WO2005046328A1 - Nanopartikuläre wirkstoffformulierungen - Google Patents
Nanopartikuläre wirkstoffformulierungen Download PDFInfo
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- WO2005046328A1 WO2005046328A1 PCT/EP2004/011797 EP2004011797W WO2005046328A1 WO 2005046328 A1 WO2005046328 A1 WO 2005046328A1 EP 2004011797 W EP2004011797 W EP 2004011797W WO 2005046328 A1 WO2005046328 A1 WO 2005046328A1
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- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
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- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/08—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing solids as carriers or diluents
- A01N25/10—Macromolecular compounds
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- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
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- 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
- A01N47/00—Biocides, 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
- A01N47/08—Biocides, 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
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- 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
- A01N47/00—Biocides, 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
- A01N47/08—Biocides, 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1804—C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/52—Amides or imides
- C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F220/58—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing oxygen in addition to the carbonamido oxygen, e.g. N-methylolacrylamide, N-(meth)acryloylmorpholine
- C08F220/585—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing oxygen in addition to the carbonamido oxygen, e.g. N-methylolacrylamide, N-(meth)acryloylmorpholine and containing other heteroatoms, e.g. 2-acrylamido-2-methylpropane sulfonic acid [AMPS]
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/30—Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety
- C08F220/301—Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety and one oxygen in the alcohol moiety
Definitions
- the present invention relates to active substance formulations which, in addition to at least one active substance, contain at least one random radical copolymer which, as monomer units, contains at least one olefinically unsaturated sulfonic acid i or a salt thereof or a mixture of acid and salt, at least one alkyl, aryl, alkylaryl, arylalkyl-, aryloxyalkyl-, alkoxyaryl- or hydroxyalkyl-substituted.es (meth) acrylate or (meth) acrylamide ii and optionally further additives.
- the invention further relates to processes for the preparation of the active substance formulations, dispersions which are prepared by redispersing these active substance formulations in aqueous systems and the use of these active substance formulations.
- active ingredients are ideally provided in the form of aqueous systems. This naturally complicates the effective use of active ingredients which are insoluble or only slightly soluble in water, since the bioavailability and thus the biological activity are low. Many active ingredients, especially in the agricultural and pharmaceutical sectors, are hydrophobic in nature and are therefore subject to the application problem mentioned.
- solubility, dispersibility and bioavailability of active ingredient particles can be increased by increasing the particle surface, that is to say by reducing the particle size, for the same total amount. For example, the penetration of biological membranes with a smaller particle size is simplified. At the same time, this means that compared to the use of the active ingredient in the form of larger particles, the amounts of active ingredient required when using particles are smaller in the size range of one micrometer and less to achieve the same effect.
- Typical stabilizers are low molecular weight surfactants or oligomers that lead to micelle formation.
- the often low active substance content of such micelles is disadvantageous.
- higher molecular weight aids such as colloids, amphiphilic polymers and thickeners also enable small particles of active substance to be stabilized.
- WO 97/13503 discloses a method for producing nanoparticles in which an agent and a matrix are brought together in solution and then represented in a spray drying step as nanocomposite powder, which can be redispersed in an aqueous medium.
- the nanoparticles produced in this way are smaller than 5000 nm, particularly preferably smaller than 250 nm.
- pesticides are also mentioned as possible applications.
- Carbohydrates, proteins, inorganic salts, resins or lipids are mentioned as matrix materials, gelatin, starch, polyvinylpyrrolidone, arabinogalactan, polyvinyl alcohol, polyacrylic acid, polyethylene, polymethacrylates, polyamide, poly-
- EP-A 0275796 discloses a process for the production of colloidally dispersible systems by the formation of spherical nanoparticles.
- the method comprises dissolving a first component A in a solvent or solvent mixture, optionally adding surfactants, and providing a second solvent or solvent mixture, the second solvent or solvent mixture not dissolving component A.
- Surface-active substances are optionally added to the second solvent or solvent mixture and the second solvent / solvent mixture is miscible in any ratio with the solvent / solvent mixture of component A.
- nanoparticles are formed which are smaller than 500 nm.
- Possible components A are polymers, fats, fatty acid esters, biologically active substances, pigments, lubricants or colorants.
- WO 98/16105 discloses solid crop protection agents, consisting essentially of one or more predominantly amorphous, inherently solid crop protection agents with a water solubility of less than 500 mg / l at 25 ° C. and a coating layer surrounding the active ingredients.
- the preparation of the agent is carried out by mixing a liquid formulation of the crop protection active ingredient with a liquid formulation of a wrapping material and drying the crop protection active ingredient coated in this way.
- Preferred solvents are volatile, water-miscible solvents.
- the dried nanoparticles can be redispersed in aqueous media, the particle sizes are 0.1 to 0.8 micrometers.
- Suitable surface layer materials are surface-active or surface-active polymeric colloids or oligomeric, amphiphilic compounds or mixtures thereof.
- Biopolymers and modified biopolymers are preferably used. Synthetic anionic and neutral polymers, such as polyvinyl alcohol, polyvinyl pyrrolidone and polyacrylic acid, are also suitable.
- WO 03/039249 relates to a solid crop protection formulation comprising a crop protection agent and a randomly radical copolymer which contains at least one hydrophilic and one hydrophobic monomer as polymerized units and, optionally, further additives. In the aqueous dispersion described, at least 50% of the dispersed particles are in an X-ray amorphous state.
- Procationic nitrogen-containing compounds such as vinyl-substituted pyridines or aminoalkyl-substituted (meth) acrylamides are used as hydrophilic monomers.
- EP-A 0 875 143 discloses pesticide compositions with a polymer content of 0.01 to 40% by weight, in which at least one of the components is a polymer which lowers the crystallization of the pesticide active ingredient of the composition.
- the polymers can be lipophilic or both lipophilic and hydrophilic in character.
- the hydrophilic character is determined by monomer units which are selected from substituted alkyl esters, alkyl thioesters and mono- or dialkylamides of monoethylenically unsaturated monomers such as acrylic, methacrylic, fumaric, maleic and itaconic acids, substituted or unsubstituted vinyl esters of CrC 4 carboxylates, cyclic esters, amides and heterocycles and vinyl substituted amines.
- the polymers are given the lipophilic character by ethylenically unsaturated monomers such as long-chain alkyl esters and mono- or disubstituted alkylamides of acrylic acid, methacrylic acid, fumaric acid, maleic acid or itaconic acid, by .alpha.-olefins or vinyl alcohol esters, vinyl halides, vinyl nitriles and vinyl carboxylates.
- ethylenically unsaturated monomers such as long-chain alkyl esters and mono- or disubstituted alkylamides of acrylic acid, methacrylic acid, fumaric acid, maleic acid or itaconic acid, by .alpha.-olefins or vinyl alcohol esters, vinyl halides, vinyl nitriles and vinyl carboxylates.
- WO 02/082900 describes aqueous suspensions of nanoparticles.
- the nanoparticles are composed of an amphiphilic compound with at least one hydrophobic and at least one hydrophilic unit and at least 50 percent by weight of an organic, water-insoluble agrochemical substance per 100 parts of the amphiphilic compound.
- Amphiphilic diblock copolymers are disclosed as phase mediators.
- DE-A 10151392 describes powdered active ingredient formulations which consist of a biological active ingredient, a dispersant, polyvinyl alcohol and optionally additives.
- the active ingredient and the dispersing agent are suspended in the aqueous phase and heated to the melt, an emulsion is formed.
- This emulsion is homogenized with a jet disperser and then quickly cooled until the dispersed melt solidifies.
- the finely divided dispersion is then mixed with aqueous polyvinyl alcohol solution, as a result of which a film of polyvinyl alcohol enclosing the dispersion particles is formed.
- EP-A 0875 142 discloses dispersions of crop protection agents in agricultural oils and a method for producing these dispersions.
- the size of the dispersed particles is between 0.5 and 10 micrometers.
- the polymers that are used Dispersion of the active ingredients are used, 2.5 to 35 wt .-% consist of polar monomers.
- Monomers bearing hydroxyl, carboxylic acid and nitrogen groups are used as polar monomers.
- Preferred monomers are long-chain (meth) acrylates and, as the polar monomer, dimethylaminopropyl methacrylamide (DMAPMA).
- the object of the present invention was to provide new possibilities for the formulation of active substances, in particular for the nanodispersion of active substances which are intrinsically difficult to dissolve in an aqueous medium.
- the present invention relates to active substance formulations comprising a. at least one active ingredient, b. at least one random radical copolymer containing at least one olefinically unsaturated sulfonic acid of the formula I as monomers
- X oxygen or NR 5
- R 1 is hydrogen or methyl
- n can have a value from 0 to 10 and R 2 and R 3 independently of one another are C to C 6 alkyl
- R 5 is hydrogen, alkyl, aryl, alkylaryl, arylalkyl, Alkoxyalkyl, aryloxyalkyl, alkoxyaryl, hydroxyalkyl, (di) alkylaminoalkyl, (di) alkylaminoaryl, (di) arylaminoalkyl, alkylarylaminoalkyl, alkylarylaminoaryl, where the aryl radicals can be substituted, and the olefinic unsaturated sulfonic acid in acid or salt form or as a mixture of acid and salt form can be present, at least one olefinically unsaturated monomer of formula II
- R 5 and R 6 are independently hydrogen, alkyl, aryl, alkylaryl, arylalkyl, alkoxyalkyl, aryloxyalkyl, alkoxyaryl, hydroxyalkyl, (di) alkylaminoalkyl, (di) alkylaminoaryl, (di ) Arylaminoalkyl, alkylarylaminoalkyl, alkylarylaminoaryl, optionally further monomers and c. optionally other additives.
- Salts of the sulfonic acid of the formula I are preferably alkali or ammonium salts.
- C 1 -C 20 -Alkyl are suitable as alkyl radicals alone or in the combinations mentioned.
- C 6 to C 6 alkyl such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2- Dimethylbutyl, 1, 3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 1, 2-trimethylpropyl, 1,
- Aryl radicals are taken to mean mono- or polynuclear, optionally substituted aromatic hydrocarbon radicals. Examples include phenyl, naphthyl or phenyl substituted by halogen such as fluorine or chlorine.
- Alkoxy stands for an alkyl radical that is attached to the skeleton via an oxygen atom (-O-).
- Aryloxy stands for an aryl radical which is bonded to the skeleton via an oxygen atom (-O-).
- vinyl aromatic monomers such as styrene and styrene derivatives such as ⁇ -methylstyrene, vinyl toluene, ortho-, meta- and para-methyl styrene, ethyl vinyl benzene, vinyl naphthalene, vinyl xylene and the corresponding halogenated vinyl aromatic monomers, nitro, alkoxy, haloalkyl, vinyl aromatic monomers carrying carbalkoxy, carboxy, amino and alkylamino groups, ⁇ -olefins such as ethene, propene, 1-butene, 1-pentene, 1-hexene, isobutene, long-chain (C 10 - C 2 o) alkyl- ⁇ -olefins , Dienes such as butadiene and isoprene, vinyl alcohol esters such as vinyl acetate, vinyl halides such as vinyl chloride, vinyl bromide, vinyl fluoride, vinylidene chlor
- a polymer referred to as “radical” is understood as a polymer produced by radical polymerization.
- a “statistical” copolymer is understood to mean a copolymer in which the monomer sequence is determined by the copolymerization parameters of the monomers. The same also applies to copolymers consisting of more than two types of monomers. This type of polymer is also referred to as a random copolymer.
- suifonic acids of the formula I can be in acid or salt form or as a mixture of acid and salt form.
- sulfonic acid is used to represent all of these forms.
- Salts of sulfonic acid are metal salts, especially alkali metal salts such as lithium, sodium or potassium salts or ammonium salts.
- the random radical copolymer according to the invention contains as monomers at least one olefinically unsaturated sulfonic acid of the formula I, at least one (meth) acrylate of the formula IIa
- R 4 is hydrogen or methyl and R 7 , R 8 and R 9 are independently hydrogen, C t to C 6 alkyl, halogen, hydroxy, Ci to C 6 -alkoxy, where alkyl and alkoxy may be halogen-substituted, and optionally further olefinic monomers of the formula Mb
- YO or NR 5 , R 10 is hydrogen or methyl
- R 5 , R 6 is hydrogen, alkyl, aryl, alkylaryl, arylalkyl, alkoxyalkyl, aryloxyalkyl, alkoxyaryl, hydroxyalkyl, (di) alkylaminoalkyl, (di) alkylaminoaryl, (di) arylaminoalkyl, Alkylarylaminoalkyl, alkylarylaminoaryl, where the aryl radicals can be substituted.
- Alkoxy is an alkyl radical as mentioned above which is bonded to the skeleton via an oxygen atom.
- Aryloxy stands for an aryl radical which is bonded to the skeleton via an oxygen atom (-O-).
- Aryl radicals are taken to mean mono- or polynuclear, optionally substituted aromatic hydrocarbon radicals. Examples include phenyl, naphthyl or phenyl substituted by halogen such as fluorine or chlorine.
- Aryloxy stands for an aryl radical as mentioned above, which is bonded to the skeleton via an oxygen atom.
- alkylaryl for tolyl
- arylalkyl for benzyl
- alkoxyalkyl for ethoxyethyl
- aryloxyalkyl for phenoxyethyl
- alkoxyaryl for methoxyphenyl
- hydroxyalkyl for hydroxyethyl
- alkylaminoalkyl for dimethylaminopropyl.
- the random radical copolymer according to the invention is composed of at least one olefinically unsaturated sulfonic acid of the formula I and phenoxy-C 6 alkyl acrylate such as, for example, phenoxyethyl acrylate.
- the random radical copolymer is composed of monomers of the above formula I, in particular 2-acrylamido-2-methyl-1-propanesulfonic acid and at least one olefinically unsaturated monomer of the formula II
- Y is oxygen or NR 5 , R 4 is hydrogen or methyl, R ⁇ , R 6 is hydrogen, alkyl, aryl, alkylaryl, arylalkyl, alkoxyalkyl, aryloxyalkyl, alkoxyaryl, hydroxyalkyl, (di) alkylaminoalkyl, (di) alkylaminoaryl, (di) Arylaminoalkyl, alkylarylaminoalkyl, alkylarylaminoaryl, where alkyl and aryl have the meanings given above, and optionally further monomers.
- the statistical radical copolymer contains 2-acrylamido-2-methyl-1-propanesulfonic acid as monomers and at least one olefinically unsaturated monomer of the formula II, where Y is oxygen, R 4 is hydrogen and R 6 is hydrogen or alkyl , Accordingly, the statistical radical copolymer in this particularly preferred embodiment contains 2-acrylamido-2-methyl-1-propanesulfonic acid as monomers and at least one ester of acrylic acid.
- esters of acrylic acid are, for example, methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, butyl acrylate, 2-methylpropyl acrylate, tert-butyl acrylate, hexyl acrylate, cyclohexyl acrylate, n-octyl acrylate, 2-ethylhexyl acrylate, undylecyl acrylate, decyl acrylate, decyl acrylate, Myristyl acrylate, pentadecyl acrylate, cetyl acrylate, heptadecyl acrylate, stearyl acrylate.
- the random radical copolymer contains 2-acrylamido-2-methyl-1-propanesulfonic acid, phenoxyethyl acrylate and at least one ester of acrylic acid as monomers.
- the random radical copolymer is composed of the monomers 2-acrylamido-2-methyl-1-propanesulfonic acid and phenoxyethyl acrylate.
- the molecular weights M w and M n and the non-uniformity of the polymers are determined by size exclusion chromatography. Standard PMMA calibration sets can be used as calibration material.
- the percentage of the at least one olefinically unsaturated sulfonic acid in the total mass of the at least one randomly radical copolymer is 10 to 90, preferably 20 to 80 and particularly preferably 30 to 70 percent by weight.
- the statistical radical copolymers according to the invention are preferably synthesized in the usual way by free radical polymerization. However, others, e.g. controlled radical processes for polymerization are used.
- the polymerization is carried out in the presence of the monomers and one or more initiators and can be carried out with or without solvent, in emulsion or in suspension.
- the polymerization can be carried out as a batch reaction, in a semi-continuous or continuous procedure.
- the reaction times are generally between 1 and 12 hours.
- the temperature range in which the reactions can be carried out generally ranges from 20 to 200 ° C., preferably from 40 to 120 ° C.
- Usual radical-forming substances are used as initiators for the radical polymerization.
- the initiator is preferably selected from the group of azo compounds, peroxide compounds or hydroperoxide compounds. Examples include acetyl peroxide, benzoyl peroxide, lauroyl peroxide, tert-butyl peroxy isobutyrate, caproyl peroxide, cumene hydroperoxide, azobisisobutyronitrile or 2,2-azobis (2-methylbutane) nitrile. Azobisisobutyronitrile (AIBN) is particularly preferred.
- the radical polymerization is preferably carried out in solution.
- Solvents are water, alcohols such as methanol, ethanol, isopropanol, dipolar aprotic solvents such as DMF, DMSO or NMP, aromatic, aliphatic, halogenated or unhalogenated hydrocarbons such as hexane, chlorobenzene, toluene or benzene.
- Preferred solvents are isopropanol, methanol, toluene, DMF, NMP, DMSO and hexane, and DMF is particularly preferred.
- the ratio of the proportions by weight of active ingredient (s) to randomly radical copolymer (s) is in the range from 1:10 to 10: 1, preferably in the range from 1: 4 to 4: 1, particularly preferably in the range from 1 : 2 to 2: 1.
- Active substances within the meaning of the present invention are preferably poorly water-soluble active substances such as biologically or pharmaceutically active compounds, but also poorly water-soluble effect substances such as colorants, fragrances, flavors and active substances and effect substances used in cosmetics.
- Slightly water-soluble means a water solubility of less than 1000 mg / l, preferably less than 100 mg / l each at a temperature of 20 ° C.
- the invention preferably relates to the formulation of crop protection active ingredients, the production of dispersants of these crop protection formulations and agents and processes for controlling pests and undesirable plant growth by using the crop protection formulation according to the invention.
- Fungicides bactericides, insecticides, acaricides, nematocides, molluscicides, herbicides and plant growth regulators may be mentioned as crop protection agents.
- Preferred crop protection agents are herbicides, acaricides, insecticides, nematicides and fungicides, which are listed at http://www.hclrss.demon.co.uk/index_cn_frame.html (Index of common names).
- the following herbicides, acaricides, insecticides, nematicides and fungicides may be mentioned, for example:
- Particularly preferred crop protection agents are fungicides, such as, for example
- Acylalanines such as benalaxyl, metalaxyl, ofurace, oxadixyl,
- Amine derivatives such as aldimorph, dodine, dodemorph, fenpropimorph, fenpropidine, guazatine, iminoctadine, spiroxamine, tridemorph, • anilinopyrimidines such as pyrimethanil, mepanipyrim or cyrodinyl,
- Antibiotics such as cycloheximide, griseofuivin, kasugamycin, natamycin, polyoxin or streptomycin,
- azoles such as bitertanol, bromoconazole, cyproconazole, difenoconazole, Dinitrocona- zol, epoxiconazole, fenbuconazole, Fluquiconazol, flusilazole, hexaconazole, Imaza- lil, metconazole, myclobutanil, penconazole, propiconazole, prochloraz, Prothioco- Nazole, tebuconazole, triadimefon, triadimenol, triflumizole , Triticonazole,
- Dicarboximides such as iprodione, myclozolin, procymidone, vinclozolin,
- Dithiocarbamates such as Ferbam, Nabam, Maneb, Mancozeb, Metam, Metiram, Propinerb, Polycarbamate, Thiram, Ziram, Zineb, • Heterocyclic compounds such as anilazine, benomyl, boscalid, carbendazim, carboxin, oxycarboxin, cyazofamide, dazonam, fazonet, dazomet , Fenamidon, fenarimol, fuberidazole, flutoianil, furametpyr, isoprothiolan, mepronil, nuanimolol, probenazole, proquinazide, pyrifenox, pyroquilone, quinoxyfen, silthiofam, thiabendazole, thifluzamide, thiophanate, triizinol, triadinol, triadinol, triadinol, triadinol, triadinol, tria
- Nitrophenyl derivatives such as binapacryl, dinocap, dinobutone, nitrophthal-isopropyl,
- Phenylpyrroles such as fenpiclonil or fludioxonil
- Cinnamic acid amides and analogues such as dimethomorph, flumetover or flumorph.
- strobilurins such as azoxystrobin, dimoxystrobin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyracostrobin or trif loxystrobin, in particular pyraclostrobin, are very particularly preferred.
- a plurality of crop protection active ingredients - including different indications - can be present side by side.
- a preferred crop protection formulation contains as component a. at least one crop protection agent selected from the class of fungicides.
- Active substance formulations in which the at least one active substance is selected from the group of strobilurins are particularly preferred, pyraclostrobin being particularly preferred.
- Active ingredient formulations which contain mixtures of pyraclostrobin with further crop protection active ingredients as active ingredient are furthermore particularly preferred.
- Such mixing partners are • acylalanines such as benalaxyl, metalaxyl, ofurace, oxadixyl,
- Amine derivatives such as aldimorph, dodine, dodemorph, fenpropimorph, fenpropidin, guazatine, iminoctadine, spiroxamine, tridemorph,
- Anilinopyrimidines such as pyrimethanil, mepanipyrim or cyrodinyl,
- Antibiotics such as cycloheximide, griseofulvin, kasugamycin, natamycin, polyoxin or streptomycin,
- azoles such as bitertanol, bromoconazole, cyproconazole, difenoconazole, Dinitrocona- zol, epoxiconazole, fenbuconazole, Fluquiconazol, flusilazole, hexaconazole, Imaza- lil, metconazole, myclobutanil, penconazole, propiconazole, prochloraz, Prothioco- Nazole, tebuconazole, triadimefon, triadimenol, triflumizole , Triticonazole, • dicarboximides such as iprodione, myclozolin, procymidone, vinclozolin,
- Dithiocarbamates such as Ferbam, Nabam, Maneb, Mancozeb, Metam, Metiram, Propinerb, Polycarbamat, Thiram, Ziram, Zineb,
- Heterocyclic compounds such as anilazine, benomyl, boscalid, carbendazim, carboxin, oxycarboxin, cyazofamid, Dazomet, dithianon, famoxadone, fenamidon, fenarimol, fuberidazole, flutolanil, furametpyr, isoprothiolan, mepronquin, prozolifene, proba Pyroquilon, Quinoxyfen, Silthiofam, Thiabendazol, Thifluzamid, Thiophanat-methyl, Tiadinil, Tricyclazol, Triforine, Copper fungicides such as Bordeaux broth, copper acetate, copper oxychloride, basic copper sulfate,
- Nitrophenyl derivatives such as binapacryl, dinocap, dinobutone, nitrophthal-isopropyl,
- fungicides such as acibenzolar-S-methyl, benthiavalicarb, carpropamide, chlorothalonil, cyflufenamid, cymoxanil, Dazomet, diclomezin, diclocymet, diethofencarb, edifenphos, ethaboxam, fenhexamide, fentin acetate, fenoxanil, fosetylamino, fefosetone, ferimosone, ferimzone Iprovalicarb, hexachlorobenzene, metrafenone, pencycuron, propamocarb, phthalide, toloclofos-methyl, quintozene, zoxamide
- Sulfenic acid derivatives such as Captafol, Captan, dichlofluanid, Folpet, Tolylfluanid
- Cinnamic acid amides and analogues such as dimethomorph, flumetover or flumorph.
- Preferred mixing partners are metalaxyl din, dodemorph, fenpropimorph, Fenpropi-, guazatine, spiroxamine Nazole, tridemorph, pyrimethanil, Cyrodinyl, bitertanol, Bromoco-, cyproconazole, difenoconazole, Dinitroconazol, epoxiconazole, fenbuconazole, Fluquiconazol, flusilazole, hexaconazole, imazalil, metconazole, myclobutanil , Penconazole, propiconazole, prochloraz, prothioconazole, tebuconazole, triadimefon, triadimenol, triflumizole, triticonazole,
- Azoxystrobin dimoxystrobin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin or trifloxystrobin,
- Particularly preferred blending partners are metalaxyl, fenpropidin, guazatine, spiroxamine, cyproconazole, difenoconazole, fenbuconazole, fluquiconazole, tricolorazolone, proline , Carbendazim, Carboxin, Oxycarboxin, Cyazofamid, Dithianon,, Quinoxyfen, Thiophanat-methyl, Dinocap Nitrophthalisopropyl, Fenpiclonil or Fludioxonil, Benthiavalicarb, Carpropamid, Fenhexamid, Fenoxanil, Fluazinam Iprovalicarb, Metrafenon, Zrafonox.
- Very particularly preferred mixing partners are fenpropimorph, cyproconazole, difenoconazole, epoxiconazole, fenbuconazole, fluquiconazole, flusilazole, hexaconazole, metconazole, myclobutanil propiconazole, prochloraz, prothioconazole, tebuconazole, triticonazole
- Boscalid Boscalid, dithianon,, quinoxyfen, thiophanate-methyl, dinocap fenpiclonil or fludioxonil,
- Benthiavalicarb Carpropamid, Fenhexamid, Fenoxanil, Fluazinam Iprovalicarb, Metrafenon, Zoxamid, Dimethomorph, Azoxystrobin, Dimoxystrobin, Fluoxastrobin, Kresoximmethyl, Metominostrobin, Orysastrobin, Picoxystrobin or Trifloxystrobin.
- the active substance formulations according to the invention can contain different amounts and types of additives, for example solvents.
- solvents can be used to produce the statistical radical polymers and the active substance formulations according to the invention.
- the active substance formulations according to the invention can also be in the form of a liquid solution.
- Suitable solvents are alcohols, e.g. Methanol, ethanol, isopropanol, dipolar aprotic solvents such as e.g. DMF, DMSO or NMP, aromatic, aliphatic, halogenated or unhalogenated hydrocarbons, e.g. Hexane, chlorobenzene, toluene or benzene.
- the solvents can also be largely removed.
- the invention also relates to active substance formulations in dried, solid, i.e. largely solvent-free form.
- the solid active ingredient formulations can be in different macroscopic forms. Spray-dried powder, regrind, granules or film may be mentioned as examples of macroscopic shapes.
- the statistically free radical copolymers contained in the active ingredient formulation according to the invention are suitable for dispersing the active ingredient (s) contained in the active ingredient formulation according to the invention in aqueous systems in the form of nanoparticulate dispersions.
- Such nanoparticulate dispersions comprise at least one continuous phase, which in the present invention is an aqueous system, and at least one dispersed phase.
- the nanoparticulate dispersions can contain further additives.
- the present invention therefore also relates to aqueous dispersions containing the active substance formulations according to the invention, an aqueous system and, if appropriate, further additives.
- Such additives are thickening agents, anti-foaming agents, bactericides and antifreezes.
- An aqueous system is understood to mean pure water or water containing a buffer system or salts or other additives such as, for example, water-miscible solvents or mixtures thereof.
- the pH of the aqueous system is generally in the range from 2 to 13, preferably from 3 to 12, particularly preferably from 4 to 10.
- the invention also relates to processes for the production of aqueous dispersions containing the active substance formulations according to the invention and optionally further additives, characterized in that the active substance formulations according to the invention are brought into contact with an aqueous system and dispersed in the customary manner.
- An important property of the dispersions according to the invention is the average particle size of the dispersed particles, determined by quasi-elastic light scattering, which according to the invention is less than 1 micrometer, preferably less than 500 nanometers, particularly preferably less than 100 nanometers.
- Particle size is understood to mean the particle diameter determined by means of quasi-elastic light scattering.
- the method of quasi-elastic light scattering by means of fiber optics is known from the prior art, for example from H. Auweter, D. Hörn, J. Colloid Interf. Be. 105 (1985) 399, D. Lie, D. Horn, Colloid Polym. Be. 269 (1991) 704 or H. Wiese, D. Hörn, J. Chem. Phys. 94 (1991) 6429.
- Anionic and nonionic surfactants are used as dispersants.
- Anionic surfactants are alkyl aryl sulfonates, phenyl sulfonates, alkyl sulfates, alkyl sulfates, alkyl ether sulfates, alkyl aryl ether sulfates, alkyl polyglycol ether phosphates, polyaryl phenyl ether phosphates, alkyl sulfosuccinates, olefin sulfonates, paraffin sulfonates, petroleum fatty sulfonates, sulfonate acids, petroleum sulfonates with formaldehyde or with formaldehyde and phenol and optionally urea as well as condensation products from phenolsulfonic acid, formaldehyde and urea, lignin sulfite waste liquor and lignin sulfonates, including their alkali, alkaline earth, ammonium and amine salts, alkyl
- Nonionic surfactants are, for example, alkylphenol alkoxylates, alcohol alkoxylates, fatty amine alkoxylates, polyoxyethylene glycerol fatty acid esters, castor oil alkoxylates, fatty acid alkoxylates, fatty acid amide alkoxylates, fatty acid polydiethanol amides, lanolin eth oxylates, fatty acid polyglycol esters, isotridecyl acid fatty acid, polyol glycol fatty acids, polyglycol amide, fatty acid polyol glycols, polyglycol amide, fatty acids Polyethylene glycol polypropylene glycol block copolymers, poly ethylene glycol alkyl ether, polypropylene glycol alkyl ether, polyethylene glycol polypropylene glycol ether block copolymers and mixtures thereof.
- Preferred nonionic surfactants are polyethylene glycol polypropylene glycol block copolymers, polyethylene glycol alkyl ethers, polypropylene glycol alkyl ethers, polyethylene glycol polypropylene glycol ether block copolymers and mixtures thereof.
- surfactants are optionally used as additives.
- Suitable surfactants are anionic surfactants and nonionic surfactants, mixtures of the two are preferred.
- viscosity-changing additives are compounds which impart a pseudoplastic flow behavior to the formulation, ie high viscosity at rest and low viscosity in the agitated state.
- Polysaccharides or organic layered minerals such as Xanthan Gum ® (Kelzan ® from Kelco), Rhodopol ® 23 (Rhone Poulenc) or Veegum ® (RT Vanderbilt) or Attaclay ® (Engelhardt) may be mentioned here, for example, where xanthan gum ® is preferably used.
- anti-foaming agents for example, silicone emulsions (such as z.Bsp. Silicone ® SRE, Wacker or Rhodor- sil ® from Rhodia), long-chain alcohols, fatty acids, organofluorine compounds and mixtures thereof.
- Bactericides can be added to the dispersions according to the invention for stabilization.
- Suitable bactericides are, for example Proxel ® from. ICI or Acetide ® RS from. Thor Chemie and Kathon ® MK from Rohm & Haas.
- Suitable antifreeze agents are e.g. Ethylene glycol, propylene glycol or glycerin.
- the dispersions according to the invention can contain 1-5% by weight of buffer, based on the total amount of the formulation for pH regulation, the amount and type of buffer used depending on the chemical properties of the active ingredient or ingredients.
- buffers are alkali salts of weak inorganic or organic acids such as e.g. Phosphoric acid, boric acid, acetic acid, propionic acid, citric acid, fumaric acid, tartaric acid, oxalic acid and succinic acid.
- the invention furthermore relates to processes for the preparation of the active compound formulations according to the invention, characterized in that the at least one active compound and the at least one random radical copolymer are separated from one another in the same or different, preferably miscible, organic compounds. nical solvents and mix the solutions thus obtained and optionally add additives or prepare a common solution by introducing the at least one active ingredient dissolved in an organic solvent and adding and dissolving the at least one random radical copolymer and optionally further additives and then the solvent or solvents are largely removed in the usual way.
- this solution is preferably used for mixing with the active substance or the active substance solution.
- a first step separate solutions of the at least one randomly radical copolymer and the at least one active ingredient are mixed with one another in the same or in different solvents and, optionally, further additives are added.
- a second step the solvent (s) is / are largely removed in the usual way by suitable processes.
- the invention furthermore relates to processes for the preparation of the active ingredient formulation according to the invention, characterized in that the at least one random radical copolymer (component b) is brought into aqueous solution, the at least one active ingredient (component a) in one or more organic solvents, the or the are miscible with water, dissolve, mix the solutions of components a and b with one another, optionally add further additives and, by introducing shear forces, the active substance formulation is obtained in dispersed form and then the solvents are largely removed in the customary manner.
- miscible with water means that the organic solvents can be mixed with water to at least 10% by weight, preferably 15% by weight, particularly preferably 20% by weight, without phase separation.
- this aqueous solution is preferably used for mixing with the active ingredient solution.
- the statistically free radical copolymer (s) and optionally further additives are dissolved in an aqueous system, provided that such an aqueous solution is not already obtained directly from the step of polymer synthesis. Furthermore, the active ingredient or the active ingredients are dissolved in a water-miscible solvent, optionally with the addition of further additives. The two solutions are then mixed together.
- An energy input such as the application of shear forces by high-frequency and high-amplitude shaking or high-frequency stirring, turbinating or by using a mixing chamber is advantageous for obtaining fine particles when mixing the aqueous and organic phase.
- Mixing can be done in a continuous or discontinuous manner. Continuous mixing is preferred.
- the dispersion obtained in this way can be freed from the solvents in a conventional manner as described above.
- Suitable solvents for carrying out the processes for the preparation of the active compound formulation according to the invention are CrC 6 alkyl alcohols such as methanol, ethanol, propanol, isopropanol, 1-butanol, 2-butanol, tert-butanol, esters, ketones such as acetone, methyl ethyl ketone, methyl isopropyl ketone, methyl isobutyl ketone and acetals , Ethers, cyclic ethers such as tetrahydrofuran, aliphatic carboxylic acids such as formic acid, acetic acid, propionic acid, N-substituted or N, N-disubstituted carboxylic acid amides such as acetamide, carboxylic acid esters such as ethyl acetate and lactones such as butyrolactone, dimethylformamide (DMF) and dimethylpropionamide , aliphatic and aromatic chlorinated hydro
- Preferred solvents are methanol, ethanol, isopropanol, dimethylformamide, N-methylpyrrolidone, methylene chloride, chloroform, 1, 2-dichloroethane, chlorobenzene, acetone, methyl ethyl ketone, methyl isopropyl ketone, methyl isobutyl ketone, tetrahydrofuran and mixtures of the solvents mentioned.
- Particularly preferred solvents are methanol, ethanol, isopropanol, dimethylformamide and tetrahydrofuran.
- Suitable solids contents of the solutions are in the concentration range from 0.5 to 30 percent by weight (% by weight), preferably between 1 and 20% by weight.
- the active substance formulations according to the invention are after removal of the or
- the active substance formulations can contain additives.
- oils of various origins mineral oils, coal tar oils, animal and vegetable oils
- aliphatic and aromatic hydrocarbons such as alkylated
- Naphthalenes alcohols such as methanol, ethanol, butanol, cyclohexanol, ketones such as cyclohexanone, polar solvents and amines such as N-methylpyrrolidone.
- Preferred additives are stabilizers and plasticizers.
- Suitable stabilizers can be low molecular weight components such as, for example, mono- and diglycerides, esters of monogylcerides, alkyl glucosides, lecithin, fatty acid derivatives of urea and urethanes.
- Suitable plasticizers are sucrose, glucose, lactose, fructose, sorbitol, mannitol or glycerin.
- the invention further relates to active substance formulations comprising pyraclostrobin, the mean particle diameter determined by quasi-elastic light scattering being less than 1 micrometer, preferably less than 300 nanometers, particularly preferably less than 100 nanometers.
- Particle sizes of nanoparticulate dispersions of active substance formulations with different polymers and different polymer-active substance ratios determined by means of quasi-elastic light scattering. Measurements were taken after 2 and after 24 hours.
- AMPS 2-acrylamido-2-methyl-1-propanesulfonic acid
- PEA phenoxyethyl acrylate n-BA n-butyl acrylate
- the weight fractions of the monomers used are indicated, for example, by the number sequence 50/17/33, so that AMPS / PEA / n-BA 50/17/33 can be read as a polymer which is built up from the monomers 2-acrylamido-2- Methyl 1-propanesulfonic acid, phenoxyethyl acrylate and n-butyl acrylate in a weight ratio of 50 to 17 to 33.
- the molecular weights of the polymers were determined using size exclusion chromatography. Polymethyl methacrylate calibration samples served as the calibration system.
- the column “active ingredient formulation” shows the qualitative and quantitative composition of the respective statistical radical copolymer with which the active ingredient is present in the formulation.
- the weight ratio polymer to active ingredient was 2 to 1 for all formulations.
- the “Concentration” column indicates the concentration at which the active ingredient formulation was applied.
- the "Rating" column indicates the remaining fungal infection after the treatment on a scale of 0 to 100, the number 100 meaning full infection.
- the value given is an average of three individual values.
- MA, EA, BA, PEA methyl, ethyl, butyl, phenoxyethyl acrylate Table 3:
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Abstract
Description
Claims
Priority Applications (11)
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BRPI0415902A BRPI0415902B1 (pt) | 2003-10-30 | 2004-10-19 | formulações de composto ativo, processo para a preparação de dispersões aquosas, processos para a preparação de uma formulação de composto ativo e processo para combater fungos nocivos |
AT04790621T ATE505951T1 (de) | 2003-10-30 | 2004-10-19 | Wirkstoffformulierungen enthaltend copolymere mit sulfonsäure und phenoxyethylacrylat |
EA200600703A EA011824B1 (ru) | 2003-10-30 | 2004-10-19 | Композиции активных веществ в форме наночастиц, способ получения водных дисперсий, способ борьбы с паразитирующими грибками |
CN2004800326015A CN1874677B (zh) | 2003-10-30 | 2004-10-19 | 纳米颗粒状活性物质配制剂 |
AU2004289034A AU2004289034A1 (en) | 2003-10-30 | 2004-10-19 | Nanoparticulate active substance formulations |
JP2006537128A JP4694497B2 (ja) | 2003-10-30 | 2004-10-19 | ナノ粒子状活性物質の配合物 |
DE502004012424T DE502004012424D1 (de) | 2003-10-30 | 2004-10-19 | Wirkstoffformulierungen enthaltend copolymere mit sulfonsäure und phenoxyethylacrylat |
CA2543553A CA2543553C (en) | 2003-10-30 | 2004-10-19 | Nanoparticulate active substance formulations |
US10/576,921 US7994227B2 (en) | 2003-10-30 | 2004-10-19 | Nanoparticulate active substance formulations |
EP04790621A EP1681923B1 (de) | 2003-10-30 | 2004-10-19 | wirkstoffformulierungen enthaltend copolymere mit sulfonsäure und phenoxyethylacrylat |
IL174824A IL174824A0 (en) | 2003-10-30 | 2006-04-06 | Nanoparticulate active substance formulations |
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AT (1) | ATE505951T1 (de) |
AU (1) | AU2004289034A1 (de) |
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CA (1) | CA2543553C (de) |
CR (1) | CR8368A (de) |
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- 2004-10-19 AT AT04790621T patent/ATE505951T1/de active
- 2004-10-19 EP EP04790621A patent/EP1681923B1/de not_active Not-in-force
- 2004-10-19 AU AU2004289034A patent/AU2004289034A1/en not_active Abandoned
- 2004-10-19 CA CA2543553A patent/CA2543553C/en not_active Expired - Fee Related
- 2004-10-19 ES ES04790621T patent/ES2364660T3/es active Active
- 2004-10-19 JP JP2006537128A patent/JP4694497B2/ja not_active Expired - Fee Related
- 2004-10-19 BR BRPI0415902A patent/BRPI0415902B1/pt not_active IP Right Cessation
- 2004-10-19 WO PCT/EP2004/011797 patent/WO2005046328A1/de active Application Filing
- 2004-10-19 CN CN2004800326015A patent/CN1874677B/zh not_active Expired - Fee Related
- 2004-10-19 KR KR1020067008231A patent/KR20060097120A/ko not_active Application Discontinuation
- 2004-10-19 US US10/576,921 patent/US7994227B2/en not_active Expired - Fee Related
- 2004-10-19 EA EA200600703A patent/EA011824B1/ru not_active IP Right Cessation
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2006
- 2006-04-06 IL IL174824A patent/IL174824A0/en unknown
- 2006-04-26 CR CR8368A patent/CR8368A/es not_active Application Discontinuation
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US7994227B2 (en) | 2003-10-30 | 2011-08-09 | Basf Aktiengesellschaft | Nanoparticulate active substance formulations |
EA012571B1 (ru) * | 2004-04-26 | 2009-10-30 | Басф Акциенгезельшафт | Водная фунгицидная композиция, способ её получения и ее применение для борьбы с вредоносными микроорганизмами |
US8741968B2 (en) | 2004-04-26 | 2014-06-03 | Basf Aktiengesellschaft | Aqueous fungicidal composition and use thereof for combating harmful microorganisms |
WO2005102044A1 (de) * | 2004-04-26 | 2005-11-03 | Basf Aktiengesellschaft | Wässrige, fungizide zusammensetzung und deren verwendung zur bekämpfung von schädlichen mikroorganismen |
WO2006094978A3 (de) * | 2005-03-10 | 2007-07-12 | Basf Ag | Verfahren zur herstellung von pestizide enthaltenden wässrigen polymerdispersionen und ihre verwendung |
WO2006094978A2 (de) * | 2005-03-10 | 2006-09-14 | Basf Aktiengesellschaft | Verfahren zur herstellung von pestizide enthaltenden wässrigen polymerdispersionen und ihre verwendung |
US8906399B2 (en) | 2005-04-18 | 2014-12-09 | Basf Aktiengesellschaft | Preparation containing at least one type of fungicidal conazole |
WO2006111327A3 (de) * | 2005-04-18 | 2007-06-28 | Basf Ag | Zubereitung, enthaltend wenigstens ein conazolfungizid, ein weiteres fungizig und ein stabilisierendes c0p0lymer |
US7927617B2 (en) | 2005-04-18 | 2011-04-19 | Basf Aktiengesellschaft | Preparation comprising at least one conazole fungicide |
EA015876B1 (ru) * | 2005-04-18 | 2011-12-30 | Басф Се | Препарат, включающий по меньшей мере один фунгицидный коназол, способ получения препарата (варианты), его применение для борьбы с фитопатогенными грибами, применение сополимера для получения препарата активных соединений и для стабилизирования водной дисперсии смеси активных соединений |
US20090239749A1 (en) * | 2006-07-13 | 2009-09-24 | David John Duncalf | Biocidal compositions |
JP2009542760A (ja) * | 2006-07-13 | 2009-12-03 | ユニリーバー・ナームローゼ・ベンノートシヤープ | ナノ分散体に関する改良 |
JP2010202665A (ja) * | 2006-07-13 | 2010-09-16 | Unilever Nv | 殺生物性組成物に関連する改良 |
EP2059124B1 (de) | 2006-08-03 | 2016-06-15 | Lamberti SpA | Polymeres tensid zur herstellung pestizider agrochemischer zusammensetzungen |
US9522970B2 (en) | 2006-10-05 | 2016-12-20 | Basf Se | Comb polymers and use thereof for the production of active or effective ingredient formulations |
US8211469B2 (en) | 2006-11-13 | 2012-07-03 | Basf Se | Use of block copolymers based on vinyllactams and vinyl acetate as solubilizers |
US9480250B2 (en) | 2006-12-01 | 2016-11-01 | Basf Se | Production of solid solutions of pesticides by short-term superheating and rapid drying |
WO2008065051A2 (de) | 2006-12-01 | 2008-06-05 | Basf Se | Herstellung von festen lösungen von pestiziden durch kurzzeitüberhitzung und schnelle trocknung |
US9402391B2 (en) | 2008-03-25 | 2016-08-02 | Dow Agrosciences Llc | Stabilized oil-in-water emulsions including agriculturally active ingredients |
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US8541012B2 (en) | 2008-12-18 | 2013-09-24 | Basf Se | Aqueous dispersion comprising pesticide particles and dissolved saccharide |
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WO2011157725A3 (en) * | 2010-06-16 | 2012-06-07 | Basf Se | Aqueous active ingredient composition |
WO2012069514A1 (en) | 2010-11-25 | 2012-05-31 | Basf Se | Waterless composition comprising pesticide and copolymers with sulfonic acid groups |
WO2012156257A1 (en) | 2011-05-13 | 2012-11-22 | Basf Se | Acrylate-acrylamide-amps terpolymer as dispersant for agrochemical formulations |
US10455830B2 (en) | 2011-08-23 | 2019-10-29 | Vive Crop Protection Inc. | Pyrethroid formulations |
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US11517013B2 (en) | 2017-08-25 | 2022-12-06 | Vive Crop Protection Inc. | Multi-component, soil-applied, pesticidal compositions |
Also Published As
Publication number | Publication date |
---|---|
CN1874677A (zh) | 2006-12-06 |
CR8368A (es) | 2006-10-05 |
CN1874677B (zh) | 2011-04-06 |
DE10351004A1 (de) | 2005-05-25 |
ATE505951T1 (de) | 2011-05-15 |
US7994227B2 (en) | 2011-08-09 |
KR20060097120A (ko) | 2006-09-13 |
EP1681923B1 (de) | 2011-04-20 |
CA2543553A1 (en) | 2005-05-26 |
BRPI0415902B1 (pt) | 2016-11-29 |
US20070122436A1 (en) | 2007-05-31 |
CA2543553C (en) | 2012-04-10 |
JP4694497B2 (ja) | 2011-06-08 |
AU2004289034A1 (en) | 2005-05-26 |
EP1681923A1 (de) | 2006-07-26 |
ES2364660T3 (es) | 2011-09-08 |
EA200600703A1 (ru) | 2006-08-25 |
DE502004012424D1 (de) | 2011-06-01 |
BRPI0415902A (pt) | 2007-01-16 |
IL174824A0 (en) | 2006-08-20 |
JP2007509869A (ja) | 2007-04-19 |
EA011824B1 (ru) | 2009-06-30 |
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