EP1298996A1 - Herbicides selectifs a base d'heteroaryloxy-acetamides - Google Patents
Herbicides selectifs a base d'heteroaryloxy-acetamidesInfo
- Publication number
- EP1298996A1 EP1298996A1 EP01943335A EP01943335A EP1298996A1 EP 1298996 A1 EP1298996 A1 EP 1298996A1 EP 01943335 A EP01943335 A EP 01943335A EP 01943335 A EP01943335 A EP 01943335A EP 1298996 A1 EP1298996 A1 EP 1298996A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- methyl
- ethyl
- chloro
- phenyl
- dihydro
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
Definitions
- the invention relates to new selective herbicidal, synergistic active ingredient combinations which consist of known heteroaryloxyacetamides on the one hand and known herbicidally active compounds and / or compounds which improve the tolerance of crop plants on the other hand and which are used with particularly good success for selective weed control in various crop plants can.
- Heteroaryloxyacetamides as strong herbicides which are particularly effective against monocotyledon weeds, are the subject of a number of patent applications (cf. EP-A 5501, EP-A 18497, EP-A 29171, EP-A 94514, EP-A 100044, EP-A 100045, EP -A 161602, EP-A 195237, EP-A 348734, EP-A 348737, DE-A 4317323).
- EP-A 5501, EP-A 18497, EP-A 29171, EP-A 94514, EP-A 100044, EP-A 100045, EP -A 161602, EP-A 195237, EP-A 348734, EP-A 348737, DE-A 4317323 are the subject of a number of patent applications.
- active substance combinations are heteroaryloxyacetamides and other herbicidally active compounds to achieve a synergistic effect (cf. WO-A 94/02014, WO-A-96/07323, WO-A-96/11575, WO-A-96/17519 , WO-A-
- the invention relates to selective herbicidal compositions, characterized by an effective content of an active ingredient combination consisting of
- Ar represents phenyl which is optionally substituted by halogen, C 4 -C 4 -alkyl or C 4 -C 4 -haloalkyl,
- Het is thiadiazolyl which is substituted by halogen or by C1-C4-alkyl or phenyl which is optionally substituted by halogen, and
- R represents alkyl, alkenyl or alkynyl each having up to 4 carbon atoms
- Ethyl 4,5-dihydro-5,5-diphenyl-3-isoxazole carboxylate isoxadifen-ethyl
- diethyl l- (2,4-dichlorophenyl) -4,5-dihydro-5-methyl-1H-pyrazole -3,5-dicarboxy-lat mefenpyr-diethyl
- 2-dichloromethyl-2-methyl-1,3-dioxolane MG-191, 1,8-naphthalic acid anhydride, ⁇ - (1,3-dioxolane-2 -yl-methoximino) -phenylaceto-nitrile (oxabetrinil), 2,2-dichloro-N- (1,3-dioxolan-2-yl-methyl) -N- (2-propenyl) -acetamide (PPG-1292), 3-dichloroacetyl-2,2-dimethyl-oxazolidine (R-2
- Ar preferably represents phenyl optionally substituted by fluorine, chlorine, bromine, methyl, ethyl or trifluoromethyl.
- Het preferably stands for 1,2,4-thiadiazolyl or 1,3,4-thiadiazolyl, which by fluorine, chlorine, bromine or by optionally by fluorine and / or Chlorine substituted methyl, ethyl, n- or i-propyl or phenyl is substituted.
- R preferably represents methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, 2-propenyl, l-methyl-2-propenyl, 2-butenyl, 2-propynyl, 1- Methyl 2-propynyl, 2-butynyl.
- Ar particularly preferably represents phenyl optionally substituted by fluorine, chlorine, bromine, methyl or trifluoromethyl.
- Het is particularly preferably 1,2,4-thiadiazolyl or 1,3,4-thiadiazolyl, which is substituted by fluorine, chlorine, bromine or by methyl, ethyl or phenyl which are optionally substituted by fluorine and / or chlorine.
- R particularly preferably represents methyl, ethyl, n- or i-propyl, n-, i-, s- or t-
- Ar very particularly preferably represents phenyl optionally substituted by fluorine or chlorine.
- Het very particularly preferably represents 1,3,4-thiadiazolyl which is substituted by chlorine, bromine or by fluorine- and / or chlorine-substituted methyl.
- R very particularly preferably represents methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl.
- Examples of the compounds of the formula (I) to be used as mixture partners according to the invention are: Ni-propyl-N-phenyl- ⁇ - (5-trifluoromethyl-l, 3,4-thiadiazol-2-yl-oxy) -acetamide, Ni-propyl-N- (2-chlorophenyl) - ⁇ - (5th -trifluora ⁇ ethyl-l, 3,4-thiadiazol-2-yl-oxy) -acetamide, Ni-propyl-N- (3-chlorophenyl) - ⁇ - (5-trifluoromethyl-l, 3,4-thiadiazol-2 -yl-oxy) -acetamide, Ni-propyl-N- (4-chlorophenyl) - ⁇ - (5-trifluoromethyl-l, 3,4-thiadiazol-2-yl-oxy) - acetamide, Ni Propyl-N- (2-fluoro-phenyl) - ⁇ - (5-trifluoromethyl-1, 3,
- the active substances of group 2 can be assigned to their chemical structure according to the following active substance classes:
- Amides e.g. beflubutamide
- aryl heterocycles e.g. azafenidin, benzfendizone
- Butroxydim, Clefoxydim, Cycloxydim), dinitroanilines e.g. Benfluralin, Oryzalin
- imidazoxones e.g. Imazamoxolinone
- Isoxachlortole e.g. Isoxachlortole
- pyridines e.g. Thiazopyr
- pyrimidinyl (thio) benzoates e.g. Pyribenz-oxim, Pyriftalid, Pyriminobac-methyl, Pyrithiobac-sodium
- sulfonylureas e.g.
- Azimsulfuron Flupyrsulfuron-methyl-sodium, Foramsulfuron-methyl- Iodosulfuron sodium, mesosul Someon, trifloxysulfuron, triflusulfuron-methyl), tetrazolinones (e.g.
- Fentrazamides Fentrazamides
- triazoles e.g. amitroles
- triazolinones e.g. flucarbazone-sodium, Procarbazone-sodium
- triazolopyrimidines e.g. cloransulam-methyl, diclosulam, florasulam
- triketones e.g. mesotrione
- mixture components from the active ingredients of group 2 are:
- Azimsulfuron Beflubuta id, Butafenacil-allyl, Cinidon-ethyl, Cloransulam-methyl, Clefoxydim, Diclosulam, Fenoxaprop-P-ethyl, Florasulam, Flupyrsul possiblyon-methyl-sodium, Foramsulmron, Imazamox, Iodosulfuron-methyl-sodium, Oxox, Isox , Procarbazone-sodium, pyriftalid, pyrithiobac-sodium, quinclorac, trifloxysulfuron.
- beflubutamide is of particular interest as a mixture component.
- butafenacil-allyl is of particular interest as a mixture component.
- cinidon-ethyl is of particular interest as a mixture component.
- Clefoxydim is also of particular interest as a mixture component.
- cloransulam-methyl is also of particular interest as a mixture component.
- flupyrsulfuron-methyl-sodium is of particular interest as a mixture component.
- imazamox is also of particular interest as a mixture component.
- iodosulfuron-methyl-sodium is of particular interest as a mixture component.
- mesosullayson is also of particular interest as a mixture component.
- oxaziclomefone is also of particular interest as a mixture component.
- Procarbazone-sodium from this group is of particular interest as a mixture component.
- agents according to the invention preferably contain one or two active substances from group 1, one to three active substances from group 2 and optionally an active substance from group 3.
- the agents according to the invention contain an active ingredient of group 1, one or two active ingredients of group 2 and optionally an active ingredient of group 3.
- Active ingredients of group 2 with a largely good crop tolerance have a particularly high herbicidal activity and can be used in various crops, in particular in barley, potatoes, corn, rice, soybeans and wheat, for the selective control of monocotyledonous and dicotyledonous weeds and that they can also be used for Control of monocot and dicot weeds in the semi and non-selective range can be used.
- the herbicidal activity of the active compound combinations according to the invention consisting of compounds from groups 1 and 2 listed above is considerably higher than the sum of the effects of the individual active compounds.
- the new active ingredient combinations are well tolerated in many crops, and the new active ingredient combinations also combat weeds that are otherwise difficult to control.
- the new active ingredient combinations thus represent a valuable addition to the herbicides.
- the synergistic effect of the active compound combinations according to the invention is particularly pronounced at certain concentration ratios.
- the weight ratios of the active ingredients in the active ingredient combinations can be varied within relatively large ranges.
- 1 part by weight of active Substance of the formula (I) 0.01 to 1000 parts by weight, preferably 0.02 to 500 parts by weight and particularly preferably 0.05 to 100 parts by weight of active ingredient or active ingredients of group 2.
- the group 3 compounds listed above are particularly suitable, the harmful effect of active compounds of the formula ( I) and their salts, if appropriate also in combination with one or more of the active ingredients of group 2 mentioned above, to be completely removed from the crop plants without impairing the herbicidal activity against the weeds.
- the advantageous effect of the crop plant compatibility of the active compound combinations according to the invention is also particularly pronounced at certain concentration ratios.
- the weight ratios of the active ingredients in the active ingredient combinations can be varied within relatively large ranges. In general, 1 part by weight of active compound of the formula (I) or mixtures thereof are present
- Active substances of group 2 0.001 to 1000 parts by weight, preferably 0.01 to 100 parts by weight and particularly preferably 0.1 to 10 parts by weight of active substance or active substances of group 3.
- Plants are understood to mean all plants and plant populations, such as desired and undesired wild plants or crop plants (including naturally occurring crop plants).
- Cultivated plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including the plant cultivars which can or cannot be protected by plant breeders' rights.
- Plant parts are to be understood to mean all above-ground and underground plant parts and organs of plants, such as shoots, leaves, flowers and roots, examples being leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds and
- Roots, tubers and rhiozomes are listed.
- the plant parts also include vegetative and generative propagation material, for example cuttings, tubers, rhizomes, offshoots and seeds.
- the treatment according to the invention of the plants and parts of plants with the active compounds takes place directly or by acting on their surroundings, living space or storage space according to the customary treatment methods, for example by dipping, spraying, evaporating, atomizing, scattering, spreading and, in the case of propagation material, in particular seeds, by - or multi-layer wrapping.
- the plants obtained by biotechnological and genetic engineering methods or by a combination of these methods those plants are emphasized which tolerate so-called 4-HPPD, EPSP and / or PPO materials, such as, for example, acuron plants.
- the active compounds according to the invention can e.g. can be used in the following plants:
- the active ingredient combinations to be used according to the invention can be used both in conventional cultivation processes (row crops with a suitable row width) in plantation crops (for example wine, fruit, citrus) and in industrial and track systems, on paths and squares, but also for stubble treatment and with the minimum tillage process become. They are also suitable as burners (herb killing e.g. in potatoes) or as defoliants (e.g. in cotton). They are also suitable for use on fallow land. Other areas of application are tree nurseries, forestry, grassland and ornamental plant growing.
- the active substance combinations can be converted into the customary formulations, such as solutions, emulsions, wettable powders, suspensions, powders, dusts, pastes, soluble powders, granules, suspension emulsion concentrates, active substance-impregnated natural and synthetic substances and very fine encapsulations in polymeric substances.
- formulations are made in a known manner, e.g. by mixing the active ingredients with extenders, that is to say liquid solvents and / or solid carriers, optionally using surface-active agents, that is to say emulsifiers and / or dispersants and / or foam-generating agents.
- extenders that is to say liquid solvents and / or solid carriers
- surface-active agents that is to say emulsifiers and / or dispersants and / or foam-generating agents.
- water is used as an extender, e.g. also organic
- Solvents are used as auxiliary solvents.
- the following are essentially suitable as liquid solvents: aromatics, such as xylene, toluene, or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chlorethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, e.g. Petroleum fractions, mineral and vegetable
- Oils Oils, alcohols such as butanol or glycol and their ethers and esters, ketones such as Acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
- ketones such as Acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone
- strongly polar solvents such as dimethylformamide and dimethyl sulfoxide
- e.g. Ammonium salts and natural rock powders such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic rock powders such as highly disperse silica, aluminum oxide and silicates are suitable as solid carriers for granules: e.g. broken and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules from inorganic and organic flours as well as granules from organic material such as sawdust, coconut shells, corn cobs and tobacco stems; as emulsifying and / or foaming agents are possible: e.g. nonionic and anionic emulsifiers such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, e.g. Alkylaryl polyglycol ethers, alkyl sulfonates,
- Alkyl sulfates, aryl sulfonates and protein hydrolyzates Possible dispersants are: e.g. Lignin sulfate leachate and methyl cellulose.
- Adhesives such as carboxymethyl cellulose, natural and synthetic powdery, granular or latex-shaped polymers, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids such as cephalins and lecithins and synthetic phospholipids can be used in the formulations.
- Other additives can be mineral and vegetable oils.
- Dyes such as inorganic pigments, e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarinv, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc are used.
- inorganic pigments e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarinv, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc are used.
- the formulations generally contain between 0.1 and 95 percent by weight of active ingredients, preferably between 0.5 and 90%.
- the active compound combinations according to the invention are generally used in the form of finished formulations.
- the active substances contained in the active substance combinations can, however, also be mixed in individual formulations when used, that is to say applied in the form of tank mixtures.
- the new combinations of active ingredients can furthermore also be used in a mixture with other known herbicides, ready-to-use formulations or tank mixes being possible.
- a mixture with other known active compounds such as fungicides, insecticides, acaricides, nematicides, bird repellants, growth agents, plant nutrients and agents which improve soil structure, is also possible.
- mineral or vegetable oils which are compatible with plants (e.g. the commercial preparation "Oleo DuPont 11E") or ammonium salts such as e.g. Include ammonium sulfate or ammonium rhodanide.
- the new combinations of active substances can be used as such, in the form of their formulations or in the use forms prepared therefrom by further dilution, such as ready-to-use solutions, suspensions, emulsions, powders, pastes and granules. They are used in the usual way, e.g. by pouring, spraying, spraying, dusting or scattering.
- the active ingredient combinations according to the invention can be applied before and after emergence of the plants, that is to say in the pre-emergence and post-emergence process. They can also be worked into the soil before sowing.
- X % damage by herbicide A (active ingredient of the formula I) at p kg / ha
- Y % damage by herbicide B (active ingredient of the formula II) at q kg / ha
- the effect of the combination is super-additive, that is, it shows a synergistic effect.
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
Priority Applications (12)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05005219.0A EP1552746B1 (fr) | 2000-05-22 | 2001-05-09 | Herbicides sélectifs à base d'hétéroaryloxy-acétamides |
EP10158929A EP2243368A3 (fr) | 2000-05-22 | 2001-05-09 | Herbicides sélectifs à base d'hétéroaryloxy-acetamides |
EP10158916.6A EP2243363B1 (fr) | 2000-05-22 | 2001-05-09 | Herbicides selectifs à base d'heteroaryloxy-acetamides |
EP10158933A EP2243370A2 (fr) | 2000-05-22 | 2001-05-09 | Herbicides sélectifs à base d'hétéroaryloxy-acetamides |
EP10158915.8A EP2243362B1 (fr) | 2000-05-22 | 2001-05-09 | Herbicides selectifs a base d'heteroaryloxy-acetamides |
EP10158932A EP2243369A3 (fr) | 2000-05-22 | 2001-05-09 | Herbicides sélectifs à base d'hétéroaryloxy-acetamides |
EP10158925A EP2243367A3 (fr) | 2000-05-22 | 2001-05-09 | Herbicides sélectifs à base d'hétéroaryloxy-acetamides |
EP10158924A EP2243366A3 (fr) | 2000-05-22 | 2001-05-09 | Herbicides sélectifs à base d'hétéroaryloxy-acetamides |
EP10158913.3A EP2243361B1 (fr) | 2000-05-22 | 2001-05-09 | Herbicides selectifs a base d'heteroaryloxy-acetamides |
DK05005219.0T DK1552746T3 (en) | 2000-05-22 | 2001-05-09 | Selective herbicides based on heteroaryloxy-acetamides |
EP10158918A EP2243365A3 (fr) | 2000-05-22 | 2001-05-09 | Herbicides sélectifs à base d'hétéroaryloxy-acétamides |
EP10158917.4A EP2243364B1 (fr) | 2000-05-22 | 2001-05-09 | Herbicides selectifs a base d'heteroaryloxy-acetamides |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10025306 | 2000-05-22 | ||
DE10025306 | 2000-05-22 | ||
DE10041619A DE10041619A1 (de) | 2000-05-22 | 2000-08-24 | Selektive Herbizide auf Basis von Heteroaryloxyacetamiden |
DE10041619 | 2000-08-24 | ||
PCT/EP2001/005242 WO2001089301A1 (fr) | 2000-05-22 | 2001-05-09 | Herbicides selectifs a base d'heteroaryloxy-acetamides |
Related Child Applications (5)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP10158913.3A Division EP2243361B1 (fr) | 2000-05-22 | 2001-05-09 | Herbicides selectifs a base d'heteroaryloxy-acetamides |
EP10158916.6A Division EP2243363B1 (fr) | 2000-05-22 | 2001-05-09 | Herbicides selectifs à base d'heteroaryloxy-acetamides |
EP10158915.8A Division EP2243362B1 (fr) | 2000-05-22 | 2001-05-09 | Herbicides selectifs a base d'heteroaryloxy-acetamides |
EP05005219.0A Division EP1552746B1 (fr) | 2000-05-22 | 2001-05-09 | Herbicides sélectifs à base d'hétéroaryloxy-acétamides |
EP10158917.4A Division EP2243364B1 (fr) | 2000-05-22 | 2001-05-09 | Herbicides selectifs a base d'heteroaryloxy-acetamides |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1298996A1 true EP1298996A1 (fr) | 2003-04-09 |
Family
ID=26005781
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP01943335A Withdrawn EP1298996A1 (fr) | 2000-05-22 | 2001-05-09 | Herbicides selectifs a base d'heteroaryloxy-acetamides |
Country Status (15)
Country | Link |
---|---|
US (2) | US6967188B2 (fr) |
EP (1) | EP1298996A1 (fr) |
JP (1) | JP2003533545A (fr) |
KR (1) | KR100781758B1 (fr) |
CN (1) | CN1430471A (fr) |
AU (2) | AU6593601A (fr) |
BR (1) | BRPI0111008B1 (fr) |
CA (1) | CA2409215A1 (fr) |
CZ (1) | CZ301614B6 (fr) |
HR (1) | HRP20021022A2 (fr) |
HU (1) | HU230428B1 (fr) |
MX (1) | MXPA02011468A (fr) |
PL (1) | PL218432B1 (fr) |
SK (1) | SK287461B6 (fr) |
WO (1) | WO2001089301A1 (fr) |
Families Citing this family (41)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1209975B1 (fr) * | 1999-09-07 | 2003-11-12 | Syngenta Participations AG | Composition herbicide |
GB0022833D0 (en) | 2000-09-18 | 2000-11-01 | Aventis Cropscience Sa | New herbicidal composition |
AR036047A1 (es) * | 2001-06-13 | 2004-08-04 | Syngenta Participations Ag | Composicion herbicida selectiva y metodo para controlar selectivamente malezas y pastos en cultivos de plantas utiles |
DE10135642A1 (de) * | 2001-07-21 | 2003-02-27 | Bayer Cropscience Gmbh | Herbizid-Kombinationen mit speziellen Sulfonylharnstoffen |
DE10209478A1 (de) * | 2002-03-05 | 2003-09-18 | Bayer Cropscience Gmbh | Herbizid-Kombinationen mit speziellen Sulfonylharnstoffen |
PL371445A1 (en) * | 2002-03-21 | 2005-06-13 | Syngenta Participations Ag | Herbicidal composition |
MY141982A (en) * | 2004-12-21 | 2010-08-16 | Syngenta Participations Ag | Herbicidal composition |
MX2008012995A (es) * | 2006-04-10 | 2008-10-17 | Du Pont | Mezclas herbicidas. |
EP1974609A1 (fr) * | 2007-03-29 | 2008-10-01 | Bayer CropScience GmbH | Procédé de fabrication de granulés dispersibles dans l'eau |
AR069022A1 (es) * | 2007-10-26 | 2009-12-23 | Kumiai Chemical Industry Co | Agente para incrementar el contenido de azucar de la caña de azucar asi como metodo para acelerar la maduracion de la caña de azucar utilizando el mismo |
EP2057898A1 (fr) * | 2007-11-06 | 2009-05-13 | Bayer CropScience AG | Mélanges homogènes et stables de différentes particules granulaires d'agents phytosanitaires |
US20090215625A1 (en) * | 2008-01-07 | 2009-08-27 | Auburn University | Combinations of Herbicides and Safeners |
AU2009214972A1 (en) * | 2008-02-12 | 2009-08-20 | Arysta Lifescience North America, Llc | Method of controlling unwanted vegetation |
JP5563773B2 (ja) * | 2008-12-17 | 2014-07-30 | バイエル・クロップサイエンス・アーゲー | 除草剤組成物 |
DE102008062905A1 (de) * | 2008-12-23 | 2010-06-24 | Saltigo Gmbh | Verfahren zur Herstellung von Acylamid-Verbindungen |
WO2011082968A2 (fr) * | 2009-12-17 | 2011-07-14 | Bayer Cropscience Ag | Agents herbicides contenant du flufénacet |
PL2512249T3 (pl) * | 2009-12-17 | 2016-12-30 | Środki chwastobójcze zawierające flufenacet | |
WO2011082959A2 (fr) | 2009-12-17 | 2011-07-14 | Bayer Cropscience Ag | Agents herbicides contenant du flufénacet |
WO2011082955A2 (fr) * | 2009-12-17 | 2011-07-14 | Bayer Cropscience Ag | Agents herbicides contenant du flufénacet |
HUE030350T2 (en) * | 2009-12-17 | 2017-05-29 | Bayer Ip Gmbh | Herbicidal preparations containing flufenacet |
WO2011082964A1 (fr) | 2009-12-17 | 2011-07-14 | Bayer Cropscience Ag | Produits herbicides contenant du flufénacet |
WO2011082956A2 (fr) | 2009-12-17 | 2011-07-14 | Bayer Cropscience Ag | Agents herbicides contenant du flufénacet |
WO2011082957A2 (fr) * | 2009-12-17 | 2011-07-14 | Bayer Cropscience Ag | Agents herbicides contenant du flufénacet |
WO2011082953A2 (fr) * | 2009-12-17 | 2011-07-14 | Bayer Cropscience Ag | Agents herbicides contenant du flufénacet |
EP2515658B1 (fr) * | 2009-12-17 | 2016-06-08 | Bayer Intellectual Property GmbH | Agents herbicides contenant du flufénacet |
WO2011082954A2 (fr) * | 2009-12-17 | 2011-07-14 | Bayer Cropscience Ag | Agents herbicides contenant du flufénacet |
CN102239854A (zh) * | 2011-05-18 | 2011-11-16 | 利尔化学股份有限公司 | 除草农药组合物 |
WO2014001357A1 (fr) | 2012-06-27 | 2014-01-03 | Bayer Cropscience Ag | Agents herbicides contenant du flufénacet |
WO2014001248A1 (fr) | 2012-06-27 | 2014-01-03 | Bayer Cropscience Ag | Agents herbicides contenant du flufénacet |
WO2014001361A1 (fr) | 2012-06-27 | 2014-01-03 | Bayer Cropscience Ag | Agents herbicides contenant du flufénacet |
HUE042995T2 (hu) | 2012-06-27 | 2019-07-29 | Bayer Cropscience Ag | Flufenacetot tartalmazó herbicid készítmények |
UA116642C2 (uk) | 2012-12-21 | 2018-04-25 | ДАУ АГРОСАЙЄНСІЗ ЕлЕлСі | Термостабільні водні композиції клоквінтосет-мексилу |
WO2014130661A1 (fr) | 2013-02-25 | 2014-08-28 | Dow Agrosciences Llc | Procédés de lutte contre les mauvaises herbes dans des ananas |
PL2967051T3 (pl) | 2013-03-15 | 2019-01-31 | Dow Agrosciences Llc | Synergistyczne zwalczanie chwastów przez nanoszenie penoksulamu i petoksamidu |
EP2936983A1 (fr) | 2014-04-25 | 2015-10-28 | Bayer CropScience AG | Agents actifs destinés à l'augmentation du rendement des cultures de coton |
CN104365628A (zh) * | 2014-11-06 | 2015-02-25 | 江苏省农用激素工程技术研究中心有限公司 | 用于防治大豆田杂草的除草组合物 |
GB2532217B (en) * | 2014-11-11 | 2019-05-15 | Rotam Agrochem Int Co Ltd | Herbicidal composition and method for controlling plant growth |
CN105454266A (zh) * | 2015-12-23 | 2016-04-06 | 汤云鹤 | 一种含氟噻草胺、异丙隆和双氟磺草胺的农药组合物及其在防治小麦田杂草中的应用 |
CN106689141A (zh) * | 2017-03-10 | 2017-05-24 | 合肥星宇化学有限责任公司 | 丙酯草醚和喹禾糠酯复配除草组合物及其制剂和应用 |
CN107751226B (zh) * | 2017-11-27 | 2020-11-13 | 浙江永太药业有限公司 | 一种含哒草特和氟噻草胺的除草剂组合物 |
CN114208833B (zh) * | 2021-12-30 | 2024-03-29 | 青岛润农化工有限公司 | 含氟草烟异辛酯和双氯磺草胺的农药组合物及其制备方法和应用 |
Family Cites Families (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0005501B1 (fr) * | 1978-05-20 | 1981-11-25 | Bayer Ag | Heteroaryloxy-acetamides, procédé pour leur préparation et leur utilisation comme herbicides |
DE3060330D1 (en) * | 1979-04-06 | 1982-06-09 | Bayer Ag | Azolyloxy-acetamides, process for their preparation and their use as herbicides |
DE2946524A1 (de) * | 1979-11-17 | 1981-06-11 | Bayer Ag, 5090 Leverkusen | Azolyloxy-carbonsaeure-n-oxy-amide, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
DE3218482A1 (de) * | 1982-05-15 | 1983-11-17 | Bayer Ag, 5090 Leverkusen | Substituierte 5-trifluormethyl-1,3,4-thiadiazol-2-yloxyessigsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
DE3228147A1 (de) * | 1982-07-28 | 1984-02-09 | Bayer Ag, 5090 Leverkusen | Substituierte 3-trihalogenmethyl-1,2,4-thiadiazol-5-yl-oxyessigsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
DE3228131A1 (de) * | 1982-07-28 | 1984-02-02 | Bayer Ag, 5090 Leverkusen | Substituierte 3-trichlormethyl-1,2,4-thiadiazol-5-yl-oxyessigsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
DE3418168A1 (de) * | 1984-05-16 | 1985-11-21 | Bayer Ag, 5090 Leverkusen | 6-chlorbenzazolyloxyacetamide |
DE3418167A1 (de) | 1984-05-16 | 1985-11-21 | Bayer Ag, 5090 Leverkusen | Verwendung von amiden zur verbesserung der kulturpflanzen-vertraeglichkeit von herbizid wirksamen heteroaryloxyacetamiden |
US4585899A (en) * | 1985-01-22 | 1986-04-29 | Chem Systems Inc. | Hydrogenation of carboxylic acid compounds to aldehydes using MnO2 on gamma alumina as catalyst |
DE3505902A1 (de) * | 1985-02-21 | 1986-08-21 | Bayer Ag, 5090 Leverkusen | 4,5-disubstituierte 1,3-thiazol-2-yloxyacetamide |
DE3811446A1 (de) * | 1988-04-06 | 1989-10-19 | Bodenseewerk Perkin Elmer Co | Einrichtung zur erzeugung eines magnetfeldes in einem atomabsorptions-spektrometer |
DE3821597A1 (de) * | 1988-06-27 | 1989-12-28 | Bayer Ag | 5-difluormethyl-1,3,4-thiadiazol-2-yl- oxyessigsaeureamide, verfahren und 5-difluormethyl-2- methylsulfonyl- bzw. 2- methylthio-1,3,4-thiadiazol als zwischenprodukte zu ihrer herstellung und ihre verwendung als selektivherbizide |
DE3821600A1 (de) * | 1988-06-27 | 1989-12-28 | Bayer Ag | Heteroaryloxyessigsaeure-n-isopropylanilide |
US5529976A (en) * | 1990-01-10 | 1996-06-25 | Hoechst Aktiengesellschaft | Pyridyl sulphonyl ureas as herbicides and plant growth regulators |
DE4223465A1 (de) * | 1992-07-16 | 1994-01-20 | Bayer Ag | Herbizide Mittel auf Basis von Heteroaryloxyacetamiden |
DE4431219A1 (de) * | 1994-09-02 | 1996-03-07 | Bayer Ag | Selektive Herbizide auf Basis von Aryluracilen |
DE4437049A1 (de) * | 1994-10-17 | 1996-04-18 | Bayer Ag | Selektive Herbizide auf Basis von Carbamoyltriazolinonen und Heteroaryloxyacetamiden |
US5912206A (en) * | 1994-12-09 | 1999-06-15 | Rhone-Poulenc Agrochimie | Herbicidal compositions |
DE19546751B4 (de) * | 1994-12-23 | 2005-02-17 | Bayer Cropscience Ag | Selektive Herbizide auf Basis von Heteroaryloxy-acetamiden |
ES2128984B1 (es) * | 1996-05-24 | 2000-02-01 | Bayer Ag | Herbicidas a base de heteroariloxi-acetamidas para el empleo en el cultivo de arroz. |
DE19728568B4 (de) * | 1996-07-17 | 2007-06-14 | Bayer Cropscience Ag | Herbizide Mittel auf Basis von (5-Trifluormethyl-1,3,4-thiadiazol-2-yl-oxy)-essigsäure-N-isopropyl-N-(4fluorphenyl)-amid |
US5985797A (en) * | 1996-07-17 | 1999-11-16 | Bayer Aktiengesellschaft | Herbicidal compositions based on N-isopropyl-N-(4-fluorophenyl) (5-trifluoromethyl-1,3,4-thiadiazol-2-yloxy)acetamide |
DE19634701A1 (de) * | 1996-08-28 | 1998-03-05 | Bayer Ag | Herbizide Mittel auf Basis von 4-Brom-l-methyl-5-trifluormethyl-3-(2-fluor-4-chlor-5-isopropoxycarbonsylphenyl)pyrazol |
AR012651A1 (es) * | 1997-05-06 | 2000-11-08 | Sumitomo Chemical Co | COMPOSICIoN HERBICIDA Y METODO DE DESMALEZADO UTILIZANDO LA MISMA. |
JPH10306007A (ja) * | 1997-05-06 | 1998-11-17 | Sumitomo Chem Co Ltd | 除草剤組成物 |
DE19832017A1 (de) * | 1998-07-16 | 2000-01-27 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel mit substituierten Phenylsulfonylharnstoffen zur Unkrautbekämpfung in Reis |
AU4782099A (en) * | 1998-07-16 | 2000-02-07 | Aventis Cropscience Gmbh | Herbicides |
JP4480890B2 (ja) * | 1998-08-13 | 2010-06-16 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | アシル化アミノフェニルスルホニル尿素を有する除草剤組成物 |
JP4200559B2 (ja) * | 1998-10-23 | 2008-12-24 | 住友化学株式会社 | 除草剤組成物 |
-
2001
- 2001-05-09 AU AU6593601A patent/AU6593601A/xx active Pending
- 2001-05-09 EP EP01943335A patent/EP1298996A1/fr not_active Withdrawn
- 2001-05-09 WO PCT/EP2001/005242 patent/WO2001089301A1/fr not_active Application Discontinuation
- 2001-05-09 MX MXPA02011468A patent/MXPA02011468A/es active IP Right Grant
- 2001-05-09 BR BRPI0111008A patent/BRPI0111008B1/pt active IP Right Grant
- 2001-05-09 KR KR1020027014810A patent/KR100781758B1/ko active IP Right Grant
- 2001-05-09 SK SK1626-2002A patent/SK287461B6/sk not_active IP Right Cessation
- 2001-05-09 US US10/296,006 patent/US6967188B2/en not_active Expired - Lifetime
- 2001-05-09 AU AU2001265936A patent/AU2001265936B2/en not_active Expired
- 2001-05-09 CZ CZ20023822A patent/CZ301614B6/cs not_active IP Right Cessation
- 2001-05-09 CN CN01809989A patent/CN1430471A/zh active Pending
- 2001-05-09 CA CA002409215A patent/CA2409215A1/fr not_active Abandoned
- 2001-05-09 HU HU0302069A patent/HU230428B1/hu unknown
- 2001-05-09 PL PL359033A patent/PL218432B1/pl not_active IP Right Cessation
- 2001-05-09 JP JP2001585555A patent/JP2003533545A/ja active Pending
-
2002
- 2002-12-20 HR HR20021022A patent/HRP20021022A2/xx not_active Application Discontinuation
-
2005
- 2005-08-10 US US11/200,639 patent/US20060009359A1/en not_active Abandoned
Non-Patent Citations (1)
Title |
---|
See references of WO0189301A1 * |
Also Published As
Publication number | Publication date |
---|---|
BR0111008A (pt) | 2003-04-08 |
MXPA02011468A (es) | 2004-08-12 |
HUP0302069A3 (en) | 2005-11-28 |
HRP20021022A2 (en) | 2005-02-28 |
US20040102321A1 (en) | 2004-05-27 |
US6967188B2 (en) | 2005-11-22 |
KR20030027890A (ko) | 2003-04-07 |
AU2001265936B2 (en) | 2006-04-06 |
WO2001089301A1 (fr) | 2001-11-29 |
SK16262002A3 (sk) | 2003-09-11 |
AU6593601A (en) | 2001-12-03 |
KR100781758B1 (ko) | 2007-12-04 |
JP2003533545A (ja) | 2003-11-11 |
CZ301614B6 (cs) | 2010-05-05 |
PL218432B1 (pl) | 2014-12-31 |
HUP0302069A2 (hu) | 2003-09-29 |
CN1430471A (zh) | 2003-07-16 |
SK287461B6 (sk) | 2010-10-07 |
CA2409215A1 (fr) | 2002-11-19 |
BRPI0111008B1 (pt) | 2015-12-15 |
US20060009359A1 (en) | 2006-01-12 |
PL359033A1 (en) | 2004-08-23 |
CZ20023822A3 (cs) | 2003-04-16 |
HU230428B1 (hu) | 2016-06-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2001089301A1 (fr) | Herbicides selectifs a base d'heteroaryloxy-acetamides | |
EP2272353B1 (fr) | Herbicides à base de thien-3-yl-sulfonylamino(thio)carbonyl-triazolin(thi)ones substitués et de dicamba | |
WO2001037652A2 (fr) | Herbicides a base de carbamoyl-triazolinones | |
DE10031825A1 (de) | Selektive Herbizide auf Basis von Arylsulfonylaminocarbonyltriazolinonen | |
EP2243364A2 (fr) | Herbicides sélectifs à base d'hétéroaryloxy-acétamides |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20021223 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR |
|
AX | Request for extension of the european patent |
Extension state: AL LT LV MK RO SI |
|
17Q | First examination report despatched |
Effective date: 20031001 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
RTI1 | Title (correction) |
Free format text: SELECTIVE FLUFENACET-BASED HERBICIDES |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 20050621 |