not_active Expired - Lifetime
- 1999-08-10 PL PL397710A patent/PL217250B1/en unknown
- 1999-08-10 PL PL401511A patent/PL218251B1/en unknown
- 1999-08-10 WO PCT/EP1999/005801 patent/WO2000008940A1/en not_active Ceased
- 1999-08-10 AU AU55128/99A patent/AU767032B2/en not_active Expired
- 1999-08-10 PL PL401504A patent/PL217911B1/en unknown
- 1999-08-10 CZ CZ2001-555A patent/CZ304256B6/en not_active IP Right Cessation
- 1999-08-11 AR ARP990104016A patent/AR020162A1/en active IP Right Grant
- 1999-10-08 UA UA2001031685A patent/UA71569C2/en unknown
-
2001
- 2001-02-09 ZA ZA200101142A patent/ZA200101142B/en unknown
-
2013
- 2013-02-07 AR ARP130100384A patent/AR089930A2/en not_active Application Discontinuation
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