AR099865A1 - METHODS FOR SELECTLY CONTROLLING PLANTS USING COMPOSITIONS CONTAINING PHOTOSYSTEM II INHIBITORS AND OXIDASE PROTOPORPHYRINOGEN INHIBITORS - Google Patents
METHODS FOR SELECTLY CONTROLLING PLANTS USING COMPOSITIONS CONTAINING PHOTOSYSTEM II INHIBITORS AND OXIDASE PROTOPORPHYRINOGEN INHIBITORSInfo
- Publication number
- AR099865A1 AR099865A1 ARP150100913A ARP150100913A AR099865A1 AR 099865 A1 AR099865 A1 AR 099865A1 AR P150100913 A ARP150100913 A AR P150100913A AR P150100913 A ARP150100913 A AR P150100913A AR 099865 A1 AR099865 A1 AR 099865A1
- Authority
- AR
- Argentina
- Prior art keywords
- butamethylthio
- butanedinyl
- ethyl
- photosystem
- inhibitor
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 8
- 239000000203 mixture Substances 0.000 title abstract 7
- 108010060806 Photosystem II Protein Complex Proteins 0.000 title abstract 6
- 102000004316 Oxidoreductases Human genes 0.000 title 1
- 108090000854 Oxidoreductases Proteins 0.000 title 1
- UHSGPDMIQQYNAX-UHFFFAOYSA-N protoporphyrinogen Chemical compound C1C(=C(C=2C=C)C)NC=2CC(=C(C=2CCC(O)=O)C)NC=2CC(N2)=C(CCC(O)=O)C(C)=C2CC2=C(C)C(C=C)=C1N2 UHSGPDMIQQYNAX-UHFFFAOYSA-N 0.000 title 1
- 244000286177 Raphanus raphanistrum Species 0.000 abstract 5
- FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 abstract 5
- 235000013339 cereals Nutrition 0.000 abstract 4
- MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 abstract 4
- 241000219193 Brassicaceae Species 0.000 abstract 3
- 239000005492 Carfentrazone-ethyl Substances 0.000 abstract 3
- 229940087098 Oxidase inhibitor Drugs 0.000 abstract 3
- 108020001991 Protoporphyrinogen Oxidase Proteins 0.000 abstract 3
- 102000005135 Protoporphyrinogen oxidase Human genes 0.000 abstract 3
- SNCZNSNPXMPCGN-UHFFFAOYSA-N butanediamide Chemical compound NC(=O)CCC(N)=O SNCZNSNPXMPCGN-UHFFFAOYSA-N 0.000 abstract 3
- 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 abstract 3
- 241000196324 Embryophyta Species 0.000 abstract 2
- CAWXEEYDBZRFPE-UHFFFAOYSA-N Hexazinone Chemical compound O=C1N(C)C(N(C)C)=NC(=O)N1C1CCCCC1 CAWXEEYDBZRFPE-UHFFFAOYSA-N 0.000 abstract 2
- 235000000241 Raphanus raphanistrum Nutrition 0.000 abstract 2
- RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical group CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 abstract 2
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 abstract 2
- 230000002363 herbicidal effect Effects 0.000 abstract 2
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 abstract 2
- MVHWKYHDYCGNQN-UHFFFAOYSA-N 1,5-dichloro-3-fluoro-2-(4-nitrophenoxy)benzene Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=C(F)C=C(Cl)C=C1Cl MVHWKYHDYCGNQN-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
- 239000005484 Bifenox Substances 0.000 abstract 1
- IRECWLYBCAZIJM-UHFFFAOYSA-N Flumiclorac pentyl Chemical group C1=C(Cl)C(OCC(=O)OCCCCC)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1F IRECWLYBCAZIJM-UHFFFAOYSA-N 0.000 abstract 1
- 239000005532 Flumioxazine Substances 0.000 abstract 1
- 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 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
- NNKKTZOEKDFTBU-YBEGLDIGSA-N cinidon ethyl Chemical compound C1=C(Cl)C(/C=C(\Cl)C(=O)OCC)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1 NNKKTZOEKDFTBU-YBEGLDIGSA-N 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- DNUAYCRATWAJQE-UHFFFAOYSA-N flufenpyr-ethyl Chemical group C1=C(Cl)C(OCC(=O)OCC)=CC(N2C(C(C)=C(C=N2)C(F)(F)F)=O)=C1F DNUAYCRATWAJQE-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- CONWAEURSVPLRM-UHFFFAOYSA-N lactofen Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC(C)C(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 CONWAEURSVPLRM-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
- XITQUSLLOSKDTB-UHFFFAOYSA-N nitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(Cl)C=C1Cl XITQUSLLOSKDTB-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
- 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
- RVULBHWZFCBODE-UHFFFAOYSA-M sodium;5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate Chemical group [Na+].C1=C([N+]([O-])=O)C(C(=O)[O-])=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 RVULBHWZFCBODE-UHFFFAOYSA-M 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
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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/707—1,2,3- or 1,2,4-triazines; Hydrogenated 1,2,3- or 1,2,4-triazines
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Catching Or Destruction (AREA)
Abstract
Reivindicación 1: Un método para el control selectivo de una planta de la familia Brassicaceae en un cultivo de cereal, que comprende aplicar a dicha planta Brassicaceae una cantidad efectiva herbicida de una composición que comprende (a) un inhibidor de fotosistema II y (b) un inhibidor de protoporfirinógeno oxidasa. Reivindicación 6: El método de la reivindicación 1, en donde el inhibidor de fotosistema II se selecciona del grupo que consiste en ametrina, atrazina, cianazina, hexazinona, metribuzina y simazina. Reivindicación 7: El método de la reivindicación 6, en donde el inhibidor de fotosistema II es metribuzina. Reivindicación 8: El método de la reivindicación 1, en donde el inhibidor de protoporfirinógeno oxidasa se selecciona del grupo que consiste en acifluorfeno de sodio, bifenox, clometoxifeno, clornitrofeno, etoxifeno etilo, fluorodifeno, fluoroglicofeno-etilo, fluoronitrofeno, fomesafeno, furiloxifeno, halosafeno, lactofeno, nitrofeno, nitrofluorfeno, oxifluorfeno, cinidon-etilo, flumiclorac-pentilo, flumioxazina, profluazol, pirazogilo, oxadiargilo, oxadiazon, pentoxazona, fluazolato, piraflufeno-etilo, benzfendizona, butafenacil, flutiacet-metilo, tidiazimin, azafenidin, carfentrazona-etilo, sulfentrazona y flufenpir-etilo. Reivindicación 9: El método de la reivindicación 8, en donde el inhibidor de protoporfirinógeno oxidasa es carfentrazona-etilo. Reivindicación 10: El método de la reivindicación 1, en donde la planta de la familia Brassicaceae comprende Raphanus raphanistrum. Reivindicación 11: Un método para el control selectivo de la planta Raphanus raphanistrum en un cultivo de cereal, que comprende aplicar a dicho Raphanus raphanistrum una cantidad efectiva herbicida de una composición que comprende (a) metribuzina y (b) carfentrazona-etilo. Reivindicación 15: Una composición para controlar en forma selectiva la planta Raphanus raphanistrum en un cultivo de cereal, dicha composición comprende carfentrazona-etilo y un inhibidor de fotosistema II en una relación de 1:4 a 1:20 en peso, que controla selectivamente la planta Raphanus raphanistrum en un cultivo de cereal. Reivindicación 16: La composición de la reivindicación 15, en donde el inhibidor de fotosistema II se selecciona del grupo que consiste en ametrina, atrazina, cianazina, hexazinona, metribuzina y simazina. Reivindicación 17: La composición de la reivindicación 16, en donde el inhibidor de fotosistema II es metribuzina.Claim 1: A method for the selective control of a plant of the Brassicaceae family in a cereal crop, which comprises applying to said Brassicaceae plant an effective herbicidal amount of a composition comprising (a) a photosystem II inhibitor and (b) a protoporphyrinogen oxidase inhibitor. Claim 6: The method of claim 1, wherein the photosystem II inhibitor is selected from the group consisting of ametrine, atrazine, cyanazine, hexazinone, metribuzine and simazine. Claim 7: The method of claim 6, wherein the photosystem II inhibitor is metribuzine. Claim 8: The method of claim 1, wherein the protoporphyrinogen oxidase inhibitor is selected from the group consisting of sodium acifluorfen, bifenox, clomethoxyphene, clornitrophene, ethoxyphene ethyl, fluorodiphene, fluoroglyphene-ethyl, fluoronitrofen, phomesaphene, furiloxenphene, furiloxenphene, furiloxenphene , lactofen, nitrofen, nitrofluorphene, oxyfluorphene, cinidon-ethyl, flumiclorac-pentyl, flumioxazine, profluazol, pyrazogyl, oxadiargyl, oxadiazon, pentoxazone, fluazolate, pyrafluphene-ethyl, benzfenedinyl, butaphenylethyl, butamethylthio, butamethylthio, butamethylthio, butanediamide, butamethylthio, butamethylthio, butamethylthio, butamethylthio, butamethylthio, butamethylthio, butamethylthio, butanedinyl, butaphenylone, butamethylthio, butamethylthio, butamethylthio, butanediamide, butanedinyl, butanedinyl, butanedinyl, butanedinyl, butanedinyl, butanedinyl, butanedinyl, butanedinyl, butanedinyl, butanedinyl, butanedinyl, butanediamide , sulfentrazone and flufenpyr-ethyl. Claim 9: The method of claim 8, wherein the protoporphyrinogen oxidase inhibitor is carfentrazone-ethyl. Claim 10: The method of claim 1, wherein the plant of the Brassicaceae family comprises Raphanus raphanistrum. Claim 11: A method for the selective control of the Raphanus raphanistrum plant in a cereal crop, comprising applying to said Raphanus raphanistrum an effective herbicidal amount of a composition comprising (a) metribuzine and (b) carfentrazone-ethyl. Claim 15: A composition for selectively controlling the Raphanus raphanistrum plant in a cereal crop, said composition comprises carfentrazone-ethyl and a photosystem II inhibitor in a ratio of 1: 4 to 1:20 by weight, which selectively controls the Raphanus raphanistrum plant in a cereal crop. Claim 16: The composition of claim 15, wherein the photosystem inhibitor II is selected from the group consisting of ametrine, atrazine, cyanazine, hexazinone, metribuzine and simazine. Claim 17: The composition of claim 16, wherein the photosystem II inhibitor is metribuzine.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461972457P | 2014-03-31 | 2014-03-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR099865A1 true AR099865A1 (en) | 2016-08-24 |
Family
ID=54241124
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP150100913A AR099865A1 (en) | 2014-03-31 | 2015-03-27 | METHODS FOR SELECTLY CONTROLLING PLANTS USING COMPOSITIONS CONTAINING PHOTOSYSTEM II INHIBITORS AND OXIDASE PROTOPORPHYRINOGEN INHIBITORS |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP3125693A4 (en) |
| AR (1) | AR099865A1 (en) |
| AU (1) | AU2015241224B2 (en) |
| EA (1) | EA030031B1 (en) |
| WO (1) | WO2015153281A1 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA125828C2 (en) | 2017-06-13 | 2022-06-15 | Монсанто Текнолоджі Ллс | MICROENCAPSULATED HERBICIDES |
| BR102017019120B1 (en) | 2017-09-06 | 2023-01-31 | UPL Corporation Limited | MIXTURE COMPRISING A FOLCYSTEIN-BASED BIO-STIMULANT AND AN INSECTICIDE OBTAINING POTENTIALIZING ACTION FROM THE RESULTS OF QUALITATIVE, QUANTITATIVE AND TEMPORAL ORDER OBSERVED IN AN AGRICULTURAL CULTURE OF A PLANT OF INTEREST |
| BR102018075132A2 (en) * | 2018-12-04 | 2020-06-16 | UPL Corporation Limited | WIDE SPECTRUM SYNERGISTIC HERBICIDE COMPOSITION FOR THE CONTROL OF WEEDS IN AGRICULTURAL CROPS, USE OF THESE COMPOSITION FOR PREPARATION OF PRODUCT, PRODUCT AND APPLICATION METHOD |
| CN111616151A (en) * | 2020-07-15 | 2020-09-04 | 青海省农林科学院 | Chemical herbicide composition and application thereof |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2734453B1 (en) * | 1995-05-24 | 1997-07-25 | Francais Prod Ind Cfpi | TREATMENT AND IMPROVED HERBICIDE COMPOSITION BASED ON AMINOTRIAZOLE AND METHOD FOR IMPLEMENTING THE COMPOSITION |
| DE19836700A1 (en) * | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Use of a synergistic herbicide combination including a glufosinate- or glyphosate-type, imidazolinone or protoporphyrinogen oxidase inhibitory azole herbicide to control weeds in cereals |
| AR021121A1 (en) * | 1998-11-10 | 2002-06-12 | Syngenta Participations Ag | HERBICIDE COMPOSITION |
| ES2592264T3 (en) * | 2004-02-11 | 2016-11-29 | Fmc Corporation | Bryum Argenteum control method |
| US7939721B2 (en) * | 2006-10-25 | 2011-05-10 | Monsanto Technology Llc | Cropping systems for managing weeds |
| ES2588779T3 (en) * | 2007-08-27 | 2016-11-04 | Dow Agrosciences Llc | Synergistic herbicidal composition containing certain pyridine carboxylic acids and certain herbicides for cereal and rice |
| US20110015068A1 (en) * | 2008-03-17 | 2011-01-20 | Basf Se | Herbicidal Compositions Comprising Pyroxasulfone V |
| CN102342279B (en) * | 2011-06-03 | 2014-06-18 | 陕西韦尔奇作物保护有限公司 | Weeding composition containing carfentrazone-ethyl and triazine |
| CN102428941B (en) * | 2011-11-09 | 2013-08-21 | 山东胜邦绿野化学有限公司 | Compound weedicide and preparation method thereof |
| US8791048B2 (en) * | 2012-07-24 | 2014-07-29 | Dow Agrosciences Llc | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and clomazone |
| CN105409983B (en) * | 2015-11-25 | 2018-02-02 | 山东滨农科技有限公司 | A kind of corn field herbicide composition |
-
2015
- 2015-03-26 EP EP15773960.8A patent/EP3125693A4/en not_active Withdrawn
- 2015-03-26 EA EA201691926A patent/EA030031B1/en unknown
- 2015-03-26 WO PCT/US2015/022740 patent/WO2015153281A1/en not_active Ceased
- 2015-03-26 AU AU2015241224A patent/AU2015241224B2/en active Active
- 2015-03-27 AR ARP150100913A patent/AR099865A1/en active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| EA201691926A1 (en) | 2017-01-30 |
| AU2015241224A1 (en) | 2016-10-13 |
| EP3125693A1 (en) | 2017-02-08 |
| AU2015241224B2 (en) | 2018-01-25 |
| EP3125693A4 (en) | 2017-08-16 |
| EA030031B1 (en) | 2018-06-29 |
| WO2015153281A1 (en) | 2015-10-08 |
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