WO2003024227A2 - Herbicidal composition - Google Patents

Herbicidal composition Download PDF

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Publication number
WO2003024227A2
WO2003024227A2 PCT/EP2002/010541 EP0210541W WO03024227A2 WO 2003024227 A2 WO2003024227 A2 WO 2003024227A2 EP 0210541 W EP0210541 W EP 0210541W WO 03024227 A2 WO03024227 A2 WO 03024227A2
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WO
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Prior art keywords
ethyl
mixture
active ingredient
methyl
picolinafen
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PCT/EP2002/010541
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French (fr)
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WO2003024227A3 (en
Inventor
Georg Rüdiger Kotzian
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Syngenta Participations Ag
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Priority to AU2002342721A priority Critical patent/AU2002342721A1/en
Publication of WO2003024227A2 publication Critical patent/WO2003024227A2/en
Publication of WO2003024227A3 publication Critical patent/WO2003024227A3/en

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N37/00Biocides, 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
    • A01N37/36Biocides, 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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • A01N37/38Biocides, 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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
    • A01N37/40Biocides, 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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/06Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
    • A01N43/10Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with sulfur as the ring hetero atom
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/36Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof

Definitions

  • the present invention relates to a novel herbicidal synergistic composition
  • a novel herbicidal synergistic composition comprising a herbicidal active ingredient combination that is suitable for the selective control of weeds in crops of useful plants, for example in cereal crops.
  • the invention relates also to a method of controlling weeds in crops of useful plants and to the use of the novel composition for that purpose.
  • Mesosulfuron is known from EP-A-559 814 and WO 01/24633, in which the herbicidal activity of this compound is described.
  • a novel synergistic composition for selective weed control which, in addition to comprising customary inert formulation adjuvants, comprises as active ingredient a mixture of at least two compounds selected from the group amidosulfuron, bentazone, bifenox, diflufenican, dicamba, dimethenamid, fenoxaprop-P-ethyl, flurtamone, glufosinate, iodosulfuron-methyl (sodium), bromoxynil, ioxynil, beflubutamid, imazosulfuron, pyraflufen (-ethyl), cinidon-ethyl, 2,4 D, MCPA, MCPP, picolinafen, pendimethalin, imazethapyr, imazapic, imazapyr, imazaquin, imazamox, imazamethabenz-methyl and mesosulfuron, with a mixture of picolin
  • the composition according to the invention can be used against a large number of agronomically important weeds, such as Stellaria, Nasturtium, Agrostis, Digitaria, Avena, Setaria, Sinapis, Lolium, Solanum, Bromus, Apera, Alopecurus, Matricaria, Abutilon, Sida, Xanthium, Amaranthus, Chenopodium, Ipomoea, Chrysanthemum, Galium, Viola and Veronica.
  • the composition according to the invention is suitable for all methods of application conventionally used in agriculture, e.g. pre-emergence application, post-emergence application and seed dressing.
  • composition according to the invention is suitable especially for controlling weeds in crops of useful plants such as cereals and maize and more especially for controlling weeds in cereals.
  • "Crops of useful plants” are to be understood as including those which have been made tolerant to herbicides or classes of herbicides as a result of conventional methods of breeding or genetic engineering.
  • composition according to the invention comprises the said active ingredients in any mixing ratio, but usually has an excess of one component over the other.
  • Preferred mixing ratios of the active ingredients are from 100:1 to 1 :100 and from 50:1 to 1 :50.
  • compositions amidosulfuron + dicamba, bentazone + dicamba, flurtamone + dimethenamid, fenoxaprop-P- ethyl + bromoxynil, fenoxaprop-P-ethyl + ioxynil, glufosinate + dimethenamid, iodosulfuron- methyl (sodium) + dicamba, iodosulfuron-methyl (sodium) + bentazone, iodosulfuron-methyl (sodium) + mesosulfuron, ioxynil + dicamba, ioxynil + bentazone, and ioxynil + mesosulfuron.
  • the mixtures comprising iodosulfuron-methyl (sodium) or mesosulfuron are especially preferred.
  • the rate of application may vary within wide limits and depends on the nature of the soil, the method of application (pre- or post-emergence; seed dressing; application to the seed furrow; no tillage application etc.), the crop plant, the weed to be controlled, the prevailing climatic conditions, and other factors governed by the method of application, the time of application and the target crop.
  • the active ingredient mixture according to the invention can generally be applied at a rate of from 0.001 to 1.5 kg of active ingredient mixture per ha.
  • the mixtures according to the invention may be employed in unmodified form, that is to say as obtained in synthesis.
  • they are formulated in customary manner, together with the adjuvants conventionally used in formulation technology, such as solvents, solid carriers or surfactants, for example into emulsifiable concentrates, directly sprayable or dilutable solutions, wettable powders, soluble powders, dusts, granules or microcapsules, as described in WO 97/34483, pages 9 to 13.
  • the methods of application such as spraying, atomising, dusting, wetting, scattering or pouring, are chosen in accordance with the intended objectives and the prevailing circumstances.
  • the formulations i.e.
  • the media, preparations or compositions comprising the mixtures according to the invention and also, as appropriate, one or more solid or liquid formulation adjuvants, are prepared in a manner known perse, e.g. by intimately mixing and/or grinding the active ingredients with the formulation adjuvants, e.g. solvents or solid carriers.
  • formulation adjuvants e.g. solvents or solid carriers.
  • surface-active compounds surfactants may also be used in the preparation of the formulations.
  • suitable surface-active compounds are non-ionic, cationic and/or anionic surfactants and surfactant mixtures having good emulsifying, dispersing and wetting properties.
  • suitable anionic, non-ionic and cationic surfactants are listed, for example, in WO 97/34485, pages 7 and 8.
  • Also suitable for the preparation of the herbicidal compositions according to the invention are the surfactants conventionally employed in formulation technology, which are described, inter alia, in "McCutcheon's Detergents and Emulsifiers Annual” MC Publishing Corp., Ridgewood New Jersey, 1981 , Stache, H., “Tensid-Taschenbuch", Carl Hanser Verlag, Kunststoff/Vienna, 1981 and M. and J. Ash, "Encyclopedia of Surfactants", Vol l-lll, Chemical Publishing Co., New York, 1980-81.
  • the herbicidal formulations usually contain from 0.1 to 99 % by weight, especially from 0.1 to 95 % by weight, of active ingredient mixture, from 1 to 99.9 % by weight of a solid or liquid formulation adjuvant, and from 0 to 25 % by weight, especially from 0.1 to 25 % by weight, of a surfactant.
  • compositions may also comprise further ingredients, such as stabilisers, e.g. vegetable oils or epoxidised vegetable oils (epoxidised coconut oil, rapeseed oil or soybean oil), antifoams, e.g. silicone oil, preservatives, viscosity regulators, binders, tackifiers and also fertilisers or other active ingredients.
  • stabilisers e.g. vegetable oils or epoxidised vegetable oils (epoxidised coconut oil, rapeseed oil or soybean oil), antifoams, e.g. silicone oil, preservatives, viscosity regulators, binders, tackifiers and also fertilisers or other active ingredients.
  • Emulsifiable concentrates active ingredient mixture: 1 to 90 %, preferably 5 to 20 % surfactant: 1 to 30 %, preferably 10 to 20 % liquid carrier: 5 to 94 %, preferably 70 to 85 %
  • Dusts active ingredient mixture: 0.1 to 10 %, preferably 0.1 to 5 % solid carrier: 99.9 to 90 %, preferably 99.9 to 99 %
  • Suspension concentrates active ingredient mixture: 5 to 75 %, preferably 10 to 50 % water: 94 to 24 %, preferably 88 to 30 % surfactant: 1 to 40 %, preferably 2 to 30 %
  • Wettable powders active ingredient mixture: 0.5 to 90 %, preferably 1 to 80 % surfactant: 0.5 to 20 %, preferably 1 to 15 % solid carrier: 5 to 95 %, preferably 15 to 90 %
  • Granules active ingredient mixture: 0.1 to 30 %, preferably 0.1 to 15 % solid carrier: 99.5 to 70 %, preferably 97 to 85 %
  • Emulsifiable concentrates a) b) c) d) active ingredient mixture 5 % 10% 25% 50% calcium dodecylbenzenesulfonate 6 % 8% 6% 8% castor oil polyglycol ether 4 % - 4% 4%
  • Emulsions of any desired concentration can be obtained from such concentrates by dilution with water.
  • N-methyl-2-pyrrolidone - - 30% 10% arom. hydrocarbon mixture 75 % 60 %
  • the solutions are suitable for use in the form of microdrops.
  • Wettable powders a) b) c) d) active ingredient mixture 5% 25% 50% 80% sodium lignosulfonate 4% - 3% - sodium lauryl sulfate 2% 3% - 4% sodium diisobutylnaphthalene- sulfonate - 6% 5% 6% octylphenol polyglycol ether - 1 % 2% -
  • the active ingredient is mixed thoroughly with the adjuvants and the mixture is thoroughly ground in a suitable mill, affording wettable powders which can be diluted with water to give suspensions of any desired concentration.
  • F4. Coated granules a) b) c) active ingredient mixture 0.1 % 5% 15% highly dispersed silicic acid 0.9 % 2% 2% inorganic carrier 99.0 % 93% 83%
  • the active ingredient is dissolved in methylene chloride and applied to the carrier by spraying, and the solvent is then evaporated off in vacuo.
  • the finely ground active ingredient is uniformly applied, in a mixer, to the carrier moistened with polyethylene glycol.
  • Non-dusty coated granules are obtained in this manner.
  • the active ingredient is mixed and ground with the adjuvants, and the mixture is moistened with water. The mixture is extruded and then dried in a stream of air. F7. Dusts a) b) c) active ingredient mixture 0.1 % 1 % 5% talcum 39.9% 49% 35% kaolin 60.0% 50% 60%
  • Ready-to-use dusts are obtained by mixing the active ingredient with the carriers and grinding the mixture in a suitable mill.
  • Suspension concentrates a) b) c) d) active ingredient mixture 3% 10% 25% 50% ethylene glycol 5% 5% 5% 5% nonylphenol polyglycol ether - 1 % 2 % (15 mol of ethylene oxide) sodium lignosulfonate 3 % 3 % 4 % 5 % carboxymethylcellulose 1 % 1 % 1 % 1 %
  • the finely ground active ingredient is intimately mixed with the adjuvants, giving a suspension concentrate from which suspensions of any desired concentration can be obtained by dilution with water.
  • test plants are sown in pots under greenhouse conditions.
  • a standard soil is used as cultivation substrate.
  • the herbicides are applied to the surface of the soil both alone and in admixture.
  • the rates of application are governed by the optimum concentrations determined under field or greenhouse conditions.
  • test plants are raised to a post-application stage in pots under greenhouse conditions.
  • a standard soil is used as cultivation substrate.
  • the herbicides are applied to the test plants both alone and in admixture.
  • the rates of application are governed by the optimum concentrations determined under field or greenhouse conditions.
  • the mixtures used in this test exhibit good results.

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  • 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

A herbicidal composition which, in addition to comprising customary inert formulation adjuvants, comprises as active ingredient a mixture of at least two compounds selected from the group amidosulfuron, bentazone, bifenox, diflufenican, dicamba, dimethenamid, fenoxaprop-P-ethyl, flurtamone, glufosinate, iodosulfuron-methyl (sodium), bromoxynil, ioxynil, beflubutamid, imazosulfuron, pyraflufen (-ethyl), cinidon-ethyl, 2,4 D, MCPA, MCPP, picolinafen, pendimethalin, imazethapyr, imazapic, imazapyr, imazaquin, imazamox, imazamethabenz-methyl and mesosulfuron, with a mixture of picolinafen and cinidon-ethyl being excluded.

Description

Herbicidal composition
The present invention relates to a novel herbicidal synergistic composition comprising a herbicidal active ingredient combination that is suitable for the selective control of weeds in crops of useful plants, for example in cereal crops.
The invention relates also to a method of controlling weeds in crops of useful plants and to the use of the novel composition for that purpose.
The compounds amidosulfuron, bentazone, bifenox, diflufenican, dicamba, dimethenamid, flurtamone, glufosinate, fenoxaprop-P-ethyl, iodosulfuron-methyl (sodium), bromoxynil, ioxynil, beflubutamid, imazosulfuron, cinidon-ethyl, 2,4 D, MCPA, MCPP, picolinafen, pendimethalin, pyraflufen (-ethyl) and imazethapyr exhibit herbicidal activity, as described, for example, in The Pesticide Manual, 12th Edition (BCPC), 2000. Mesosulfuron is known from EP-A-559 814 and WO 01/24633, in which the herbicidal activity of this compound is described.
Surprisingly, it has now been found that a combination of variable amounts of at least two active ingredients from the above list exhibits a synergistic action that is capable of controlling, both pre-emergence and post-emergence, the majority of weeds occurring especially in crops of useful plants without causing any appreciable damage to the useful plant.
There is therefore proposed in accordance with the present invention a novel synergistic composition for selective weed control which, in addition to comprising customary inert formulation adjuvants, comprises as active ingredient a mixture of at least two compounds selected from the group amidosulfuron, bentazone, bifenox, diflufenican, dicamba, dimethenamid, fenoxaprop-P-ethyl, flurtamone, glufosinate, iodosulfuron-methyl (sodium), bromoxynil, ioxynil, beflubutamid, imazosulfuron, pyraflufen (-ethyl), cinidon-ethyl, 2,4 D, MCPA, MCPP, picolinafen, pendimethalin, imazethapyr, imazapic, imazapyr, imazaquin, imazamox, imazamethabenz-methyl and mesosulfuron, with a mixture of picolinafen and cinidon-ethyl being excluded. It is extremely surprising that combinations of those active ingredients exceed the additive action on the weeds to be controlled that is to be expected in principle and thus broaden the range of action of the two active ingredients especially in two respects: firstly, the rates of application of the individual compounds are reduced while a good level of action is maintained and, secondly, the composition according to the invention achieves a high level of weed control also in those cases where the individual substances, in the range of low rates of application, have become useless from the agronomic standpoint. The result is a considerable broadening of the spectrum of weeds and an additional increase in selectivity in respect of the crops of useful plants, as is necessary and desirable in the event of an unintentional overdose of active ingredient. The composition according to the invention, while retaining excellent control of weeds in useful plants, also allows greater flexibility in succeeding crops.
The composition according to the invention can be used against a large number of agronomically important weeds, such as Stellaria, Nasturtium, Agrostis, Digitaria, Avena, Setaria, Sinapis, Lolium, Solanum, Bromus, Apera, Alopecurus, Matricaria, Abutilon, Sida, Xanthium, Amaranthus, Chenopodium, Ipomoea, Chrysanthemum, Galium, Viola and Veronica. The composition according to the invention is suitable for all methods of application conventionally used in agriculture, e.g. pre-emergence application, post-emergence application and seed dressing. The composition according to the invention is suitable especially for controlling weeds in crops of useful plants such as cereals and maize and more especially for controlling weeds in cereals. "Crops of useful plants" are to be understood as including those which have been made tolerant to herbicides or classes of herbicides as a result of conventional methods of breeding or genetic engineering.
The composition according to the invention comprises the said active ingredients in any mixing ratio, but usually has an excess of one component over the other. Preferred mixing ratios of the active ingredients are from 100:1 to 1 :100 and from 50:1 to 1 :50.
The following combinations have proved to be especially effective compositions: amidosulfuron + dicamba, bentazone + dicamba, flurtamone + dimethenamid, fenoxaprop-P- ethyl + bromoxynil, fenoxaprop-P-ethyl + ioxynil, glufosinate + dimethenamid, iodosulfuron- methyl (sodium) + dicamba, iodosulfuron-methyl (sodium) + bentazone, iodosulfuron-methyl (sodium) + mesosulfuron, ioxynil + dicamba, ioxynil + bentazone, and ioxynil + mesosulfuron. The mixtures comprising iodosulfuron-methyl (sodium) or mesosulfuron are especially preferred. The rate of application may vary within wide limits and depends on the nature of the soil, the method of application (pre- or post-emergence; seed dressing; application to the seed furrow; no tillage application etc.), the crop plant, the weed to be controlled, the prevailing climatic conditions, and other factors governed by the method of application, the time of application and the target crop. The active ingredient mixture according to the invention can generally be applied at a rate of from 0.001 to 1.5 kg of active ingredient mixture per ha.
The mixtures according to the invention may be employed in unmodified form, that is to say as obtained in synthesis. Preferably, however, they are formulated in customary manner, together with the adjuvants conventionally used in formulation technology, such as solvents, solid carriers or surfactants, for example into emulsifiable concentrates, directly sprayable or dilutable solutions, wettable powders, soluble powders, dusts, granules or microcapsules, as described in WO 97/34483, pages 9 to 13. As with the nature of the compositions, the methods of application, such as spraying, atomising, dusting, wetting, scattering or pouring, are chosen in accordance with the intended objectives and the prevailing circumstances. The formulations, i.e. the media, preparations or compositions comprising the mixtures according to the invention and also, as appropriate, one or more solid or liquid formulation adjuvants, are prepared in a manner known perse, e.g. by intimately mixing and/or grinding the active ingredients with the formulation adjuvants, e.g. solvents or solid carriers. In addition, surface-active compounds (surfactants) may also be used in the preparation of the formulations.
Examples of solvents and solid carriers are given, for example, in WO 97/34485, page 6. Depending on the nature of the active ingredients to be formulated, suitable surface-active compounds are non-ionic, cationic and/or anionic surfactants and surfactant mixtures having good emulsifying, dispersing and wetting properties. Examples of suitable anionic, non-ionic and cationic surfactants are listed, for example, in WO 97/34485, pages 7 and 8. Also suitable for the preparation of the herbicidal compositions according to the invention are the surfactants conventionally employed in formulation technology, which are described, inter alia, in "McCutcheon's Detergents and Emulsifiers Annual" MC Publishing Corp., Ridgewood New Jersey, 1981 , Stache, H., "Tensid-Taschenbuch", Carl Hanser Verlag, Munich/Vienna, 1981 and M. and J. Ash, "Encyclopedia of Surfactants", Vol l-lll, Chemical Publishing Co., New York, 1980-81. The herbicidal formulations usually contain from 0.1 to 99 % by weight, especially from 0.1 to 95 % by weight, of active ingredient mixture, from 1 to 99.9 % by weight of a solid or liquid formulation adjuvant, and from 0 to 25 % by weight, especially from 0.1 to 25 % by weight, of a surfactant.
Whereas commercial products are usually formulated as concentrates, the end user will normally employ dilute formulations. The compositions may also comprise further ingredients, such as stabilisers, e.g. vegetable oils or epoxidised vegetable oils (epoxidised coconut oil, rapeseed oil or soybean oil), antifoams, e.g. silicone oil, preservatives, viscosity regulators, binders, tackifiers and also fertilisers or other active ingredients. Preferred formulations have especially the following compositions: (% = percent by weight)
Emulsifiable concentrates: active ingredient mixture: 1 to 90 %, preferably 5 to 20 % surfactant: 1 to 30 %, preferably 10 to 20 % liquid carrier: 5 to 94 %, preferably 70 to 85 %
Dusts: active ingredient mixture: 0.1 to 10 %, preferably 0.1 to 5 % solid carrier: 99.9 to 90 %, preferably 99.9 to 99 %
Suspension concentrates: active ingredient mixture: 5 to 75 %, preferably 10 to 50 % water: 94 to 24 %, preferably 88 to 30 % surfactant: 1 to 40 %, preferably 2 to 30 %
Wettable powders: active ingredient mixture: 0.5 to 90 %, preferably 1 to 80 % surfactant: 0.5 to 20 %, preferably 1 to 15 % solid carrier: 5 to 95 %, preferably 15 to 90 %
Granules: active ingredient mixture: 0.1 to 30 %, preferably 0.1 to 15 % solid carrier: 99.5 to 70 %, preferably 97 to 85 %
The following Examples illustrate the invention further, but do not limit the invention. F1. Emulsifiable concentrates a) b) c) d) active ingredient mixture 5 % 10% 25% 50% calcium dodecylbenzenesulfonate 6 % 8% 6% 8% castor oil polyglycol ether 4 % - 4% 4%
(36 mol of ethylene oxide) octylphenol polyglycol ether - 4 % - 2 %
(7-8 mol of ethylene oxide) cyclohexanone - - 10 % 20 % arom. hydrocarbon mixture 85% 78% 55% 16%
Cg-Cι2
Emulsions of any desired concentration can be obtained from such concentrates by dilution with water.
F2. Solutions a) b) c) d) active ingredient mixture 5% 10% 50% 90%
1 -methoxy-3-(3-methoxy- propoxy)-propane - 20% 20% - polyethylene glycol MW 400 20% 10% _ _
N-methyl-2-pyrrolidone - - 30% 10% arom. hydrocarbon mixture 75 % 60 %
The solutions are suitable for use in the form of microdrops.
F3. Wettable powders a) b) c) d) active ingredient mixture 5% 25% 50% 80% sodium lignosulfonate 4% - 3% - sodium lauryl sulfate 2% 3% - 4% sodium diisobutylnaphthalene- sulfonate - 6% 5% 6% octylphenol polyglycol ether - 1 % 2% -
(7-8 mol of ethylene oxide) highly dispersed silicic acid 1 % 3% 5% 10% kaolin 88% 62% 35% -
The active ingredient is mixed thoroughly with the adjuvants and the mixture is thoroughly ground in a suitable mill, affording wettable powders which can be diluted with water to give suspensions of any desired concentration. F4. Coated granules a) b) c) active ingredient mixture 0.1 % 5% 15% highly dispersed silicic acid 0.9 % 2% 2% inorganic carrier 99.0 % 93% 83%
(diameter 0.1 - 1 mm) e.g. CaCO3 or SiO2
The active ingredient is dissolved in methylene chloride and applied to the carrier by spraying, and the solvent is then evaporated off in vacuo.
F5. Coated granules a) b) c) active ingredient mixture 0.1 % 5% 15% polyethylene glycol MW 200 1.0% 2% 3% highly dispersed silicic acid 0.9 % 1 % 2% inorganic carrier 98.0 % 92% 80%
(diameter 0.1 - 1 mm) e.g. CaCO3 or SiO2
The finely ground active ingredient is uniformly applied, in a mixer, to the carrier moistened with polyethylene glycol. Non-dusty coated granules are obtained in this manner.
F6. Extruder granules a) b) c) d) active ingredient mixture 0.1 % 3% 5% 15% sodium lignosulfonate 1.5% 2% 3% 4% carboxymethylcellulose 1.4% 2% 2% 2% kaolin 97.0 % 93% 90% 79%
The active ingredient is mixed and ground with the adjuvants, and the mixture is moistened with water. The mixture is extruded and then dried in a stream of air. F7. Dusts a) b) c) active ingredient mixture 0.1 % 1 % 5% talcum 39.9% 49% 35% kaolin 60.0% 50% 60%
Ready-to-use dusts are obtained by mixing the active ingredient with the carriers and grinding the mixture in a suitable mill.
F8. Suspension concentrates a) b) c) d) active ingredient mixture 3% 10% 25% 50% ethylene glycol 5% 5% 5% 5% nonylphenol polyglycol ether - 1 % 2 % (15 mol of ethylene oxide) sodium lignosulfonate 3 % 3 % 4 % 5 % carboxymethylcellulose 1 % 1 % 1 % 1 %
37 % aqueous formaldehyde 0.2 % 0.2 % 0.2 % 0.2 % solution silicone oil emulsion 0.8 % 0.8 % 0.8 % 0.8 % water 87 % 79 % 62 % 38 %
The finely ground active ingredient is intimately mixed with the adjuvants, giving a suspension concentrate from which suspensions of any desired concentration can be obtained by dilution with water.
It is often more practical for the active ingredients of the mixtures according to the invention to be formulated separately and to be brought together in the desired mixing ratio in the applicator in the form of a "tank mixture" in water shortly before application.
Biological Examples:
Example B1 : Pre-emergence test:
The test plants are sown in pots under greenhouse conditions. A standard soil is used as cultivation substrate. At a pre-emergence stage the herbicides are applied to the surface of the soil both alone and in admixture. The rates of application are governed by the optimum concentrations determined under field or greenhouse conditions. The tests are evaluated 2 to 4 weeks later (100% action = plant has completely died; 0% action = no phytotoxic action).
The mixtures used in this test exhibit good results.
Example B2: Post-emergence test:
The test plants are raised to a post-application stage in pots under greenhouse conditions. A standard soil is used as cultivation substrate. At a post-emergence stage the herbicides are applied to the test plants both alone and in admixture. The rates of application are governed by the optimum concentrations determined under field or greenhouse conditions. The tests are evaluated 2 to 4 weeks later (100% action = plant has completely died; 0% action = no phytotoxic action). The mixtures used in this test exhibit good results.

Claims

What is claimed is:
1. A herbicidal synergistic composition which, in addition to comprising customary inert formulation adjuvants, comprises as active ingredient a mixture of at least two compounds selected from the group amidosulfuron, bentazone, bifenox, diflufenican, dicamba, dimethenamid, fenoxaprop-P-ethyl, flurtamone, glufosinate, iodosulfuron-methyl (sodium), bromoxynil, ioxynil, beflubutamid, imazosulfuron, pyraflufen (-ethyl), cinidon-ethyl, 2,4 D, MCPA, MCPP, picolinafen, pendimethalin, imazethapyr, imazapic, imazapyr, imazaquin, imazamox, imazamethabenz-methyl and mesosulfuron, with a mixture of picolinafen and cinidon-ethyl being excluded.
2. A method of controlling undesired plant growth in crops of useful plants, which comprises allowing a herbicidally effective amount of a composition according to claim 1 to act on the crop plant or the locus thereof.
3. A method according to claim 2, wherein the crop plant is a cereal.
PCT/EP2002/010541 2001-09-20 2002-09-19 Herbicidal composition WO2003024227A2 (en)

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CN101971824A (en) * 2010-11-09 2011-02-16 上海生农生化制品有限公司 Fenoxaprop-p-ethyl and dicamba composition and application thereof
CN102027910A (en) * 2009-09-28 2011-04-27 南京华洲药业有限公司 Herbicidal composition containing diflufenican and dicamba and application thereof
CN102027940A (en) * 2009-09-28 2011-04-27 南京华洲药业有限公司 Herbicidal composition containing diflufenican and fenoxaprop-ethyl and application thereof
CN102258028A (en) * 2011-07-06 2011-11-30 陕西美邦农药有限公司 Weeding composition containing beflubutamid and pyraflufen-ethyl
CN102265872A (en) * 2010-06-07 2011-12-07 南京华洲药业有限公司 Weeding composition containing bentazone, dicamba and mesotrione, and application thereof
CN102326551A (en) * 2011-07-11 2012-01-25 陕西美邦农药有限公司 Weeding composition containing diflufenican
CN102334483A (en) * 2011-07-19 2012-02-01 陕西美邦农药有限公司 Weeding composition containing beflubutamid and terbutryn
EP2677859A2 (en) * 2011-02-22 2014-01-01 Dow AgroSciences LLC Methods of weed control involving aad-1 plants, and re-plant and/or pre-emergence herbicide applications
CN104304294A (en) * 2014-09-12 2015-01-28 青岛润鑫伟业科贸有限公司 Mulberry garden herbicide and preparation method thereof
CN104381280A (en) * 2014-11-12 2015-03-04 济南凯因生物科技有限公司 Emulsifiable concentrate preparation of herbicide
US10323287B2 (en) 2009-08-19 2019-06-18 Dow Agrosciences Llc AAD-1 event DAS-40278-9, related transgenic corn lines, and event-specific identification thereof
WO2019215613A1 (en) 2018-05-07 2019-11-14 Adama Agan Ltd. Stable phytoene desaturase inhibitor herbicide formulation
CN111387190A (en) * 2020-05-10 2020-07-10 辽宁山水益农科技有限公司 Weeding composition containing dicamba and bentazone

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US11098322B2 (en) 2009-08-19 2021-08-24 Dow Agrosciences Llc AAD-1 event DAS-40278-9, related transgenic corn lines, and event-specific identification thereof
US10323287B2 (en) 2009-08-19 2019-06-18 Dow Agrosciences Llc AAD-1 event DAS-40278-9, related transgenic corn lines, and event-specific identification thereof
CN102027940B (en) * 2009-09-28 2013-09-18 南京华洲药业有限公司 Herbicidal composition containing diflufenican and fenoxaprop-ethyl and application thereof
CN102027940A (en) * 2009-09-28 2011-04-27 南京华洲药业有限公司 Herbicidal composition containing diflufenican and fenoxaprop-ethyl and application thereof
CN102027910A (en) * 2009-09-28 2011-04-27 南京华洲药业有限公司 Herbicidal composition containing diflufenican and dicamba and application thereof
CN102265872A (en) * 2010-06-07 2011-12-07 南京华洲药业有限公司 Weeding composition containing bentazone, dicamba and mesotrione, and application thereof
CN101971824A (en) * 2010-11-09 2011-02-16 上海生农生化制品有限公司 Fenoxaprop-p-ethyl and dicamba composition and application thereof
RU2610664C2 (en) * 2011-02-22 2017-02-14 ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи Method of controlling weeds using plants aad-1 and presowing and / or pre-emergence treatment with herbicides
EP2677859A2 (en) * 2011-02-22 2014-01-01 Dow AgroSciences LLC Methods of weed control involving aad-1 plants, and re-plant and/or pre-emergence herbicide applications
EP2677859A4 (en) * 2011-02-22 2015-04-15 Dow Agrosciences Llc Methods of weed control involving aad-1 plants, and re-plant and/or pre-emergence herbicide applications
AP3980A (en) * 2011-02-22 2017-01-05 Dow Agrosciences Llc Methods of weed control involving aad-1 plants, and re-plant and/or pre-emergence herbicide applications
CN102258028A (en) * 2011-07-06 2011-11-30 陕西美邦农药有限公司 Weeding composition containing beflubutamid and pyraflufen-ethyl
CN102258028B (en) * 2011-07-06 2014-08-13 陕西美邦农药有限公司 Weeding composition containing beflubutamid and pyraflufen-ethyl
CN102326551A (en) * 2011-07-11 2012-01-25 陕西美邦农药有限公司 Weeding composition containing diflufenican
CN102334483B (en) * 2011-07-19 2014-03-19 陕西美邦农药有限公司 Weeding composition containing beflubutamid and terbutryn
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CN104304294A (en) * 2014-09-12 2015-01-28 青岛润鑫伟业科贸有限公司 Mulberry garden herbicide and preparation method thereof
CN104381280A (en) * 2014-11-12 2015-03-04 济南凯因生物科技有限公司 Emulsifiable concentrate preparation of herbicide
WO2019215613A1 (en) 2018-05-07 2019-11-14 Adama Agan Ltd. Stable phytoene desaturase inhibitor herbicide formulation
EP3915370A1 (en) 2018-05-07 2021-12-01 Adama Agan Ltd. Stable phytoene desaturase inhibitor herbicide formulation
CN111387190A (en) * 2020-05-10 2020-07-10 辽宁山水益农科技有限公司 Weeding composition containing dicamba and bentazone

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