MA30396B1 - Melanges herbicides - Google Patents
Melanges herbicidesInfo
- Publication number
- MA30396B1 MA30396B1 MA31350A MA31350A MA30396B1 MA 30396 B1 MA30396 B1 MA 30396B1 MA 31350 A MA31350 A MA 31350A MA 31350 A MA31350 A MA 31350A MA 30396 B1 MA30396 B1 MA 30396B1
- Authority
- MA
- Morocco
- Prior art keywords
- inhibitors
- herbicide
- auxine
- flamprop
- photosystem
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract 8
- 230000002363 herbicidal effect Effects 0.000 title abstract 7
- 239000000203 mixture Substances 0.000 title abstract 4
- 239000003112 inhibitor Substances 0.000 abstract 8
- 239000000729 antidote Substances 0.000 abstract 2
- 239000003525 auxine Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 abstract 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 abstract 1
- AHXUVTKVCMOKIX-UHFFFAOYSA-N 1-bromo-4-(chloromethylsulfonyl)benzene Chemical compound ClCS(=O)(=O)C1=CC=C(Br)C=C1 AHXUVTKVCMOKIX-UHFFFAOYSA-N 0.000 abstract 1
- MCNOFYBITGAAGM-UHFFFAOYSA-N 2,2-dichloro-1-[5-(furan-2-yl)-2,2-dimethyl-1,3-oxazolidin-3-yl]ethanone Chemical compound C1N(C(=O)C(Cl)Cl)C(C)(C)OC1C1=CC=CO1 MCNOFYBITGAAGM-UHFFFAOYSA-N 0.000 abstract 1
- OHXLAOJLJWLEIP-UHFFFAOYSA-N 2-(dichloromethyl)-2-methyl-1,3-dioxolane Chemical compound ClC(Cl)C1(C)OCCO1 OHXLAOJLJWLEIP-UHFFFAOYSA-N 0.000 abstract 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 abstract 1
- 108010020183 3-phosphoshikimate 1-carboxyvinyltransferase Proteins 0.000 abstract 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 abstract 1
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 abstract 1
- 239000005499 Clomazone Substances 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
- 239000005644 Dazomet Substances 0.000 abstract 1
- LBGPXIPGGRQBJW-UHFFFAOYSA-N Difenzoquat Chemical compound C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 LBGPXIPGGRQBJW-UHFFFAOYSA-N 0.000 abstract 1
- ICWUMLXQKFTJMH-UHFFFAOYSA-N Etobenzanid Chemical compound C1=CC(OCOCC)=CC=C1C(=O)NC1=CC=CC(Cl)=C1Cl ICWUMLXQKFTJMH-UHFFFAOYSA-N 0.000 abstract 1
- GMBRUAIJEFRHFQ-UHFFFAOYSA-N Fenchlorazole-ethyl Chemical compound N1=C(C(=O)OCC)N=C(C(Cl)(Cl)Cl)N1C1=CC=C(Cl)C=C1Cl GMBRUAIJEFRHFQ-UHFFFAOYSA-N 0.000 abstract 1
- NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-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
- UKSLKNUCVPZQCQ-UHFFFAOYSA-N Fluxofenim Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)=NOCC1OCCO1 UKSLKNUCVPZQCQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005571 Isoxaflutole Substances 0.000 abstract 1
- -1 METHYLDYMRONE Chemical compound 0.000 abstract 1
- 239000005578 Mesotrione Substances 0.000 abstract 1
- BWPYBAJTDILQPY-UHFFFAOYSA-N Methoxyphenone Chemical compound C1=C(C)C(OC)=CC=C1C(=O)C1=CC=CC(C)=C1 BWPYBAJTDILQPY-UHFFFAOYSA-N 0.000 abstract 1
- GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 abstract 1
- 239000005642 Oleic acid Substances 0.000 abstract 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005643 Pelargonic acid Substances 0.000 abstract 1
- 108010081996 Photosystem I Protein Complex Proteins 0.000 abstract 1
- 108010060806 Photosystem II Protein Complex Proteins 0.000 abstract 1
- XIPUIGPNIDKXJU-UHFFFAOYSA-N [CH]1CC1 Chemical group [CH]1CC1 XIPUIGPNIDKXJU-UHFFFAOYSA-N 0.000 abstract 1
- 239000000370 acceptor Substances 0.000 abstract 1
- 229940075522 antidotes Drugs 0.000 abstract 1
- VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 abstract 1
- 208000014347 autosomal dominant hyaline body myopathy Diseases 0.000 abstract 1
- OTSAMNSACVKIOJ-UHFFFAOYSA-N azane;carbamoyl(ethoxy)phosphinic acid Chemical compound [NH4+].CCOP([O-])(=O)C(N)=O OTSAMNSACVKIOJ-UHFFFAOYSA-N 0.000 abstract 1
- MKQSWTQPLLCSOB-UHFFFAOYSA-N benzyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate Chemical compound N1=C(Cl)SC(C(=O)OCC=2C=CC=CC=2)=C1C(F)(F)F MKQSWTQPLLCSOB-UHFFFAOYSA-N 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- WZDDLAZXUYIVMU-UHFFFAOYSA-N bromobutide Chemical compound CC(C)(C)C(Br)C(=O)NC(C)(C)C1=CC=CC=C1 WZDDLAZXUYIVMU-UHFFFAOYSA-N 0.000 abstract 1
- KIEDNEWSYUYDSN-UHFFFAOYSA-N clomazone Chemical compound O=C1C(C)(C)CON1CC1=CC=CC=C1Cl KIEDNEWSYUYDSN-UHFFFAOYSA-N 0.000 abstract 1
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 abstract 1
- OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical compound CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 abstract 1
- SDIXRDNYIMOKSG-UHFFFAOYSA-L disodium methyl arsenate Chemical compound [Na+].[Na+].C[As]([O-])([O-])=O SDIXRDNYIMOKSG-UHFFFAOYSA-L 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- COYBRKAVBMYYSF-UHFFFAOYSA-N heptan-2-yl [(5-chloroquinolin-8-yl)oxy]acetate Chemical compound C1=CN=C2C(OCC(=O)OC(C)CCCCC)=CC=C(Cl)C2=C1 COYBRKAVBMYYSF-UHFFFAOYSA-N 0.000 abstract 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 abstract 1
- MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical compound C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-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
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 abstract 1
- RBNIGDFIUWJJEV-LLVKDONJSA-N methyl (2r)-2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical compound C=1C=C(F)C(Cl)=CC=1N([C@H](C)C(=O)OC)C(=O)C1=CC=CC=C1 RBNIGDFIUWJJEV-LLVKDONJSA-N 0.000 abstract 1
- JITOKQVGRJSHHA-UHFFFAOYSA-M monosodium methyl arsenate Chemical compound [Na+].C[As](O)([O-])=O JITOKQVGRJSHHA-UHFFFAOYSA-M 0.000 abstract 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 1
- IKVXBIIHQGXQRQ-CYBMUJFWSA-N propan-2-yl (2r)-2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical compound C=1C=C(F)C(Cl)=CC=1N([C@H](C)C(=O)OC(C)C)C(=O)C1=CC=CC=C1 IKVXBIIHQGXQRQ-CYBMUJFWSA-N 0.000 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
- 150000003230 pyrimidines Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 150000004669 very long chain fatty acids Chemical class 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
- A01N33/18—Nitro compounds
- A01N33/20—Nitro compounds containing oxygen or sulfur attached to the carbon skeleton containing the nitro group
- A01N33/22—Nitro compounds containing oxygen or sulfur attached to the carbon skeleton containing the nitro group having at least one oxygen or sulfur atom and at least one nitro group directly attached to the same aromatic ring system
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
- A01N39/04—Aryloxy-acetic acids; Derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
LA PRÉSENTE INVENTION CONCERNE UN MÉLANGE HERBICIDE COMPRENANT (A) AU MOINS UN COMPOSÉ HERBICIDE CHOISI PARMI LES PYRIMIDINES DE FORMULE (I), Y COMPRIS TOUS LES ISOMÈRES GÉOMÉTRIQUES ET LES STÉRÉOISOMÈRES, LES N-OXYDES ET LES SELS DE CELLES-CI. DANS LA FORMULE (1) : R1 REPRÉSENTE CYCLOPROPYLE, 4-BR-PHÉNYLE OU 4-CL-PHÉNYLE; X REPRÉSENTE CL OU BR; R2 REPRÉSENTE H, ALKYLE C1-C14, ALKOXYALKYLE C2-C14, ALKOXYALKOXYALKYLE C3-C14, HYDROXYALKYLE C2-C14 OU BENZYLE; ET (B) AU MOINS UN COMPOSÉ HERBICIDE OU ANTIDOTE D'HERBICIDE SUPPLÉMENTAIRE CHOISI DANS LE GROUPE FORMÉ PAR (B1) DES INHIBITEURS DE L'ACCASE, (B2) DES INHIBITEURS DE L'AHAS, (B3) DES INHIBITEURS DU PHOTOSYSTÈME II, (B4) DES ACCEPTEURS D'ÉLECTRONS DU PHOTOSYSTÈME I, (B5) DES INHIBITEURS DE LA PPO, (B6) DES INHIBITEURS DE LA EPSP SYNTHASE, (B7) DES INHIBITEURS DE LA GS, (B8) DES INHIBITEURS DE VLCFA, (B9) DES ANALOGUES D'AUXINE, (B10) DES INHIBITEURS DE TRANSPORT D'AUXINE, (B11) D'AUTRES HERBICIDES CHOISIS DANS LE GROUPE FORMÉ PAR LE FLAMPROP-M-MÉTHYLE, LE FLAMPROP-M-ISOPROPYLE, LE DIFENZOQUAT, LE DSMA, LE MSMA, LE BROMOBUTIDE, LE FLURÉNOL, LE CINMÉTHYLINE, LA CUMYLURONE, LE DAZOMET, LA DYMRONE, LA MÉTHYLDYMRONE, L'ÉTOBENZANIDE, LE FOSAMINE-AMMONIUM, L'ISOXAFLUTOLE, L'ASULAME, LA CLOMAZONE, LA MÉSOTRIONE, LE MÉTAME, L'OXAZICLOMÉFONE, L'ACIDE OLÉIQUE, L'ACIDE PÉLARGONIQUE ET LE PYRIBUTICARBE, (B12) DES ANTIDOTES D'HERBICIDE CHOISIS DANS LE GROUPE FORMÉ PAR LE BÉNOXACOR, LE 1-BROMO-4-[(CHLOROMÉTHYL)SULFONYL]BENZÈNE, LE CLOQUINTOCET-MEXYL, LE CYOMÉTRINILE, LE DICHLORMIDE, LE 2-(DICHLOROMÉTHYL)-2-MÉTHYL-1,3-DIOXOLANE, LE FENCHLORAZOLE-ÉTHYLE, LE FENCLORIM, LE FLURAZOLE, LE FLUXOFÉNIM, LE FURILAZOLE, L'ISOXADIFÈNE-ÉTHYLE, LE MEFÈNPYR-DIÉTHYLE, LA MÉTHOXYPHÉNONE, L'ANHYDRIDE NAPHTALIQUE ET L'OXABÉTRINILE ET DES SELS DE CEUX-CI. CETTE INVENTION CONCERNE ÉGALEMENT UN PROCÉDÉ PERMETTANT DE MAÎTRISER LA CROISSANCE D'UNE VÉGÉTATION NON DÉSIRABLE. CE PROCÉDÉ CONSISTE À METTRE EN CONTACT LADITE VÉGÉTATION OU SON ENVIRONNEMENT AVEC UNE QUANTITÉ EFFICACE POUR OBTENIR UN EFFET HERBICIDE D'UN MÉLANGE SELON CETTE INVENTION (C'EST-À-DIRE D'UNE COMPOSITION TELLE QUE SUSMENTIONNÉE).
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79065906P | 2006-04-10 | 2006-04-10 | |
| US85213906P | 2006-10-17 | 2006-10-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA30396B1 true MA30396B1 (fr) | 2009-05-04 |
Family
ID=38450698
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA31350A MA30396B1 (fr) | 2006-04-10 | 2008-11-03 | Melanges herbicides |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US20100285959A1 (fr) |
| EP (1) | EP2003972A2 (fr) |
| JP (1) | JP2009533448A (fr) |
| KR (1) | KR20090024120A (fr) |
| AR (1) | AR060415A1 (fr) |
| AU (1) | AU2007238732A1 (fr) |
| BR (1) | BRPI0709505A2 (fr) |
| CA (1) | CA2646143A1 (fr) |
| EA (1) | EA200870419A1 (fr) |
| EC (1) | ECSP088802A (fr) |
| IL (1) | IL193767A0 (fr) |
| MA (1) | MA30396B1 (fr) |
| MX (1) | MX2008012995A (fr) |
| TN (1) | TNSN08519A1 (fr) |
| WO (1) | WO2007120706A2 (fr) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL2514314T3 (pl) * | 2007-08-27 | 2017-08-31 | Dow Agrosciences Llc | Synergistyczna kompozycja chwastobójcza zawierająca pewne kwasy pirydynokarboksylowe oraz pewne herbicydy stosowane w uprawie zbóż i ryżu |
| PL2193120T3 (pl) | 2007-10-02 | 2017-01-31 | Dow Agrosciences Llc | Kwasy 2'podstowione-6-amino-5-alkilo-, alkenylo- lub alkinylo-4-pirymidynokarboksylowe i kwasy 6-podstawione-4-amino-3-alkilo-, alkenylo- lub alkinylopikolinowe oraz ich zastosowanie jako herbicydy |
| EP2052613A1 (fr) * | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Combinaison d'herbicide |
| BRPI0912469B1 (pt) * | 2008-08-12 | 2018-07-03 | E.I. Du Pont De Nemours And Company | Método para o controle de vegetação indesejada |
| EP2191720A1 (fr) * | 2008-11-29 | 2010-06-02 | Bayer CropScience AG | Combinaison d'herbicide-phytoprotecteur |
| EP2191716A1 (fr) | 2008-11-29 | 2010-06-02 | Bayer CropScience AG | Combinaison d'herbicide-phytoprotecteur |
| AU2010210374A1 (en) * | 2009-02-06 | 2011-09-22 | University Of Tennessee Research Foundation | Novel herbicide resistance gene |
| US9408387B2 (en) * | 2009-10-29 | 2016-08-09 | Dow Agrosciences Llc | Safening 6-amino-2-(substituted phenyl)-5-substituted-4-pyrimidinecarboxylate herbicide injury on cereal crops |
| US20110287933A1 (en) | 2010-05-21 | 2011-11-24 | Bayer Cropscience Ag | Herbicidal composition for tolerant or resistant oilseed rape crops |
| CA2799692A1 (fr) | 2010-05-21 | 2011-11-24 | Bayer Intellectual Property Gmbh | Agents herbicides pour cultures de cereales tolerantes ou resistantes |
| EP2571366A1 (fr) | 2010-05-21 | 2013-03-27 | Bayer Intellectual Property GmbH | Agents herbicides pour cultures de maïs tolérantes ou résistantes |
| EP2571364A1 (fr) | 2010-05-21 | 2013-03-27 | Bayer Intellectual Property GmbH | Agents herbicides pour cultures de riz tolérantes ou résistantes |
| GB2484982A (en) * | 2010-10-29 | 2012-05-02 | Syngenta Ltd | Safeners for a pyrimidine derivative herbicides |
| TWI596088B (zh) * | 2011-01-25 | 2017-08-21 | 陶氏農業科學公司 | ４－胺基－６－（經取代的苯基）吡啶甲酸酯及６－胺基－２－（經取代的苯基）－４－嘧啶羧酸酯之芳烷酯以及其等作為除草劑之用途 |
| WO2012135441A1 (fr) * | 2011-03-30 | 2012-10-04 | Dow Agrosciences Llc | Le pénoxsulam comme herbicide pour la luzerne |
| BR112014001882B1 (pt) | 2011-07-27 | 2019-05-07 | Bayer Intellectual Property Gmbh | Composições herbicidas, uso de ácidos picolínicos e ácidos pirimidina-4-carboxílicos substituídos, e método para controlar plantas indesejadas |
| AR089283A1 (es) | 2011-12-27 | 2014-08-13 | Ishihara Sangyo Kaisha | Composicion herbicida |
| CN104754946B (zh) | 2012-09-04 | 2019-08-16 | 美国陶氏益农公司 | 施用氯丙嘧啶酸和二氯吡啶酸所引起的协同杂草防治 |
| WO2014052805A1 (fr) | 2012-09-28 | 2014-04-03 | Dow Agrosciences Llc | Lutte synergique contre les mauvaises herbes par des applications d'aminocyclopyrachlore et d'aminopyralide |
| AU2013323276B2 (en) * | 2012-09-28 | 2016-10-13 | Corteva Agriscience Llc | Synergistic weed control from applications of aminocyclopyrachlor and fluroxypyr |
| WO2014052819A1 (fr) | 2012-09-28 | 2014-04-03 | Dow Agrosciences Llc | Désherbage synergique par applications d'aminocyclopyrachlore et de triclopyr |
| US20140128262A1 (en) * | 2012-11-05 | 2014-05-08 | Valent U.S.A. Corporation | Compositions and Methods for Residual Weed Control With PPO Inhibitors and Gibberellic Acid |
| US9426991B2 (en) * | 2012-12-12 | 2016-08-30 | Dow Agrosciences Llc | Synergistic weed control from applications of aminocyclopyrachlor and picloram |
| US9149037B2 (en) | 2012-12-12 | 2015-10-06 | Dow Agrosciences Llc | Synergistic weed control from applications of aminocyclopyrachlor and 2,4 dichlorophenoxyacetic acid (2,4-D) |
| US10412964B2 (en) | 2012-12-14 | 2019-09-17 | Dow Agrosciences Llc | Synergistic weed control from applications of aminopyralid and clopyralid |
| HUE042793T2 (hu) | 2012-12-14 | 2019-07-29 | Dow Agrosciences Llc | Szinergetikus gyomirtás aminopiralid és klopiralid alkalmazásával |
| EP2934112B1 (fr) | 2012-12-21 | 2019-05-08 | Dow Agrosciences LLC | Herbicide contenant de l'aminopyralide, du triclopyr et un agent de surface organosilicié |
| EA026809B1 (ru) | 2012-12-21 | 2017-05-31 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Термостабильные водные композиции клоквинтосет-мексила |
| CN105120661B (zh) | 2013-02-25 | 2018-08-07 | 美国陶氏益农公司 | 菠萝中的杂草防治方法 |
| AR101863A1 (es) | 2014-09-15 | 2017-01-18 | Dow Agrosciences Llc | Control sinérgico de malezas a partir de aplicaciones de herbicidas de ácido piridín carboxílico e inhibidores de fotosistema ii |
| AR101858A1 (es) * | 2014-09-15 | 2017-01-18 | Dow Agrosciences Llc | Composiciones herbicidas protegidas que comprenden un herbicida de ácido piridincarboxílico |
| TWI685302B (zh) | 2014-09-15 | 2020-02-21 | 美商陶氏農業科學公司 | 包含吡啶羧酸除草劑之安全的除草組成物 |
| TWI689251B (zh) * | 2014-09-15 | 2020-04-01 | 美商陶氏農業科學公司 | 源自於施用吡啶羧酸除草劑與合成生長素除草劑及/或生長素轉運抑制劑的協同性雜草控制 |
| TWI689252B (zh) * | 2014-09-15 | 2020-04-01 | 美商陶氏農業科學公司 | 源自於施用吡啶羧酸除草劑與乙醯乳酸合成酶（ａｌｓ）抑制劑的協同性雜草控制 |
| EP3675635A4 (fr) * | 2017-09-01 | 2021-05-19 | Dow Agrosciences LLC | Compositions herbicides contenant des acides pyridine carboxyliques ou des dérivés de ceux-ci, avec du glyphosate ou du glufosinate, ou des dérivés de ceux-ci |
| BR102017019120B1 (pt) | 2017-09-06 | 2023-01-31 | UPL Corporation Limited | Mistura compreendendo um bioestimulante à base de folcisteína e um inseticida obtendo ação potencializadora dos resultados de ordens qualitativa, quantitativa e temporal observados em uma cultura agrícola de uma planta de interesse |
| WO2020172305A1 (fr) | 2019-02-19 | 2020-08-27 | Gowan Company, L.L.C. | Compositions liquides stables et leurs procédés d'utilisation |
| WO2020196285A1 (fr) * | 2019-03-27 | 2020-10-01 | 住友化学株式会社 | Procédé de lutte contre les mauvaises herbes |
| EP4140981B1 (fr) * | 2020-04-21 | 2025-02-12 | Kumiai Chemical Industry Co., Ltd. | Utilisation d'une composition d'inhibiteur de production de méthane et procédé d'inhibition de la production de méthane |
| CA3249238A1 (fr) * | 2022-01-31 | 2023-08-03 | The Board Of Trustees Of The University Of Arkansas | Traitement de semences pour la phytoprotection du blé vis-à-vis d’herbicides à base de chloroacétamide |
| PL248303B1 (pl) * | 2022-12-29 | 2025-11-24 | Univ Slaski | Kompozycja poprawiająca penetrację herbicydu przez powierzchnie części nadziemnych organów roślinnych |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH595061A5 (fr) * | 1974-05-10 | 1978-01-31 | Ciba Geigy Ag | |
| EP0136976A3 (fr) * | 1983-08-23 | 1985-05-15 | Ciba-Geigy Ag | Application de phénylpyrimidines comme régulateurs pour plantes |
| CZ301614B6 (cs) * | 2000-05-22 | 2010-05-05 | Bayer Cropscience Ag | Herbicidní prostredek, zpusob jeho výroby a jeho použití pro hubení nežádoucích rostlin |
| TWI355894B (en) * | 2003-12-19 | 2012-01-11 | Du Pont | Herbicidal pyrimidines |
| WO2006124657A1 (fr) * | 2005-05-16 | 2006-11-23 | E. I. Du Pont De Nemours And Company | Procede pour preparer des pyrimidines substituees |
-
2007
- 2007-04-10 AR ARP070101511A patent/AR060415A1/es not_active Application Discontinuation
- 2007-04-10 KR KR1020087027364A patent/KR20090024120A/ko not_active Ceased
- 2007-04-10 CA CA002646143A patent/CA2646143A1/fr not_active Abandoned
- 2007-04-10 EA EA200870419A patent/EA200870419A1/ru unknown
- 2007-04-10 JP JP2009505457A patent/JP2009533448A/ja not_active Abandoned
- 2007-04-10 AU AU2007238732A patent/AU2007238732A1/en not_active Abandoned
- 2007-04-10 EP EP07755262A patent/EP2003972A2/fr not_active Withdrawn
- 2007-04-10 WO PCT/US2007/008930 patent/WO2007120706A2/fr not_active Ceased
- 2007-04-10 US US12/296,474 patent/US20100285959A1/en not_active Abandoned
- 2007-04-10 BR BRPI0709505-8A patent/BRPI0709505A2/pt not_active Application Discontinuation
- 2007-04-10 MX MX2008012995A patent/MX2008012995A/es not_active Application Discontinuation
-
2008
- 2008-08-28 IL IL193767A patent/IL193767A0/en unknown
- 2008-10-08 EC EC2008008802A patent/ECSP088802A/es unknown
- 2008-11-03 MA MA31350A patent/MA30396B1/fr unknown
- 2008-12-16 TN TNP2008000519A patent/TNSN08519A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EA200870419A1 (ru) | 2009-02-27 |
| EP2003972A2 (fr) | 2008-12-24 |
| CA2646143A1 (fr) | 2007-10-25 |
| TNSN08519A1 (en) | 2010-04-14 |
| AU2007238732A1 (en) | 2007-10-25 |
| MX2008012995A (es) | 2008-10-17 |
| WO2007120706A2 (fr) | 2007-10-25 |
| ECSP088802A (es) | 2008-11-27 |
| AR060415A1 (es) | 2008-06-18 |
| BRPI0709505A2 (pt) | 2011-07-19 |
| IL193767A0 (en) | 2009-05-04 |
| WO2007120706A3 (fr) | 2008-05-29 |
| KR20090024120A (ko) | 2009-03-06 |
| JP2009533448A (ja) | 2009-09-17 |
| US20100285959A1 (en) | 2010-11-11 |
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