WO2019084894A1 - Solvents for agricultural applications and pesticide formulations - Google Patents
Solvents for agricultural applications and pesticide formulations Download PDFInfo
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- WO2019084894A1 WO2019084894A1 PCT/CN2017/109241 CN2017109241W WO2019084894A1 WO 2019084894 A1 WO2019084894 A1 WO 2019084894A1 CN 2017109241 W CN2017109241 W CN 2017109241W WO 2019084894 A1 WO2019084894 A1 WO 2019084894A1
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- ether
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- solvent
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Classifications
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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
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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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
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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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
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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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P15/00—Biocides for specific purposes not provided for in groups A01P1/00 - A01P13/00
Definitions
- the present invention relates to solvents for agricultural applications (e.g., pesticides) and to pesticide formulations.
- a large number of active ingredients are used in the agriculture industry for a variety of purposes including, for example, pesticides.
- a particular active ingredient needs to be used with a solvent that provides excellent dissolution performance.
- a variety of solvents have been regularly utilized in agricultural applications depending on the active ingredient. Identifying a particular solvent to use with an active ingredient can be a time-consuming process.
- the present invention provides solvents for agricultural applications, such as pesticides, that, in some embodiments, have good dissolution properties for a broad range of active ingredients.
- the present invention provides a solvent for agricultural applications that comprises (a) a first component consisting of a polar solvent wherein the polar solvent is a sulfoxide, N-methyl-2-pyrrolidone, ⁇ -butyrolactone, or a combination thereof; (b) a second component consisting of a glycol ether; and (c) a third component consisting of an ether ester of Formula 1:
- R 1 and R 2 are each independently one of an alkyl group having 1 to 4 carbon atoms or an aryl group, wherein R 3 is hydrogen, methyl, or ethyl, and wherein n is 1 to 6.
- the present invention provides a pesticide formulation that comprises a solvent according to any of the embodiments of the present invention disclosed herein and a pesticide.
- the present invention provides a pesticide formulation that comprises (a) 16 to 55 weight percent of dimethyl sulfoxide; (b) 20 to 30 weight percent of glycol ether; (c) 20 to 40 weight percent of ether ester; and (d) 2 to 70 weight percent of pesticide.
- an aqueous composition that includes particles of “a” hydrophobic polymer can be interpreted to mean that the composition includes particles of "one or more′′ hydrophobic polymers.
- the numerical ranges disclosed herein include all values from, and including, the lower and upper value.
- ranges containing explicit values e.g., 1 to 7
- any subrange between any two explicit values is included (e.g., 1 to 2; 2 to 6; 5 to 7; 3 to 7; 5 to 6; etc. ) .
- compositions claimed through use of the term “comprising” may include any additional additive, adjuvant, or compound, whether polymeric or otherwise, unless stated to the contrary.
- the term, “consisting essentially of” excludes from the scope of any succeeding recitation any other component, step, or procedure, excepting those that are not essential to operability.
- the term “consisting of” excludes any component, step, or procedure not specifically delineated or listed.
- solvent and like terms mean a substance that is capable of dissolving another substance (i.e., a solute) to form an essentially uniformly dispersed mixture (i.e., solution) at the molecular or ionic size level.
- a solvent for agricultural applications comprises:
- a first component consisting of a polar solvent wherein the polar solvent is a sulfoxide, N-methyl-2-pyrrolidone, ⁇ -butyrolactone, or a combination thereof;
- R 1 and R 2 are each independently one of an alkyl group having 1 to 4 carbon atoms or an aryl group, wherein R 3 is hydrogen, methyl, or ethyl, and wherein n is 1 to 6. In some embodiments, R 1 and R 2 are ethyl groups, R 3 is hydrogen, and n is 2.
- the first component comprises dimethyl sulfoxide.
- the glycol ether comprises ethylene glycol monobutyl ether, ethylene glycol monopropyl ether, ethylene glycol monohexyl ether, diethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diethylene glycol monobutyl ether, diethylene glycol monohexyl ether, propylene glycol monomethyl ether, dipropylene glycol monomethyl ether, tripropylene glycol monomethyl ether, propylene glycol methyl ether acetate, dipropylene glycol methyl ether acetate, propylene glycol n-propyl ether, dipropylene glycol n-propyl ether, propylene glycol n-butyl ether, dipropylene glycol n-butyl ether, tripropylene glycol n-butyl ether, propylene glycol phenyl ether, propylene glycol diacetate, dipropylene glycol dimethyl ether, or di
- the weight ratio of the polar solvent to the glycol ether to the ether ester (polar solvent: glycol ether: ether ester) is 0.8-2.0: 1.0: 1.0-2.0.
- a pesticide formulation comprises a pesticide and a solvent according to any of the embodiments disclosed herein.
- the polar solvent comprises 16 to 55 weight percent of the formulation
- the glycol ether comprises 20 to 30 weight percent of the formulation
- the ether ester comprises 20 to 40 weight percent of the formulation
- the pesticide comprises 2 to 70 weight percent of the formulation.
- the polar solvent comprises 30 to 50 weight percent of the formulation
- the glycol ether comprises 22 to 28 weight percent of the formulation
- the ether ester comprises 20 to 40 weight percent of the formulation
- the pesticide comprises 10 to 60 weight percent of the formulation.
- the pesticide comprises one or more of tebuconazole, difenoconazole, triazolone, quizalofop-p-ethyl, myclobutanil, and pyraclostrobin.
- a pesticide formulation comprises 16 to 55 weight percent of dimethyl sulfoxide, 20 to 30 weight percent of glycol ether, 20 to 40 weight percent of ether ester, and 2 to 70 weight percent of pesticide.
- Solvents for agricultural applications comprise a first component consisting of a polar solvent wherein the polar solvent is a sulfoxide, N-methyl-2-pyrrolidone, ⁇ -butyrolactone, or a combination thereof; a second component consisting of a glycol ether; and (c) a third component consisting of an ether ester of Formula 1an ether ester of Formula 1:
- R 1 and R 2 are each independently one of an alkyl group having 1 to 4 carbon atoms or an aryl group, wherein R 3 is hydrogen, methyl, or ethyl, and wherein n is 1 to 6. In some embodiments, R 1 and R 2 are ethyl groups, R 3 is hydrogen, and n is 2. In some embodiments, such solvents are used for pesticides.
- the polar solvent of the solvent for agricultural applications can be a sulfoxide, N-methyl-2-pyrrolidone, ⁇ -butyrolactone, or a combination thereof
- the polar solvent component of a solvent for agricultural applications consists of, or is, a sulfoxide, i.e., a compound containing a sulfonyl functional group attached to two carbon atoms. It is a polar functional group.
- Sulfoxides are the oxidized derivatives of sulfides. Representative sulfoxides include, but are not limited to, diethyl sulfoxide, butyl sulfoxide, tetramethylene sulfoxide and dimethyl sulfoxide (DMSO) .
- the first component can consist of one or more sulfoxides. In one embodiment the first component consists of one sulfoxide. In one embodiment the first component consists of two or more sulfoxides. In one embodiment the first component consists of, or is, DMSO (CAS Number 67-68-5) .
- the polar solvent consists of, or is, N-methyl-2-pyrrolidone (CAS Number 872-50-4) .
- the polar solvent consists of, or is, ⁇ -butyrolactone (CAS Number 96-48-0) .
- the polar solvent consists of a combination of a sulfoxide (as described above) and/or N-methyl-2-pyrrolidone and/or ⁇ -butyrolactone.
- solvents of the present invention comprise or consist essentially of 16 to 55 weight percent of the polar solvent.
- Solvents of the present invention in other embodiments, comprise or consist essentially of 30 to 50 weight percent of the polar solvent.
- the polar solvent consists of a sulfoxide. In some such embodiments, the solvent consists of 16 to 55 weight percent sulfoxide. The solvent consists of 30 to 50 weight percent sulfoxide in some embodiments.
- the second component of the solvent for agricultural applications (e.g., pesticides) of the present invention consists of, or is, a glycol ether, i.e., a compound based on an alkyl ether of ethylene glycol or propylene glycol.
- a glycol ether i.e., a compound based on an alkyl ether of ethylene glycol or propylene glycol.
- These solvents typically have a higher boiling point, together with the favorable solvent properties of lower-molecular weight ethers and alcohols.
- glycol ethers include, but are not limited to, ethylene glycol monobutyl ether, ethylene glycol monopropyl ether, ethylene glycol monohexyl ether, diethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diethylene glycol monobutyl ether, diethylene glycol monohexyl ether, propylene glycol monomethyl ether, dipropylene glycol monomethyl ether, tripropylene glycol monomethyl ether, propylene glycol methyl ether acetate, dipropylene glycol methyl ether acetate, propylene glycol n-propyl ether, dipropylene glycol n-propyl ether, propylene glycol n-butyl ether, dipropylene glycol n-butyl ether, tripropylene glycol n-butyl ether, propylene glycol phenyl ether, propylene glycol diacetate, dipropylene glycol dimethyl ether
- glycol ethers examples include those commercially available from The Dow Chemical Company such as Butyl CELLUSOLVE TM ethylene glycol monobutyl ether, Propyl CELLUSOLVE TM ethylene glycol monopropyl ether, Hexyl CELLUSOLVE TM ethylene glycol monohexyl ether, CARBITOL TM diethylene glycol monoethyl ether, Methyl CARBITOL TM diethylene glycol monomethyl ether, Butyl CARBITOL TM diethylene glycol monobutyl ether, Hexyl CARBITOL TM diethylene glycol monohexyl ether, DOWANOL TM PM propylene glycol monomethyl ether, DOWANOL TM DPM dipropylene glycol monomethyl ether, DOWANOL TM TPM tripropylene glycol monomethyl ether, DOWANOL TM PMA propylene glycol methyl ether acetate, DOWANOL TM
- the second component can consist of one or more glycol ethers. In one embodiment the second component consists of one glycol ether. In one embodiment the second component consists of two or more glycol ethers. In one embodiment the second component is an ethylene glycol alkyl ether. In one embodiment the second component is a propylene glycol alkyl ether. In one embodiment the alkyl component of the ethylene or propylene glycol ether is an alkyl group of 2 to 12, or 3 to 10, or 3 to 8, carbon atoms. In one embodiment the second component consists of, or is, diethylene glycol monoethyl ether (CAS Number 111-90-0) .
- solvents of the present invention comprise or consist essentially of 20 to 30 weight percent glycol ether.
- Solvents of the present invention in other embodiments, comprise or consist essentially of 22 to 28 weight percent glycol ether.
- the solvent consists of diethylene glycol monoethyl ether. In some such embodiments, the solvent consists of 20 to 30 weight percent diethylene glycol monoethyl ether. The solvent consists of 22 to 28 weight percent diethylene glycol monoethyl ether in some embodiments.
- the third component of the solvent for agricultural applications (e.g., pesticides) of the present invention consists of, or is, an ether ester of Formula 1:
- R 1 and R 2 are each independently one of an alkyl group having 1 to 4 carbon atoms or an aryl group, wherein R 3 is hydrogen, methyl, or ethyl, and wherein n is 1 to 6. In some embodiments, R 1 and R 2 are ethyl groups, R 3 is hydrogen, and n is 2.
- the ether ester is ethyl-3-ethoxy propionate and is commercially available from The Dow Chemical Company as UCAR TM Ester EEP.
- Solvents for agricultural applications of the present invention can comprise, consist of, or consist essentially of two or more ether esters of Formula 1.
- “Two or more ether esters of Formula 1” means that the solvent comprises at least two distinct ether esters of Formula 1 (e.g., a first ether ester in which R 1 and R 2 methyl and a second ether ester in which R 1 and R 2 are ethyl; or a first ether ester in which n is 2 and a second ether ester in which n is 3 and all other substituents or components of the two ether esters are the same; etc.
- the ether esters can differ from one another in more than one substituent or component, and the solvent can comprise any number of different ether esters of Formula 1.
- solvents of the present invention comprise 20 to 40 percent by weight of ether esters of Formula 1.
- Solvents of the present invention in other embodiments, comprise 25 to 35 weight percent of ether esters of Formula 1.
- the third component of solvents of the present invention consists of 20 to 40 weight percent of ether esters of Formula 1.
- the third component consists of 25 to 35 weight percent of ether esters of Formula 1 in some embodiments.
- Solvents of the present invention are made using known equipment and known techniques.
- the individual components of the solvent are commercially available, liquid at ambient conditions (23°C and atmospheric pressure) , and can simply be mixed with one another using conventional mixing equipment and standard blending protocols.
- the components can be added to one another in any order including simultaneously.
- the solvent is a blend consisting of, or consisting essentially of, a sulfoxide as the first component, a glycol ether as the second component, and the ether ester of Formula 1 (as described above) as the third component.
- the solvent is a blend consisting of, or consisting essentially of, a sulfoxide as the first component, diethylene glycol monoethyl ether as the second component, and the ether ester of Formula 1 (as described above) as the third component.
- the solvent is a blend consisting of, or consisting essentially of, a sulfoxide as the first component, a glycol ether as the second component, and ethyl 3-ethoxypropionate as the third component.
- the solvent is a blend consisting of, or consisting essentially of, a sulfoxide as the first component, diethylene glycol monoethyl ether as the second component, and ethyl 3-ethoxypropionate as the third component.
- the solvent is a blend consisting of, or consisting essentially of, a dimethyl sulfoxide as the first component, a glycol ether as the second component, and the ether ester of Formula 1 (as described above) as the third component.
- the solvent is a blend consisting of, or consisting essentially of, a dimethyl sulfoxide as the first component, diethylene glycol monoethyl ether as the second component, and the ether ester of Formula 1 (as described above) as the third component.
- the solvent is a blend consisting of, or consisting essentially of, a dimethyl sulfoxide as the first component, a glycol ether as the second component, and ethyl 3-ethoxypropionate as the third component.
- the solvent is a blend consisting of, or consisting essentially of, a dimethyl sulfoxide as the first component, diethylene glycol monoethyl ether as the second component, and ethyl 3-ethoxypropionate as the third component.
- the solvent is a blend consisting of, or consisting essentially of, N-methyl-2-pyrrolidone as the first component, a glycol ether as the second component, and the ether ester of Formula 1 (as described above) as the third component.
- the solvent is a blend consisting of, or consisting essentially of, N-methyl-2-pyrrolidone as the first component, diethylene glycol monoethyl ether as the second component, and the ether ester of Formula 1 (as described above) as the third component.
- the solvent is a blend consisting of, or consisting essentially of, N-methyl-2-pyrrolidone as the first component, a glycol ether as the second component, and ethyl 3-ethoxypropionate as the third component.
- the solvent is a blend consisting of, or consisting essentially of, N-methyl-2-pyrrolidone as the first component, diethylene glycol monoethyl ether as the second component, and ethyl 3-ethoxypropionate as the third component.
- the solvent is a blend consisting of, or consisting essentially of, ⁇ -butyrolactone as the first component, a glycol ether as the second component, and the ether ester of Formula 1 (as described above) as the third component.
- the solvent is a blend consisting of, or consisting essentially of, ⁇ -butyrolactone as the first component, diethylene glycol monoethyl ether as the second component, and the ether ester of Formula 1 (as described above) as the third component.
- the solvent is a blend consisting of, or consisting essentially of, ⁇ -butyrolactone as the first component, a glycol ether as the second component, and ethyl 3-ethoxypropionate as the third component.
- the solvent is a blend consisting of, or consisting essentially of, ⁇ -butyrolactone as the first component, diethylene glycol monoethyl ether as the second component, and ethyl 3-ethoxypropionate as the third component.
- the solvent comprises, or consists of, a polar solvent, a glycol ether and an ether ester of Formula 1
- the weight ratio of the polar solvent to the glycol ether to the ether ester is 0.8-2.0: 1.0: 1.0-2.0.
- the solvent comprises, or consists of, dimethyl sulfoxide, glycol ether, and an ether ester of Formula 1
- the weight ratio of dimethyl sulfoxide to the glycol ether to the ether ester is 0.8-2.0: 1.0: 1.0-2.0.
- the solvent comprises, or consists of, dimethyl sulfoxide, diethylene glycol monoethyl ether, and an ether ester of Formula 1
- the weight ratio of dimethyl sulfoxide to the diethylene glycol monoethyl ether to the ether ester is 0.8-2.0: 1.0: 1.0-2.0.
- the solvent comprises, or consists of, dimethyl sulfoxide, diethylene glycol monoethyl ether, and ethyl-3-ethoxy propionate
- the weight ratio of dimethyl sulfoxide to the diethylene glycol monoethyl ether to the ethyl-3-ethoxy propionate is 0.8-2.0: 1.0: 1.0-2.0.
- Solvents according to embodiments of the present invention can be used in a number of agricultural applications.
- solvents of the present invention are useful in forming pesticide formulations of the present invention.
- Pesticide formulations according to the present invention comprise a pesticide and a solvent according to any of the embodiments of solvents for pesticides disclosed herein. These pesticides include, but are not limited to, one or more of tebuconazole, difenoconazole, triazolone, quizalofop-p-ethyl, myclobutanil, and pyraclostrobin.
- a pesticide formulation comprises 10 to 98 weight of a solvent according to any of the solvents for pesticides disclosed herein and 2 to 90 weight percent of the pesticide, each based on the total weight of the formulation. In some embodiments, a pesticide formulation comprises 20 to 80 weight of the solvent and 20 to 80 weight percent of the pesticide, each based on the total weight of the formulation.
- a pesticide formulation consists of 10 to 98 weight of a solvent according to any of the solvents for pesticides disclosed herein and 2 to 90 weight percent of the pesticide, each based on the total weight of the formulation. In some embodiments, a pesticide formulation consists of 20 to 80 weight of the solvent and 20 to 80 weight percent of the pesticide, each based on the total weight of the formulation.
- a pesticide formulation consists essentially of 10 to 98 weight of a solvent according to any of the solvents for pesticides disclosed herein and 2 to 90 weight percent of the pesticide, each based on the total weight of the formulation. In some embodiments, a pesticide formulation consists essentially of 20 to 80 weight of the solvent and 20 to 80 weight percent of the pesticide, each based on the total weight of the formulation.
- a pesticide formulation comprises 16 to 55 weight percent polar solvent, 20 to 30 weight percent of a glycol ether, 20 to 40 weight percent of an ether ester of Formula 1 (as described above) , and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent (wt%) based on the weight of the pesticide formulation, from 16 to 55 weight percent of a polar solvent comprising a sulfoxide, N-methyl-2-pyrrolidone, ⁇ -butyrolactone, or a combination thereof, from 20 to 30 weight percent of a glycol ether, 20 to 40 weight percent of an ether ester of Formula 1 (as described above) , and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent (wt%) based on the weight of the pesticide formulation, from 16 to 55 weight percent of a polar solvent comprising a sulfoxide, N-methyl-2-pyrrolidone, ⁇ -butyrolactone, or a combination thereof, from 20 to 30 weight percent of a glycol ether, 20 to 40 weight percent of an ether ester of Formula 1 (as described above) , and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent (wt%) based on the weight of the pesticide formulation, from 16 to 55 weight percent of a sulfoxide, from 20 to 30 weight percent of a glycol ether, 20 to 40 weight percent of an ether ester of Formula 1 (as described above) , and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent (wt%) based on the weight of the pesticide formulation, from 16 to 55 weight percent of a sulfoxide, from 20 to 30 weight percent of diethylene glycol monoethyl ether, 20 to 40 weight percent of an ether ester of Formula 1 (as described above) , and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent (wt%) based on the weight of the pesticide formulation, from 16 to 55 weight percent of a sulfoxide, from 20 to 30 weight percent of a glycol ether, 20 to 40 weight percent of ethyl 3-ethoxypropionate, and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent (wt%) based on the weight of the pesticide formulation, from 16 to 55 weight percent of a sulfoxide, from 20 to 30 weight percent of diethylene glycol monoethyl ether, 20 to 40 weight percent of ethyl 3-ethoxypropionate, and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent based on the weight of the pesticide formulation, from 16 to 55 weight percent of a polar solvent comprising dimethyl sulfoxide, from 20 to 30 weight percent of a glycol ether, 20 to 40 weight percent of an ether ester of Formula 1 (as described above) , and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent based on the weight of the pesticide formulation, from 16 to 55 weight percent of a polar solvent comprising dimethyl sulfoxide, from 20 to 30 weight percent of diethylene glycol monoethyl ether, 20 to 40 weight percent of an ether ester of Formula 1 (as described above) , and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent based on the weight of the pesticide formulation, from 16 to 55 weight percent of a polar solvent comprising dimethyl sulfoxide, from 20 to 30 weight percent of a glycol ether, 20 to 40 weight percent of ethyl 3-ethoxypropionate, and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent based on the weight of the pesticide formulation, from 16 to 55 weight percent of a polar solvent comprising dimethyl sulfoxide, from 20 to 30 weight percent of diethylene glycol monoethyl ether, 20 to 40 weight percent of ethyl 3-ethoxypropionate, and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent based on the weight of the pesticide formulation, from 16 to 55 weight percent of N-methyl-2-pyrrolidone, from 20 to 30 weight percent of a glycol ether, 20 to 40 weight percent of an ether ester of Formula 1 (as described above) , and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent based on the weight of the pesticide formulation, from 16 to 55 weight percent of N-methyl-2-pyrrolidone, from 20 to 30 weight percent of diethylene glycol monoethyl ether, 20 to 40 weight percent of an ether ester of Formula 1 (as described above) , and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent based on the weight of the pesticide formulation, from 16 to 55 weight percent of N-methyl-2-pyrrolidone, from 20 to 30 weight percent of a glycol ether, 20 to 40 weight percent of ethyl 3-ethoxypropionate, and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent based on the weight of the pesticide formulation, from 16 to 55 weight percent of N-methyl-2-pyrrolidone, from 20 to 30 weight percent of diethylene glycol monoethyl ether, 20 to 40 weight percent of ethyl 3-ethoxypropionate, and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent (wt%) based on the weight of the pesticide formulation, from 16 to 55 weight percent of ⁇ -butyrolactone, from 20 to 30 weight percent of a glycol ether, 20 to 40 weight percent of an ether ester of Formula 1 (as described above) , and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent (wt%) based on the weight of the pesticide formulation, from 16 to 55 weight percent of ⁇ -butyrolactone, from 20 to 30 weight percent of diethylene glycol monoethyl ether, 20 to 40 weight percent of an ether ester of Formula 1 (as described above) , and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent (wt%) based on the weight of the pesticide formulation, from 16 to 55 weight percent of ⁇ -butyrolactone, from 20 to 30 weight percent of a glycol ether, 20 to 40 weight percent of ethyl 3-ethoxypropionate, and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- a pesticide formulation consist of, or consists essentially of, in weight percent (wt%) based on the weight of the pesticide formulation, from 16 to 55 weight percent of ⁇ -butyrolactone, from 20 to 30 weight percent of diethylene glycol monoethyl ether, 20 to 40 weight percent of ethyl 3-ethoxypropionate, and 2 to 70 weight percent of a pesticide, each based on the total weight of the pesticide formulation.
- Optional materials that are not essential to the operability of, but can be included in, the pesticide formulations of this invention include, but are not limited to, antioxidants, colorants, water scavengers, stabilizers, and the like. These materials do not have any material impact on the efficacy of the pesticide formulation. These optional materials are used in known amounts, e.g., 0.10 to 5, or 4, or 3, or 2, or 1, weight percent based on the weight of the solvent, and they are used in known ways.
- Pesticide formulations can be prepared using techniques known to those of skill in the art. For example, the active ingredient (pesticide) can be dissolved in a solvent, and then emulsifiers or other conventional additives can be added.
- the DMSO is from Sinopharm, Co., China.
- the diethylene glycol monoethyl ether is CARBITOL TM from The Dow Chemical Company.
- the ethyl 3-ethoxypropionate is UCAR TM Ester EEP available from The Dow Chemical Company.
- the following solvents are evaluated:
- Each pesticide powder is added by solvent in 2%stepwise increments to the final pesticide concentration.
- Each pesticide reaches a concentration where the pesticide powder is not dissolved by the solvent.
- the concentration just prior to the concentration where the pesticide powder is not dissolved is shown in Table 4.
- Table 4 reflects a solubility that is no more than 2%lower than the actual solubility.
- Inventive Solvent 1 which is a blend of Comparative Solvents A, B, and C exhibits a stronger dissolving power than each of the individual solvents for each of active ingredients that were evaluated. Inventive Solvent 1 thus provides a synergistic effect in terms of dissolving power. In addition, Inventive Solvent 1 effectively dissolves a variety of pesticides as shown in Table 4 and thus acts as a universal solvent for a variety of active ingredients (in this example, pesticides) .
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- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
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Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BR112020008074-8A BR112020008074A2 (pt) | 2017-11-03 | 2017-11-03 | solventes para aplicações agrícolas e formulações de pesticidas |
| US16/638,410 US11547112B2 (en) | 2017-11-03 | 2017-11-03 | Solvents for agricultural applications and pesticide formulations |
| EP17930332.6A EP3703494A4 (en) | 2017-11-03 | 2017-11-03 | SOLVENTS FOR AGRICULTURAL APPLICATIONS AND PESTICIDE FORMULATIONS |
| PCT/CN2017/109241 WO2019084894A1 (en) | 2017-11-03 | 2017-11-03 | Solvents for agricultural applications and pesticide formulations |
| CA3079271A CA3079271C (en) | 2017-11-03 | Solvents for agricultural applications and pesticide formulations | |
| CN201780096147.7A CN111246736B (zh) | 2017-11-03 | 2017-11-03 | 用于农业应用的溶剂和农药调配物 |
| JP2020522844A JP7227238B2 (ja) | 2017-11-03 | 2017-11-03 | 農業用途のための溶媒および農薬製剤 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/CN2017/109241 WO2019084894A1 (en) | 2017-11-03 | 2017-11-03 | Solvents for agricultural applications and pesticide formulations |
Publications (1)
| Publication Number | Publication Date |
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| WO2019084894A1 true WO2019084894A1 (en) | 2019-05-09 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/CN2017/109241 Ceased WO2019084894A1 (en) | 2017-11-03 | 2017-11-03 | Solvents for agricultural applications and pesticide formulations |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US11547112B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP3703494A4 (cg-RX-API-DMAC7.html) |
| JP (1) | JP7227238B2 (cg-RX-API-DMAC7.html) |
| CN (1) | CN111246736B (cg-RX-API-DMAC7.html) |
| BR (1) | BR112020008074A2 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2019084894A1 (cg-RX-API-DMAC7.html) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2026080434A1 (en) * | 2024-10-08 | 2026-04-16 | Eastman Chemical Company | Solvent systems for agrochemical formulations |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998000008A1 (en) | 1996-06-28 | 1998-01-08 | Novartis Ag | Pesticidal compositions |
| WO2005000023A1 (en) | 2003-06-18 | 2005-01-06 | Brook Chandler Murphy | Physical mode of action pesticide |
| CN101971824A (zh) | 2010-11-09 | 2011-02-16 | 上海生农生化制品有限公司 | 一种精噁唑禾草灵与麦草畏的组合物及其应用 |
| CN102283195A (zh) | 2011-09-13 | 2011-12-21 | 广西田园生化股份有限公司 | 一种农药助剂及其制备方法 |
| WO2014060557A2 (en) | 2012-10-19 | 2014-04-24 | Syngenta Participations Ag | Liquid agrochemical compositions comprising a polymeric thickener and an alcohol-containing solvent system, and liquid herbicidal compositions having an alcohol-containing solvent system |
| CN104686542A (zh) | 2015-03-18 | 2015-06-10 | 山西绿海农药科技有限公司 | 含嘧螨酯组合物的超低容量液剂及其制备方法 |
| CN107094777A (zh) | 2017-04-24 | 2017-08-29 | 中国农业科学院植物保护研究所 | 一种防治农业细菌性病害和灭螺的组合物 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8908794D0 (en) * | 1989-04-19 | 1989-06-07 | Janssen Pharmaceutica Nv | Synergistic compositions containing propiconazole and tebuconazole |
| JPH11116994A (ja) * | 1997-10-17 | 1999-04-27 | Kyowa Yuka Kk | アルコキシ酪酸エステルからなる溶剤 |
| CA2436834C (en) | 2000-12-04 | 2010-01-26 | Syngenta Participations Ag | Microemulsifiable agrochemical concentrate |
| EP2409568A1 (en) | 2010-07-19 | 2012-01-25 | Huntsman International Llc | Agrochemical formulation composition |
| WO2012169620A1 (ja) * | 2011-06-10 | 2012-12-13 | 東京応化工業株式会社 | 溶剤現像ネガ型レジスト組成物、レジストパターン形成方法、ブロックコポリマーを含む層のパターン形成方法 |
| PL2548437T3 (pl) | 2011-07-19 | 2017-01-31 | Arysta Lifescience Benelux Sprl | Ulepszony sposób wytwarzania roztworów środków szkodnikobójczych do emulgowania |
| JP6315702B2 (ja) | 2012-02-27 | 2018-04-25 | ハンツマン・コーポレーシヨン・オーストラリア・ピーテイワイ・リミテツド | 農薬乳化性濃厚調剤 |
| CN104145950A (zh) | 2014-07-21 | 2014-11-19 | 浙江省诸暨合力化学对外贸易有限公司 | 一种唑草酮新型乳油及其制备方法 |
| ES2969257T3 (es) * | 2017-11-03 | 2024-05-17 | Dow Global Technologies Llc | Disolventes para aplicaciones agrícolas y formulaciones pesticidas |
-
2017
- 2017-11-03 BR BR112020008074-8A patent/BR112020008074A2/pt not_active Application Discontinuation
- 2017-11-03 JP JP2020522844A patent/JP7227238B2/ja active Active
- 2017-11-03 US US16/638,410 patent/US11547112B2/en active Active
- 2017-11-03 WO PCT/CN2017/109241 patent/WO2019084894A1/en not_active Ceased
- 2017-11-03 EP EP17930332.6A patent/EP3703494A4/en not_active Withdrawn
- 2017-11-03 CN CN201780096147.7A patent/CN111246736B/zh active Active
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998000008A1 (en) | 1996-06-28 | 1998-01-08 | Novartis Ag | Pesticidal compositions |
| WO2005000023A1 (en) | 2003-06-18 | 2005-01-06 | Brook Chandler Murphy | Physical mode of action pesticide |
| CN101971824A (zh) | 2010-11-09 | 2011-02-16 | 上海生农生化制品有限公司 | 一种精噁唑禾草灵与麦草畏的组合物及其应用 |
| CN102283195A (zh) | 2011-09-13 | 2011-12-21 | 广西田园生化股份有限公司 | 一种农药助剂及其制备方法 |
| WO2014060557A2 (en) | 2012-10-19 | 2014-04-24 | Syngenta Participations Ag | Liquid agrochemical compositions comprising a polymeric thickener and an alcohol-containing solvent system, and liquid herbicidal compositions having an alcohol-containing solvent system |
| CN104686542A (zh) | 2015-03-18 | 2015-06-10 | 山西绿海农药科技有限公司 | 含嘧螨酯组合物的超低容量液剂及其制备方法 |
| CN107094777A (zh) | 2017-04-24 | 2017-08-29 | 中国农业科学院植物保护研究所 | 一种防治农业细菌性病害和灭螺的组合物 |
Non-Patent Citations (3)
| Title |
|---|
| KOZUKI, Y.: "A predictive solubility tool for pesticide emulsifiable concentrate formulations", ASTM SPECIAL TECHNICAL PUBLICATION, vol. 6, no. 9, 31 August 2009 (2009-08-31), pages 69 - 81, XP009159561 |
| KOZUKI, Y.: "A predictive solubility tool for pesticide emulsifiable concentrate formulations", ASTM SPECIAL TECHNICAL PUBLICATION, vol. 6, no. 9, 31 August 2009 (2009-08-31), pages 69 - 81, XP009159561, ISSN: 0066-0558 * |
| See also references of EP3703494A4 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2026080434A1 (en) * | 2024-10-08 | 2026-04-16 | Eastman Chemical Company | Solvent systems for agrochemical formulations |
Also Published As
| Publication number | Publication date |
|---|---|
| EP3703494A4 (en) | 2021-06-23 |
| US11547112B2 (en) | 2023-01-10 |
| JP7227238B2 (ja) | 2023-02-21 |
| CA3079271A1 (en) | 2019-05-09 |
| JP2021510366A (ja) | 2021-04-22 |
| US20210392876A1 (en) | 2021-12-23 |
| BR112020008074A2 (pt) | 2020-10-06 |
| CN111246736B (zh) | 2023-06-13 |
| EP3703494A1 (en) | 2020-09-09 |
| CN111246736A (zh) | 2020-06-05 |
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