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    • 专利摘要:
    The present invention relates to a process wherein the biologically active compound is a solvent of formula RCH (OR ') 2 , a ketal of formula R 2 C (OR') 2 or an orthoester of formula RC (OR ') 3 , wherein the substituents The present invention relates to a biologically active agent as a solution, an emulsion, a suspension, a suspension, an emulsifiable concentrate and a dispersible granule dissolved in the same). Acetals produced from monoaldehydes and alcohols are represented by formula (I) Acetal used in the present invention includes a structure of formula (a). Also, more complex acetal compounds are described herein. Biologically active compounds in such preparations are active organic compounds, in particular herbicides and emollients, insecticides, fungicides, acaricides, nematicides, pheromones and insect repellents. Included embodiments are oil-in-water (O / W) emulsions, emulsifiable concentrates (EC), water dispersible granules (WG) and suspension emulsions (SE). Bioactive compound / acetal formulations provide environmentally safe treatment as formulated herbicides, emollients, insecticides, fungicides, acaricides, nematicides, pheromones and insect repellents, and exhibit low flammability and biodegradability. Formula I
    公开号:KR20020029119A
    申请号:KR1020027002751
    申请日:2000-08-26
    公开日:2002-04-17
    发明作者:바이넬트프랑크；쉐를프란츠자퍼；체러랄프；두키트모하마드트와허
    申请人:카흐홀즈 트라우델, 귀틀라인 파울；클라리안트 게엠베하；
    IPC主号:
    专利说明:

    Biodegradable solutions of biologically active compounds
    [2] Formulations of herbicidal, fungicidal or pesticidal active substances usually use auxiliaries such as solvents, inert fillers (eg chalk, kaolin or silica), in particular surface active substances. These formulations, when used, may allow the formulation to wet the substrate well and / or to be easily dispersed in water. In the case of water dispersible granules, the adjuvant can disintegrate quickly after introduction into the water.
    [3] Problems exist with processes and applications related to the preparation of formulated bio-active compounds, especially those having relatively low melting points of up to 100 ° C. The prior art proposes various solvents for use with these materials. Properly proposed solvents include high boiling alkylbenzenes and xylenes, 1- or 2-methylnaphthalene, dimethylnaphthalene and other polynuclear aromatic compounds. Other water immiscible solvents proposed include paraffin oils, vegetable oils, cycloaliphatic compounds, alkanols (e.g. cyclohexanol and isooctyl alcohol), ethers, ketones (e.g. cyclohexanone, 4-methylcyclohexanone and iso Poron) and esters such as ethyl benzoate and tri-n-butyl phosphate. Many of these solvents have low flash points and bioaccumulation, which poses a problem of danger and toxicity.
    [4] Surprisingly, one class of organic solvents has been found to be quite effective in dissolving organic bioactive compounds that generally have a high flash point and do not bioaccumulate. The present invention is to provide a solvent for formulated bioactive compounds that are biodegradable, which is not dangerous and does not bioaccumulate.
    [5] Summary of the Invention
    [6] Accordingly, the present invention relates to biologically active preparations as liquids, solid or liquid dispersants, suspensions and emulsions comprising biologically active compounds and water-soluble or fat-soluble acetals. Particular exemplary embodiments include emulsifiable concentrates (EC), water dispersible granules (WG), and suspoemulsion.
    [7] It is a further object of the present invention to provide oil-in-water (O / W) emulsions of acetal and biologically active compounds in the oil phase which are stable colloidal dispersants in water.
    [8] Another object of the present invention is to provide a formulated bioactive compound characterized by low volatility, high flash point and toxicologically safe.
    [1] The present invention relates to biologically active organic compounds, in particular solutions, solid and liquid dispersants and emulsions of herbicides and emollients, insecticides, fungicides, acaricides, nematicides, pheromones and repellents, and more particularly pesticidal active substances.
    [9] Broadly, biologically active substances in liquids, dispersants, emulsions, or solid phase adsorbates, together with the acetals according to the invention, are active organic compounds, in particular herbicides and emollients, insecticides, fungicides, acaricides, nematicides, pheromones and insect repellents. to be.
    [10] The active substance may be supplied in the form of a liquid or solid formulation, which typically contains a bioactive substance content of 1 to 80% by weight, preferably 5 to 60% by weight. Biologically active organic compounds which are mixed with acetals according to the invention preferably comprise herbicides and emollients, insecticides, fungicides, acaricides, nematicides, pheromones and insect repellents, in particular the bioactive materials are glufosinate-ammonium, glycol Lipoates, bialaphos; Active substances of the phenoxy class (eg CMPP, MCPA, 2,4-D), phenoxyphenoxy class (eg diclofomethyl) or heteroaryloxyphenoxy class active substances (eg phenoxaprop Ethyl, phenoxaprop-P-ethyl); Active substances of the urea class (e.g. isoproturon, diuron, linuron, monolinuron and chlortoluron), active substances of the class including sulfonylureas (e.g. amidosulfuron, tribenuron (DPX- L5300), thiamethuron-methyl (DPX-M6316), metsulfuron-methyl (DPX-T6376), primisulfuron-methyl and nicosulfuron); Active substances of the class comprising triazine (eg atrazine or simazine), active substances of the class comprising imidazolinone (eg imazapyr, imazaquin, imazetapyr and imazamethabenz) and di Phenyl ether derivatives (e.g. acifluorophene, fluoroglycopene, lactophene and biphenox), dicotylene herbicides (e.g., oxynyl, bromoxynil, dicamba, diflufenican, fluoxypyr, phenmedy Palm, desmedipharm, bentazone, metamitrone, metrizin, chloridazone, etofumesate or the active substance trituraline); Mitigating agents (e.g. EP-A 86750, EP-A 94349, EP-A 191736, EP-A 346620, EP-A 333131, EP-A 269806, EP-A 159290, DE-A 2546845, PCT / EP-90 / 02020 and PCT / EP-90 / 01966; Fungicidally active substances such as triazoles, including triazoles, ciproconazole, myclobutanyl and diclobutrazole; Active substances of the class comprising dithiocarbamates (eg manebs, genebes and mancozebs), benzimidazoles such as carbendazim, or for example procmidone, ifprodione, vinclozoline Active substances such as thiophanate-methyl, cymoxanyl, polpet, copper oxychloride, sulfur or TPTH.
    [11] Insecticides used herein include, but are not limited to, from avermectin, chloroacetanilide, azole, benzonitrile, phenoxide, imidazolinone, nitroaniline, pyrrole, organophosphorus, sulfonylureas and benzimidazoles. It includes the active substance selected. Active substances are known and described in two publications, referred to herein as "Pesticide Manual (by the British Crop Protection Council) or" Farm Chemicals Handbook 91 "(Meister Publishing Company, Willoughby, Ohio). .
    [12] Particular examples of pesticidal substances used with the acetal solvent according to the present invention include, in particular, compounds having a melting point of less than about 100 ° C., for example posalon, acloniphenoxadione mixtures, acloniphen-linuron, aclo Nifen-biphenox, biphenox, acetate, acloniphene, alachlor, aldicab, amethrin, aminocarb, amitraz, azametifoss, azinfos-ethyl, azinfos-methyl, aziprotrin, benol Lacxyl, benfluralin, bensulfide, benzyl, benzoxmate, benzoylprop-ethyl, bifenthrin, vinopacryl, bromophos, bromo-propylate, bromoxynil esters, burimate, Butiobate, Butocacarsim, Carboxin, Chlorbufam, Chlordimefoam, Chlorfenson, Chlormephos, Chlorobenzylate, Fluorochloridone, Chloropropylate, Chloropoxim, Chloprofam, Chlorpyriphos, Chlorine blood Lipo-methyl, clotocarb, cyanoforce, cycloate, cyclooxydim, cyfluthrin, demethone-S-methyl, desmethrin, dialilifos, diazinone, diclofo, dicopol, die Tatyl, Dimethaclor, Dimethomethrin, Dimethoate, Dinobutone, Dinoceb, Dioxabenzophos, DNOC (2-methyl-4,6-dinitrophenol), EPN (O-ethyl O- (4 -Nitrophenyl) -phenylphosphonothioate), etaconazole, etaflulinin, thiophencarb, etofumesate, pampur, phenamifos, phenytropane, phenbubucarb, phenothiocarb, phenoxapro Fen, phenoxycarb, phenpropatrine, penson, flanuprop, fluorochlorine, fluorodiphene, fluoroglycopene, flurechol, fluoroxyupir, formomothione, furolaxyl, purmecyclox, Haloxope, heptenophos, himexazole, iodofenfos, ioxynyl ester, isoprothiolane, linuron, metallaxyl, memeth Zaklor, metamidose, metidathione, methotforlin, metholcarb, monalid, monocrotophos, monolinuron, myclobutanyl, napropamide, nitrapyrine, nitrofen, nitrothalysopropyl, Oxaventinyl, oxadione, oxyfluorophene, parathion-methyl, fenconazole, pendimethalin, pentanochlor, pentoate, phospholane, phosmet, fiprotanil, petrimicarb, prochloraz, pro Fluralin, promecarb, promethone, propachlor, propamocarb, propanyl, propetafoam, propame, propoxate, propatoate, pyrazophos, pyridate, quinalfoss, quizolopop, Resmetrin, cebumethone, simethrin, tebutan, tefluthrin, temefos, tetramethrin, tetrasul, thiophanox, tolsiophosph-methyl, triadimefon, trichlorphone, tridiphan, Mentions triflumizol, trituralin and xylylcarb can do.
    [13] Other pesticides with melting points below 100 ° C. that can be usefully used in the compositions of the present invention include various esters of phenoxyalkanoic acid groups. These include, for example:
    [14] 2,4-D: (2,4-dichlorophenoxy) acetic acid ester;
    [15] 2,4-DB: 4- (2,4-dichlorophenoxy) butyric acid ester;
    [16] 2,4-DB: 2- (2,4-dichlorophenoxy) propionic ester and its optical isomers;
    [17] MCPA: (4-chloro-2-methylphenoxy) acetic acid ester;
    [18] MCPB: 4- (4-chloro-2-methylphenoxy) butyric acid ester or
    [19] Mecoprop: 2- (4-chloro-2-methylphenoxy) propionic ester and its optical isomers.
    [20] For the formulation of lipophilic pesticidal compounds as aqueous or organic preparations and when high melting acetals are used, especially if the selected acetal solvents have partial solubility in water, cosolvents or diluents can be included with them. In the scope of the present invention, the term “co-solvent” means a solvent that is not acetal, and may be a mixture of other single solvents or some other solvent than acetal, mixed with acetal. Organic cosolvents are usually not required, but if present are used in a weight ratio of solvent (s): acetal from 1:10 to 10: 1, or in any amount to form a liquid formulation of lipophilic insecticide material in proper cooperation with acetal. Used and partitioned into organic and / or aqueous phases.
    [21] Acetals used in the present invention are usually prepared by removing water from aldehyde group containing compounds and hydroxy group containing compounds, in particular aldehydes and alcohols, under acidic conditions. Acetals prepared from monoaldehydes and single mono-alcohols are represented by formula (I)
    [22]
    [23] The R group may be saturated or unsaturated branched or straight chain aliphatic or aromatic. Preferably, R is C 1 -C 20 aliphatic, more preferably C 4 - 12 is the aliphatic group. Acetals can be obtained from the reaction of a stoichiometric amount of one or more alcohols with an aldehyde, or from a reaction of a stoichiometric amount of at least 2: 1, such as 2.5 or even from 3: 1 to 5: 1 moles of alcohol: aldehyde. It can manufacture. Single alcohols and aldehydes can be used, or mixtures of different alcohols and single aldehydes, or mixtures of aldehydes and single alcohols, or mixtures of both different alcohols and different aldehydes can be used. Acetal as used herein may have a total of 3 to 50 carbon atoms, but more practically may have 5 to 30 carbon atoms. Preferred acetals have a boiling point of 100 to 300 ° C. Acetals and raw materials for their preparation are described in US Pat. Nos. 2,796,423, 2,842,499 and 3,563,893, which are incorporated herein by reference.
    [24] The definition of the term "aldehyde" herein includes divalent aldehydes (dialdehydes), in particular aldehydes having 2 to 10 carbon atoms. Dialdehydes such as glyoxal, tartaric acid dialdehyde, succinic acid dialdehyde, maleic acid dialdehyde and fumaric acid dialdehyde are particularly suitable for the preparation of acetals used according to the invention. Acetals derived from glyoxal and alcohols have the following formula in which R 'has the meaning as described above:
    [25]
    [26] Alcohol means a mono- or polyhydroxy compound. Thus, the alcohol may be a monovalent or polyvalent (2-20 -OH group) alkanolamine, alkoxylated (EO and / or PO) alcohol or carboxylated, acylated or etherified mono or polyol, where R 'is Each independently may contain 1 to 24 carbon atoms, preferably 4 to 12 carbon atoms, and may be unsubstituted or substituted by O, N or S containing groups. The alcohol may have R 'groups which are branched or straight chain substituted or unsubstituted saturated or unsaturated cyclic or acyclic and aliphatic or aromatic. Examples of mono, di and trihydric alcohols are methyl-, ethyl-, n-propyl-, n-butyl-, i-butyl-, secondary butyl-, trihydroxy propane, glycerol, trimethylol propane, amyl-, octyl -Ethylhexyl, decyl-, octadecyl-alcohol, but some of a number of mono- or polyols. Examples of cyclic alcohols include tetrahydrofurfuryl alcohol, cyclohexanol, cycloheptanol, cyclooctanol, 2-methylcycloheptanol, 3-butylcyclohexanol and 3-methylcyclohexanol. Examples of ether alcohols are lower (C 1 -C 10 , ie methyl, ethyl, propyl, butyl, pentyl, hexyl, etc.) alkyl ethers of mono, di or triethylene or propylene glycol.
    [27] For example, alkoxy substituted oxygenated aldehydes or nonoxygenated aldehydes can be used.
    [28] Preferred acetals are acetals of formula (1).
    [29]
    [30] In Chemical Formula 1,
    [31] R 1 is (C 1 -C 24 ) alkyl, preferably (C 1 -C 12 ) -alkyl and more preferably (C 4 -C 12 ) -alkyl; (C 1 -C 24 ) -alkenyl, preferably (C 2 -C 12 ) -alkenyl; (C 1 -C 4 ) -alkoxy- (C 2 -C 4 ) alkyl; Phenyl or a group -OR 3 or -OR 4, or R 1 is a group represented by the following Chemical Formula 2,
    [32]
    [33] R 2 is hydrogen, wherein B is a single bond, (C 1 -C 2 ) alkylene or —CH═CH—,
    [34] R 2 is hydrogen or has the same meaning as R 1 ,
    [35] R 3 and R 4 are groups of the formula-(AO) x 0R "where A is -C 2 H 4- , -C 3 H 7 -or -C 4 H 8 -and X is an integer from 0 to 4 R ″ is (C 1 -C 24 ) alkyl, preferably (C 1 -C 4 ) alkyl or (C 2 -C 24 ) alkenyl, preferably (C 2 -C 4 ) alkenyl) Or
    [36] R 3 and R 4 are amino- (C 2 -C 4 ) -alkyl, (C 2 -C 4 ) -dialkylamino- (C 2 -C 4 ) -alkyl, hydroxy- (C 2 -C 6 ) -Alkyl, phenyl, benzyl, (C 1 -C 4 ) -alkylphenyl, (C 1 -C 4 ) -alkoxyphenyl, (C 6 -C 8 ) -cycloalkyl, (C 1 -C 4 ) -alkyl- Or (C 6 -C 8 ) -cycloalkyl or tetrahydrofurfuryl, or R 3 and R 4 together are —CH 2 CH (OH) —, —CH 2 CH 2 —, —CH 2 CH (CH 3 ) — , And Form a group selected from the group consisting of.
    [37] Specific acetal embodiments for use presented are as follows:
    [38] Formula from Butyraldehyde and 1,1,1-trimethylol propane Compound,
    [39] Formula from Butyraldehyde and 1,2,3-Trihydroxy Propane Compound,
    [40] Formula from paraaldehyde and 1,2,3-trihydroxy propane Compound of;
    [41] Formula from paraaldehyde and 1,1,1-trimethylol propane reacted at molar ratio of 0.33: 1 Compound of and
    [42] Formula from isobutyroaldehyde and 1,1,1-trimethylol propane reacted at molar ratio of 1: 1 Of compounds.
    [43] Within the meaning of the acetals of formula RCH (OR ′) 2 , ketals of formula R 2 C (OR ′) 2 , wherein R 2 is as defined above for R and orthoesters of formula RC (OR ′) 3 Wherein these R and R 'groups are as defined above for ketal and orthoesters such as straight or branched alkyl, substituted cycloalkyl and unsubstituted cycloalkyl. Examples of R and R 'groups include methyl, ethyl, n-propyl, n-butyl, i-butyl, secondary butyl, amyl, octyl, decyl or octadecyl and the like. When R is cycloalkyl, it can usually be cyclohexyl, cycloheptyl, cyclooctyl, 2-methylcycloheptyl, 3-butylcyclohexyl or 3-methylcyclohexyl, and the like. R may be inertly substituted, ie it may comprise non-reactive substituents such as alkyl, cycloalkyl, ether or halogen and the like. Typically, the inert substituted R group may include 3-chloropropyl, 2-ethoxyethyl, carboethoxymethyl or 4-methyl cyclohexyl and the like. Preferred R groups may be lower alkyl, ie C 1 -C 10 alkyl groups including, for example, methyl, ethyl, n-propyl, i-propyl, butyl, amyl, hexyl, octyl, decyl and the like. Preferably, R and R 'may be butyl, isobutyl or 2-ethylhexyl for ketal.
    [44] Examples of oxygenated acetals used in the present invention can be prepared by reacting with methoxyacetaldehyde and tetrahydrofurfuryl alcohol or mono lower alkyl ethers of mono, di or triethylene or propylene glycol to form complex acetals. Examples of other complex acetals include methoxyacetaldehyde di (alkoxydiethoxyethyl) acetal, methoxyacetaldehyde di (alkoxyethyl) acetal, methoxyacetaldehyde di (alkoxyethoxyethyl), methoxyacetaldehyde di (alkoxydie Methoxyethyl) acetal. Other complex acetals are formed by the reaction of methoxyacetaldehyde with mono alkyl ethers of mono, di or tripropylene glycol.
    [45] In the formation of the acetals described above from aldehydes, conventional manufacturing methods can be used. Thus, one mole of aldehyde is reacted with at least two moles each and preferably, somewhat stoichiometrically with an excess of the particular alcohol or alcohol mixture. The reaction is carried out at elevated temperature in the presence of a catalyst which may be an acid such as hydrochloric acid or p-toluenesulfonic acid or a catalyst which may be a boron trifluoride-ethyl ether complex known in the art. In general, the reaction temperature may vary from about 190 to about 250 ° F. to form the acetal product at a moderately rapid rate. The reactants may be dissolved in a suitable solvent, such as benzene or other organic solvent, and both solvent and water formed during the reaction process may be trapped and collected by a reflux cooler because they are evaporated from the reaction mixture.
    [46] The ratio of acetal in the bioactive formulation can be up to 90% by weight, but generally 10 to 75% by weight and preferably 20 to 50% by weight and especially 40 to 60% by weight of acetal is contained in the formulated embodiment.
    [47] In addition to the active substances and acetals, the formulations usually use surfactants, wetting agents, antifoams and also optionally additional conventional formulation auxiliaries (eg flocculation aids, stabilizers and fillers). In particular, the formulation may optionally contain 2 to 60% by weight, preferably 5 to 50% by weight of one or more wetting agents. Wetting agents are preferably alkanesulfonates, alkylnaphthalenesulfonates, alkylbenzenesulfonates, alkylpolyglycol ether-sulfonates, alkylsulfosuccinic acid half-esters, fatty acid N-methyltaurides, fatty alcohol ethoxylates, ethylene oxide -Propylene oxide block copolymer or a mixture of such humectants.
    [48] In addition to the active substances, acetals and wetting agents, the formulations may also contain antifoam compounds. Examples of antifoaming agents are described, for example, in H.-F. Fink and G. Koerner in technischen Chemie Ullmann's Encyclopedia of Industrial Chemistry, 4th revised and extended edition, Verlag Chemie, Weinheim, Volume 20, page 411-414, and W. Schonfeldt in "Grenzflachenaktive Alkylenoxid-Addukte [Interface-active Alkylene Oxide Adducts] ", Wissenschaftliche Verlagsgesellschaft MBM, Stuttgart 1973, pages 805-853. Solid antifoams include, for example, aluminum stearate. Liquid defoamers include perfluoroalkyl phosphinic acid-phosphononic acid.
    [49] Examples of formulations of bioactive compounds dissolved in acetal are liquid oil-in-water (O / W) emulsions, liquid water-in-oil emulsions, emulsifiable concentrates (EC), suspension emulsions (SE), and water-dispersible granules (WG). Forms are known in the art.
    [50] In liquid formulations, the biologically active substance and acetal are mixed directly in the presence or absence of a cosolvent. Examples of cosolvents are aromatic or aliphatic compounds such as SOLVESSO 150 or N-methyl pyrrolidone, or methylated oils such as methyl esters of soybean oil, cottonseed oil or rapeseed oil or paraffin oil.
    [51] Emulsifiable concentrates (EC) are defined as solutions of biologically active substances in acetal solvents combined with one or more surfactants. Generally, 20 to 80% by weight of acetal, 0.5 to 20% by weight of bioactive compound and 5 to 15% by weight of surfactant are included in the EC form.
    [52] Suspension emulsions (SE) are defined as dispersants of solid and oil droplets dispersed in an aqueous continuous phase. Biologically active compounds may be suspended as undissolved solids, dissolved in oil phase, dispersed in oil phase, and / or suspended in aqueous phase.
    [53] Water dispersible granules (WG) are defined as biologically active compounds that are dissolved in acetal and adsorbed or absorbed by a solid carrier. Solid carriers known in the art include starch, clay and silica, including mixtures and the like. WG may optionally contain wetting or dispersing agents, all of which are well known in the art. WG is formed by preparing a solution of a biologically active compound in acetal, which is sprayed or mechanically mixed and pelletized or granulated by conventional methods. Generally, water dispersible granules comprise 0.5-50% of the bioactive compound, 10-50% of acetal and 5-30% of the surfactant. Useful surfactants with these are anionic, nonionic, zwitterionic and cationic surfactants.
    [54] Formulated bioactive compounds, in emulsion form, select an emulsification system consisting of anionic, nonionic or cationic surfactants or anionic and nonionic surfactants or mixtures of nonionic and cationic surfactants for acetal mixtures. It is preferable. In addition, two nonionic surfactants may be used, one having a more hydrophilic balance and the other having a more lipophilic or hydrophobic balance. Particularly preferred among hydrophobic surfactants are those having low HLB (hydrophilic-lipophilic-banance) and which can act to prevent or inhibit crystal growth of lipophilic biologically active ingredients. This is best achieved when the hydrophobic surfactant is mixed with the active ingredient-acetal mixture and / or dissolved in the active ingredient-acetal mixture such that the melting point is a liquid or surfactant with a significantly lower melting point. Particularly useful for this use are the hydrophobic ethoxylated nonylphenol surfactants or polyoxyalkylated amines or carboxylic acids or esters described above.
    [55] Thus, among the aforementioned surfactants selected in nonionic emulsion systems, surfactants containing 7 or more alkylene oxide units are selected for hydrophilic formulations, while less than seven for lipophilic surfactants. Surfactants containing alkylene oxide units are selected.
    [56] In addition to O / W, it is advantageous to incorporate anionic surfactants such as sulfonic acids, for example long chain alkylbenzene sulfonates, optionally in the form of amine or ammonium salts. For example, ammonium dodecylbenzenesulfonate is advantageously used. In the emulsion compositions described above, anionic surfactants of from about 0 to 10 g / l, preferably from about 2 to 10 g / l are used.
    [57] The following examples describe embodiments of the invention without limiting the invention thereto. % Or parts are by weight.
    [58] Example 1
    [59] Example 1 Water-Dispersible Granules
    [60] a) Liquid preparation for granulation
    [61] A liquid liquid of the following composition is prepared:
    [62] 96.8% technical grade D, L-phenoxaprop-ethyl was dissolved in di-2-ethylhexanol dimethyl acetal (Hostafluid V-4120) at a weight ratio of 1: 2 (active compound: solvent) to make 95 parts;
    [63] A total of 5 parts of a 50:50 mixture (calcium dodecylbenzene sulfonate and ethylene oxide-propylene oxide block copolymer) of anionic and nonionic emulsifiers are added to make up 100 parts by weight of oil.
    [64] The oil phase is adsorbed onto the mixture of the remaining components:
    [65] 10-30 parts of Na C 14 -C 19 --olefin sulfonate (Hostapur R OS, Clariant);
    [66] Antifoaming agent (perfluorinated alkyl phosphine / phosphonic acid-FLUOWET PL-80, Clariant) from 0.1 to 0.5 parts;
    [67] 3 to 5 parts of a cresol / formaldehyde concentrated product (dispersant S-1494, Clariant) as a dispersant;
    [68] 3 to 5 parts of oleyl methyl tauride wetting agent (Hostapon R T, manufactured by Clariant), and
    [69] 10 to 20 parts powdered fumed silica
    [70] b) preparation of granules
    [71] The components are mixed (optionally with 5-10 parts of water) in a ribbon mixer and granulated using any one of extrusion, pan granulation or high shear mixing.
    [72] The resulting granules are dried at 50-80 ° C. so that the moisture content is less than about 1.5%. In this way, a suitable water dispersible granule is obtained, which is a product that is minimally volatile at processing and has a relatively high flash point and easy application of heat.
    [73] Example 2
    [74] Emulsifiable concentrate
    [75] ingredient:
    [76] Fipronil (15% wt / wt)
    [77] Emulsogen 35 10 (butanol EP-PO block copolymer)
    [78] Phenyl sulfonate (alkylbenzene sulfonate-calcium salt (3% by weight))
    [79] Acetal (Hostafluid 4120) up to 100%
    [80] The components are mixed in a vessel with sufficient heat and stirred to decompose. The solution is filtered and used immediately.
    [81] Example 3
    [82] EW-OIL-IN WATER Emulsion
    [83] A homogeneous oily mixture is obtained by mixing posalon (350 g), isobutyraldehyde-bis-2-ethylhexyl acetal Hostafluid 4120 (250 g) and nonylphenol ethylene oxide polycondensate (1 EO: 50 g) under stirring in a vessel. . In another vessel, water (390 kPa), pre-melted ethylene oxide / propylene oxide condensate (EO: PO 70:30; 40 g), dodecylbenzene sulfonate amine salt (4 g), propylene glycol (20 g) and antifoaming agent (2 g) is mixed while heating to about 40 ° C under stirring. Homogenize the aqueous mixture. The oily mixture is then added to the aqueous mixture in a well stirred vessel and water is added to make 1 l as needed. The mixture is then homogenized by passing through a bead mill (1 mm glass beads) or a conventional homogenizer.
    [84] Exemplary EW formulations (g / l) are as follows:
    [85] Example 4
    [86] ingredientVolume (g) Posalon, 6-chloro-3-diethoxyphosphino-thioylthiomethyl-1,3-benzoxazole-2- (3H) -oneisobutyraldehyde-bis-2-ethylhexyl acetal 1: 1 ethylene oxide / Nonylphenol condensate propylene oxide / ethylene oxide condensate (EO: PO 70:30)3502505040Oil phase Dodecylbenzenesulfonic acid amine salt Propylene glycol antifoaming agent4202
    [87] The following examples are made using the same method.
    [88] Example 5
    [89] ingredientVolume (g) Oxidation, 5-tert-butyl-3- (2,4-dichloro-5-isopropoxyphenyl) -1,3,4-oxadiazole-2 (3H) -one-aclonifene, 2-chloro-6- Nitro-3-phenoxy-benzeneamine isobutyraldehyde-bis-2-ethylhexyl acetal alcohol ethoxylate (GenapolR UD079) propylene oxide / ethylene oxide condensate (EO: PO 70:30)1003003005034Oil phase Dodecylbenzenesulfonic acid amine salt3.4 Residual water to make 0.1 propylene glycol antifoam171.7
    [90] Example 6
    [91] ingredientVolume (g) Metallochloraclonenifen, 2-chloro-6-nitro-3-phenoxy-benzeneamineacetophenoneisobutyraldehyde-bis-2-ethylhexyl acetalpropylene oxide / ethylene oxide condensate (EO: PO 70:30)1432571505047Oil phase Dodecylbenzenesulfonic acid amine salt Propylene glycol antifoaming agent4.7242.4
    [92] Example 7 Suspending Emulsion
    [93] Using the organophosphate active ingredient, the following suspension emulsion (suspended carbaryl) is prepared at g / l under the same conditions as above.
    [94] ingredientVolume (g) Technical ethion, 96%, S, S'-methylenebis- (O, O-diethylphosphorodithioate) isobutyraldehyde-bis-2-ethylhexyl acetalcarbaryl7: 1 ethylene oxide / polyaryl-phenol Sulfate Polycondensate (7 EO)26138015050Oil phase 3 Condensate of Ethylene Oxide / Nonylphenol-Residual Amount of Water to 0.1 l of 2,7 and 10 EO (1: 1: 1)85
    [95] Example 8-Emulsions Containing Biologically Active Substances in Both Oils and Aqueous Phases
    [96] ingredientVolume (g) Bromoxinyl Octanoate Bromoxynyl Heptanoate Isobutyraldehyde-bis-2-ethylhexyl Acetalglyphosate IPA Propylene Glycolbutanol-EO / PO Copolymer (Emulsogen 3510)1001002002253040Oil phase Antifoam (Fluowet PL-80) Suspension (clay) Residual water to make 0.1 liter215 residue
    [97] The general method used for the preparation of emulsions (eg Example 7) in which the active ingredient is contained in both the oil phase and the aqueous phase is as follows:
    [98] a. The homogeneous oil phase is prepared by thoroughly mixing the oil phase active ingredient (s) bromocinyl octanoate, bromocinyl heptanoate and the solvent isobutyraldehyde-bis-2-ethylhexyl acetal. If desired, cosolvents such as “TENNECO” 100, 150 or 200 and optionally hydrophobic surfactants can be used.
    [99] b. A homogeneous aqueous phase is prepared by thoroughly mixing an aqueous phase active ingredient (s) and an adjuvant consisting of clay and all other ingredients including water. These components are preferably added in the above order, but the order is generally convenient and may be in such a way as to maintain aqueous phase homogeneity.
    [100] c. The oil phase is slowly added to a well stirred aqueous phase and, if appropriate, water is added to make 1 l. The addition can also be done in the opposite way.
    [101] The mixture is then homogenized by passing it through a homogeneous mixer. The final oil-in-water emulsion is usually a dispersed oil droplet having an average particle size of about 2 to 8 μm, more preferably 3 to 5 μm, and an overall size distribution in the range of 1 to 15 μm.
    [102] In a similar manner as described above, other oil-in-water emulsions can be prepared using other water soluble active ingredients. Water soluble compounds are as follows:
    [103] Asifluorophene sodium: 5- [2-chloro-4- (trifluoromethyl) phenoxy] -2-nitrobenzoic acid sodium salt;
    [104] Dichlorophene sodium: 5,5'-dichloro-2,2'-dihydroxydiphenylmethane;
    [105] Glyphosinate ammonium: 4- [hydroxy (methyl) phosphinoyl] -DL-homoalanine ammonium salt;
    [106] Imazaquin ammonium: 2- (4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) quinoline-3-carboxylic acid ammonium salt;
    [107] Imazaquin: as acid form in the oil phase;
    [108] Imazapyr IPA: 2- (4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) nicotinic acid isopropylammonium salt;
    [109] Imazapyr: as acid form in the oil phase;
    [110] Metsulfuron: 2- [3- (4-methoxy-6-methyl-1,3,5-triazin-2-yl) ureidosulfonyl benzoic acid, which may optionally be present as a water soluble salt upon pH adjustment with a neutralizer Methyl esters;
    [111] Pendimethalin: N- (1-ethylpropyl) -2,6-dinitro-3,4-xyldine or
    [112] Chlorsulfuron: 1- (2-chlorophenylsulfonyl) -3- (4-methoxy-6-methyl-1,3,5-triazine- which may optionally be present as a water soluble salt upon pH adjustment with a neutralizer 2-yl) urea.
    [113] Biologically active formulations according to the invention, containing acetals, have good storage stability in the alkaline range, and formulations comprising bases, for example ammonium compounds, are preferred. When applied in the field of use, acetals are biodegradable into toxicologically safe components.
    权利要求:
    Claims (21)
    [1" claim-type="Currently amended] A composition comprising a biologically active compound and an acetal solvent selected from the group consisting of solutions, emulsions, suspension emulsions and dispersible granules.
    [2" claim-type="Currently amended] The compound of claim 1, wherein the acetal is of the formula R—CH (OR ′) 2 , wherein R is a saturated or unsaturated side-chain or straight-chain aliphatic or aromatic C 1 -C 20 group, and R ′ is each saturated or unsaturated carbon number 1. To the same or different branched or straight chain aliphatic or aromatic alkyl groups from 25 to 25).
    [3" claim-type="Currently amended] The compound of claim 1 wherein the acetal is of formula Wherein R ′ is as defined in claim 2.
    [4" claim-type="Currently amended] 3. The composition of claim 2, wherein R contains 2 to 10 carbon atoms and R 'each independently contains 4 to 25 carbon atoms.
    [5" claim-type="Currently amended] The composition of claim 1 wherein the acetal is a group of formula (1).
    Formula 1

    In Chemical Formula 1,
    R 1 is (C 1 -C 24 ) -alkyl, preferably (C 1 -C 12 ) -alkyl and more preferably (C 4 -C 12 ) -alkyl; (C 1 -C 24 ) -alkenyl, preferably (C 2 -C 12 ) -alkenyl; (C 1 -C 4 ) -alkoxy- (C 2 -C 4 ) -alkyl; Phenyl; Or a group -OR 3 or -OR 4 , or R 1 is a group of formula (2),
    Formula 2

    R 2 is hydrogen, wherein B is a single bond, (C 1 -C 2 ) alkylene or —CH═CH—,
    R 2 is hydrogen or has the same meaning as R 1 ,
    R 3 and R 4 are groups of the formula-(AO) x 0R "where A is -C 2 H 4- , -C 3 H 7 -or -C 4 H 8 -and X is an integer from 0 to 4 R ″ is (C 1 -C 24 ) -alkyl, preferably (C 1 -C 4 ) -alkyl or (C 2 -C 24 ) -alkenyl, preferably (C 2 -C 4 )- Alkenyl), or
    R 3 and R 4 are amino- (C 2 -C 4 ) -alkyl, (C 2 -C 4 ) -dialkylamino- (C 2 -C 4 ) -alkyl, hydroxy- (C 2 -C 6 ) -Alkyl, phenyl, benzyl, (C 1 -C 4 ) -alkylphenyl, (C 1 -C 4 ) -alkoxyphenyl, (C 6 -C 8 ) -cycloalkyl, (C 1 -C 4 ) -alkyl- Or (C 6 -C 8 ) -cycloalkyl or tetrahydrofurfuryl, or R 3 and R 4 together are —CH 2 CH (OH) —, —CH 2 CH 2 —, —CH 2 CH (CH 3 ) —, And Form a group selected from the group consisting of.
    [6" claim-type="Currently amended] The composition of claim 1 further comprising a cosolvent.
    [7" claim-type="Currently amended] The composition of claim 1 wherein the acetal is formed from aliphatic or aromatic monovalent aldehydes and aliphatic or aromatic monohydric alcohols.
    [8" claim-type="Currently amended] The composition of claim 1 wherein the acetal is a reaction product of components comprising a dialdehyde having 2 to 10 carbon atoms and a monovalent alcohol having 4 to 20 carbon atoms.
    [9" claim-type="Currently amended] 10. The composition of claim 8, wherein the dialdehyde is selected from the group consisting of glyoxal, tartaric dialdehyde, succinic dialdehyde, maleic dialdehyde and fumaric acid dialdehyde.
    [10" claim-type="Currently amended] The composition of claim 1 wherein the biologically active substance is selected from the group consisting of herbicides, emollients, fungicides and pesticides.
    [11" claim-type="Currently amended] The composition of claim 1 in the form of an oil-in-water emulsion containing about 0.5 to about 50 weight percent acetal.
    [12" claim-type="Currently amended] The composition of claim 1 wherein the acetal is a reaction product of monoaldehyde and diol, triol and / or polyol.
    [13" claim-type="Currently amended] The composition of claim 1, wherein the boiling point of acetal is from 100 to 300 ° C.
    [14" claim-type="Currently amended] The composition of claim 1, wherein the dispersible granules further comprise a humectant and optionally a coagulant aid, a stabilizer and a filler.
    [15" claim-type="Currently amended] 15. The method of claim 14, wherein the wetting agent consists of alkanesulfonates, alkylnaphthalenesulfonates, alkylbenzenesulfonates, alkylpolyglycol ether-sulfonates, alkylsulfosuccinic acid half-esters, fatty acid N-methylturides and mixtures thereof. Composition selected from the group.
    [16" claim-type="Currently amended] The composition of claim 14 containing 0.5-50% of the biologically active compound, 10-50% of the acetal and 5-30% of the surfactant.
    [17" claim-type="Currently amended] The composition of claim 16 wherein the surfactant is selected from the group consisting of anionic, nonionic, zwitterionic and cationic surfactants.
    [18" claim-type="Currently amended] The perfluoro- (C 6 -C 18 ) -alkylphosphinic acid and perfluoro- (C 6 -C 18 ) -alkylphosphonic acid, alkali metals thereof, ammonium or C 2 -C 18. And an antifoaming agent selected from the group consisting of -alkylammonium salts, salts thereof with C 10 -C 18 -alkylamineethoxylates or ethylenediamine-ethoxylates and mixtures thereof.
    [19" claim-type="Currently amended] The composition of claim 1 wherein the melting point of the bioactive compound is less than about 100 ° C. 3.
    [20" claim-type="Currently amended] The composition of claim 1 wherein the particle size distribution of the oil droplets as O / W emulsion is from about 1 to about 15 μm.
    [21" claim-type="Currently amended] The composition of claim 1 which is a micro-emulsion.
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    同族专利:
    公开号 | 公开日
    US6342466B1|2002-01-29|
    IL148252D0|2002-09-12|
    CN1372437A|2002-10-02|
    JP2003508461A|2003-03-04|
    BR0013764A|2002-05-07|
    WO2001017345A1|2001-03-15|
    CA2383682A1|2001-03-15|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1999-09-02|Priority to US09/389,151
    1999-09-02|Priority to US09/389,151
    2000-08-26|Application filed by 카흐홀즈 트라우델, 귀틀라인 파울, 클라리안트 게엠베하
    2000-08-26|Priority to PCT/EP2000/008328
    2002-04-17|Publication of KR20020029119A
    优先权:
    申请号 | 申请日 | 专利标题
    US09/389,151|US6342466B1|1999-09-02|1999-09-02|Biodegradable solutions of biologically active compounds|
    US09/389,151|1999-09-02|
    PCT/EP2000/008328|WO2001017345A1|1999-09-02|2000-08-26|Biodegradable solutions of biologically active compounds|
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