CN101233857A - Cyhalothrin aqueous emulsion and low energy emulsification preparation thereof - Google Patents
Cyhalothrin aqueous emulsion and low energy emulsification preparation thereof Download PDFInfo
- Publication number
- CN101233857A CN101233857A CNA2008100466523A CN200810046652A CN101233857A CN 101233857 A CN101233857 A CN 101233857A CN A2008100466523 A CNA2008100466523 A CN A2008100466523A CN 200810046652 A CN200810046652 A CN 200810046652A CN 101233857 A CN101233857 A CN 101233857A
- Authority
- CN
- China
- Prior art keywords
- cyhalothrin
- solvent
- acid ester
- cyano
- chloro
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The invention discloses aqueous emulsion of lambda-cyhalothrin, which at least comprises components with weight percent of 1-10 percent of lambda-cyhalothrin, 1-15 percent of solvent, 1-20 percent of surfactant, 0.1-10 percent of stabilizer and the rest is water. Firstly, the lambda-cyhalothrin is dissolved in the solvent and then added with the surfactant which is then homo-dispersed so as to obtain a homogeneous mixed solution; the obtained homogeneous mixed solution is added with the stabilizer and water and then well stirred to obtain milk-white lambda-cyhalothrin aqueous emulsion. The lambda-cyhalothrin aqueous emulsion prepared by the invention does not contain aromatic organic solvent, which reduces the pollution to the environment effectively. The prepared lambda-cyhalothrin aqueous emulsion has the advantages of small grain diameter of droplet, homodisperse and high stability, etc., thus improving the dispersity of lambda-cyhalothrin and the compounded boosters thereof in the lambda-cyhalothrin aqueous emulsion so as to increase the using ratio of primary agent and auxiliary agents. The preparation method of lambda-cyhalothrin aqueous emulsion is simple and low energy consumption.
Description
Technical field:
The present invention relates to a kind of cyhalothrin water emulsion and preparation method thereof, belong to the pesticide producing field.
Background technology:
Cyhalothrin is a gamma cyhalothrin, its adopted name is lambda-cyhalothrin, is a kind of mixture, contains (S)-alpha-cyano-3-phenoxy benzyl (Z)-(1R of equivalent, 3R)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S, 3S)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2,2-dimethyl cyclopropane carboxylic acid ester; Perhaps (S) of equivalent-alpha-cyano-3-phenoxy benzyl (Z)-(1R)-suitable-3-(2-chloro-3,3, the 3-trifluoro-propenyl)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S)-suitable-3-(2-chloro-3,3, the 3-trifluoro-propenyl)-2,2-dimethyl cyclopropane carboxylic acid ester.Cyhalothrin is the pyrethroid insecticides of phase early 1980s exploitation, have extremely strong stomach toxicity and action of contace poison, be used to prevent and treat lepidoptera pests such as leaf roller, diamond-back moth, homoptera pest such as aphid, leafhopper, weevil, coleopteran pest such as chrysomelid, and domestic animal vermins such as boophilus microplus, east horn fly, poultry lice.
At present existing how tame plant produced cyhalothrin, preparation has missible oil, aqueous emulsion, wetting powder etc.Green water base chemical preparation of agricultural chemicals such as microemulsion and aqueous emulsion are the focus of at present domestic and international preparation research and the inexorable trend of pesticidal preparations development, and still, cream preparation and water base chemical preparation mainly still adopt the aromatic organic solvent preparation.Aromatic organic solvent such as benzene,toluene,xylene and some other condensed ring class aromatic solvent etc. are difficult to biological degradation, very serious and the harm of operator itself is restricted to the pollution of environment, in pesticidal preparations even the use that is under an embargo, the preparation of particularly using the aromatic organic solvent preparation on vegetables, fruit tree is resisted consumingly at some national aromatic organic solvents.Therefore, do not use the exploitation of the water base chemical preparations of harmful organic solvent such as aromatic organic solvent to have extremely important meaning.
Summary of the invention:
The purpose of this invention is to provide a kind of cyhalothrin water emulsion and low-energy emulsification preparation method thereof, do not use aromatic organic solvent and reducing the drug effect that the cyhalothrin water emulsion for preparing on the basis of other consumption of organic solvent can be given full play to cyhalothrin, strengthen its desinsection and render a service, and can effectively reduce environmental pollution.
Realize that the technical scheme that the object of the invention adopted is: a kind of cyhalothrin water emulsion comprises the cyhalothrin of 1-10% at least, the solvent of 1-15%, the surfactant of 1-20%, the stabilizing agent of 0.1-10%, all the other are water, above percentage is weight percentage, wherein solvent is an ethanol, propyl alcohol, butanols, isobutanol, amylalcohol, hexanol, enanthol, octanol, isooctanol, cyclohexanone, pentane, hexane, cyclohexane, heptane, octane, isooctane, benzinum, N-Methyl pyrrolidone, the N-octylpyrrolidone, the two pyrrolidines-2 of two C12 thiazolinyls, 5-diketone ethane, the two pyrrolidines-2 of two C12 thiazolinyls, 5-diketone hexane, No. 70 solvent naphthas, No. 90 solvent naphthas, No. 120 solvent naphthas, No. 180 solvent naphthas, No. 190 solvent naphthas, No. 200 solvent naphthas, the alkyl chain length carbon number is the mixture of a kind of in the alkyl methyl esters of 6-18 or some kinds; Surfactant is a polyoxyethylene polyoxypropylene block copolymer, fatty alcohol-polyoxyethylene ether, rope uncle SOPA, phenethyl phenol polyethenoxy formaldehyde condensation products, castor oil polyoxyethylene ether, the alkyl polyoxyethylene formaldehyde condensation products, neopelex, dodecyl sodium sulfate, lauryl sodium sulfate, lauryl alcohol polyethylene glycol oxide sodium sulphate, sorbitan fatty acid ester, sodium lignin sulfonate, soil temperature 20, soil temperature 60, soil temperature 65, soil temperature 80, soil temperature 85, span 20, span 40, sorbester p18, the mixture of a kind of in sorbester p17 and the alkylphenol polyoxyethylene or some kinds; Stabilizing agent is hydrochloric acid, sulfuric acid, phosphoric acid, acetate, propionic acid, butyric acid, valeric acid, ethylene glycol, 1,2-propane diols, 1, the mixture of a kind of in ammediol, glycerine, polyethylene glycol, urea, sodium salicylate and the sodium taurocholate or some kinds.
Above-mentioned cyhalothrin is a gamma cyhalothrin, (S)-alpha-cyano-3-phenoxy benzyl (Z)-(1R that contains equivalent, 3R)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S, 3S)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2,2-dimethyl cyclopropane carboxylic acid ester; Perhaps (S) of equivalent-alpha-cyano-3-phenoxy benzyl (Z)-(1R)-suitable-3-(2-chloro-3,3, the 3-trifluoro-propenyl)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S)-suitable-3-(2-chloro-3,3, the 3-trifluoro-propenyl)-2,2-dimethyl cyclopropane carboxylic acid ester.
The low-energy emulsification preparation method of described cyhalothrin water emulsion may further comprise the steps:
(1) gets the cyhalothrin of 1-10% by weight percentage, the solvent of 1-15%, the surfactant of 1-20%, the stabilizing agent of 0.1-10%, all the other are water, wherein solvent is an ethanol, propyl alcohol, butanols, isobutanol, amylalcohol, hexanol, enanthol, octanol, isooctanol, cyclohexanone, pentane, hexane, cyclohexane, heptane, octane, isooctane, benzinum, N-Methyl pyrrolidone, the N-octylpyrrolidone, the two pyrrolidines-2 of two C12 thiazolinyls, 5-diketone ethane, the two pyrrolidines-2 of two C12 thiazolinyls, 5-diketone hexane, No. 70 solvent naphthas, No. 90 solvent naphthas, No. 120 solvent naphthas, No. 180 solvent naphthas, No. 190 solvent naphthas, No. 200 solvent naphthas, the alkyl chain length carbon number is the mixture of a kind of in the alkyl methyl esters of 6-18 or some kinds; Surfactant is a polyoxyethylene polyoxypropylene block copolymer, fatty alcohol-polyoxyethylene ether, rope uncle SOPA, phenethyl phenol polyethenoxy formaldehyde condensation products, castor oil polyoxyethylene ether, the alkyl polyoxyethylene formaldehyde condensation products, neopelex, dodecyl sodium sulfate, lauryl sodium sulfate, lauryl alcohol polyethylene glycol oxide sodium sulphate, sorbitan fatty acid ester, sodium lignin sulfonate, soil temperature 20, soil temperature 60, soil temperature 65, soil temperature 80, soil temperature 85, span 20, span 40, sorbester p18, the mixture of a kind of in sorbester p17 and the alkylphenol polyoxyethylene or some kinds; Stabilizing agent is hydrochloric acid, sulfuric acid, phosphoric acid, acetate, propionic acid, butyric acid, valeric acid, ethylene glycol, 1,2-propane diols, 1, the mixture of a kind of in ammediol, glycerine, polyethylene glycol, urea, sodium salicylate and the sodium taurocholate or some kinds.
(2) cyhalothrin is dissolved in the solvent;
(3) surfactant is joined in the above-mentioned solvent that dissolves cyhalothrin, be uniformly dispersed even mixed solution;
(4) join stabilizing agent, water in the even mixed solution and stir, obtain milky cyhalothrin water emulsion at last.
Wherein used cyhalothrin is a gamma cyhalothrin, (S)-alpha-cyano-3-phenoxy benzyl (Z)-(1R that contains equivalent, 3R)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S, 3S)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2,2-dimethyl cyclopropane carboxylic acid ester; (S)-alpha-cyano-3-phenoxy benzyl (Z)-(1R)-suitable-3-(2-chloro-3,3,3-trifluoro-propenyl)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S)-suitable-3-(2-chloro-3,3, the 3-trifluoro-propenyl)-2,2-dimethyl cyclopropane carboxylic acid ester.
Compared with prior art, the present invention has the following advantages:
(1) utilizes aromatic organic solvent to dissolve the former medicine of cyhalothrin in the conventional water-emulsion preparation usually, do not contain aromatic organic solvent in the cyhalothrin water emulsion of the present invention's preparation, effectively reduced environmental pollution.
(2) with conventional preparation aqueous emulsion method in the method for the high energy shear that uses, the present invention has that preparation is simple, low power consumption and other advantages.
(3) being about 1.0 μ m with the aqueous emulsion oil droplet fineness of utilizing the preparation of method such as high energy shear compares, the cyhalothrin water emulsion that makes with the inventive method has size droplet diameter little (about 0.2 μ m), is uniformly dispersed, stable advantages of higher, therefore improve pesticide active ingredient cyhalothrin and the dispersity of composite adjuvant in emulsion thereof, thereby improved the availability of host and assistant agent.
Embodiment:
Embodiment 1
Get (S)-alpha-cyano-3-phenoxy benzyl (Z)-(1R of quality such as containing, 3R)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S, 3S)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2, the former medicine 1kg of the cyhalothrin of 2-dimethyl cyclopropane carboxylic acid ester, place the mixed solvent of 0.5kg isooctanol and 1kg methyl caprylate and 1kg benzinum, add 3.5kg alkyl polyoxyethylene formaldehyde condensation products after the dissolving again, 1kg soil temperature 80 and 0.2kg sldium lauryl sulfate and be uniformly dispersed even mixed solution, add 0.8kg ethylene glycol and 91kg dispersion medium water then in the gained even mixed solution and mix, obtaining milky mass percent at last is 1% cyhalothrin water emulsion.
Embodiment 2
Get (S)-alpha-cyano-3-phenoxy benzyl (Z)-(1R of quality such as containing, 3R)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S, 3S)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2, the former medicine 2.5kg of the cyhalothrin of 2-dimethyl cyclopropane carboxylic acid ester, place the two pyrrolidines-2 of the two C12 thiazolinyls of 2kg isobutanol and 2.7kg70 solvent naphtha and 0.3kg, in the mixed solvent of 5-diketone hexane, add the 2kg alkylphenol polyoxyethylene after the dissolving again, 3.5kg ethoxylated dodecyl alcohol and 0.5kg neopelex and be uniformly dispersed even mixed solution, in the gained even mixed solution, add 0.5kg1 then, 3 propane diols and 86kg dispersion medium water also mix, and obtaining milky mass percent at last is 2.5% cyhalothrin water emulsion
Embodiment 3
Get (S)-alpha-cyano-3-phenoxy benzyl (Z)-(1R of quality such as containing, 3R)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S, 3S)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2, the former medicine 5kg of the cyhalothrin of 2-dimethyl cyclopropane carboxylic acid ester, place the mixed solvent of 4.5kg n-octyl alcohol and 1.7kgN-octylpyrrolidone, add the 3kg castor oil polyoxyethylene ether after the dissolving again, 2.5kg alkyl polyoxyethylene formaldehyde condensation products and 1.5kg sldium lauryl sulfate and be uniformly dispersed even mixed solution, in the gained even mixed solution, add 0.5kg1 then, ammediol, 0.1kg acetate and 81.2kg dispersion medium water also mix, obtaining milky mass percent at last is 5% cyhalothrin water emulsion.
Embodiment 4
Get and quality (S)-alpha-cyano-3-phenoxy benzyl (Z)-(1R)-suitable-3-(2-chloro-3 such as contain, 3, the 3-trifluoro-propenyl)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S)-suitable-3-(2-chloro-3,3, the 3-trifluoro-propenyl)-2, the former medicine 7.5kg of the cyhalothrin of 2-dimethyl cyclopropane carboxylic acid ester, place the mixed solvent of 4.5kg benzinum and 2kg N-Methyl pyrrolidone and 2kg normal octane, add the 3kg polyoxyethylene polyoxypropylene block copolymer after the dissolving again, 2.5kg soil temperature 20 and 1.5kg lauryl sodium sulfate and be uniformly dispersed even mixed solution, in the gained even mixed solution, add 1kg 1 then, the 2-propane diols, 0.2kg hydrochloric acid and 75.8kg dispersion medium water also mix, obtaining milky mass percent at last is 7.5% cyhalothrin water emulsion.
Embodiment 5
Get and quality (S)-alpha-cyano-3-phenoxy benzyl (Z)-(1R)-suitable-3-(2-chloro-3 such as contain, 3, the 3-trifluoro-propenyl)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S)-suitable-3-(2-chloro-3,3, the 3-trifluoro-propenyl)-2, the former medicine 10kg of the cyhalothrin of 2-dimethyl cyclopropane carboxylic acid ester, place the mixed solvent of 3.5kg methyl caproate and 2.5kgN-methyl pyrrolidone and 4kg isooctane, add 4kg alkyl polyoxyethylene formaldehyde condensation products after the dissolving again, 2.5kg sorbester p17 and 2.5kg sodium lignin sulfonate and be uniformly dispersed even mixed solution, in the gained even mixed solution, add the 1kg glycerine then, 0.3kg phosphoric acid and 69.7kg dispersion medium water also mix, obtaining milky mass percent at last is 10% cyhalothrin water emulsion.
Claims (4)
1. cyhalothrin water emulsion, at least comprise 1～10% cyhalothrin, 1～15% solvent, 1～20% surfactant, 0.1～10% stabilizing agent, all the other are water, above percentage is weight percentage, wherein solvent is an ethanol, propyl alcohol, butanols, isobutanol, amylalcohol, hexanol, enanthol, octanol, isooctanol, cyclohexanone, pentane, hexane, cyclohexane, heptane, octane, isooctane, benzinum, N-Methyl pyrrolidone, the N-octylpyrrolidone, the two pyrrolidines-2 of two C12 thiazolinyls, 5-diketone ethane, the two pyrrolidines-2 of two C12 thiazolinyls, 5-diketone hexane, No. 70 solvent naphthas, No. 90 solvent naphthas, No. 120 solvent naphthas, No. 180 solvent naphthas, No. 190 solvent naphthas, No. 200 solvent naphthas, the alkyl chain length carbon number is the mixture of a kind of in the alkyl methyl esters of 6-18 or some kinds; Surfactant is a polyoxyethylene polyoxypropylene block copolymer, fatty alcohol-polyoxyethylene ether, rope uncle SOPA, phenethyl phenol polyethenoxy formaldehyde condensation products, castor oil polyoxyethylene ether, the alkyl polyoxyethylene formaldehyde condensation products, neopelex, dodecyl sodium sulfate, lauryl sodium sulfate, lauryl alcohol polyethylene glycol oxide sodium sulphate, sorbitan fatty acid ester, sodium lignin sulfonate, soil temperature 20, soil temperature 60, soil temperature 65, soil temperature 80, soil temperature 85, span 20, span 40, sorbester p18, the mixture of a kind of in sorbester p17 and the alkylphenol polyoxyethylene or some kinds; Stabilizing agent is hydrochloric acid, sulfuric acid, phosphoric acid, acetate, propionic acid, butyric acid, valeric acid, ethylene glycol, 1,2-propane diols, 1, the mixture of a kind of in ammediol, glycerine, polyethylene glycol, urea, sodium salicylate and the sodium taurocholate or some kinds.
2. cyhalothrin water emulsion according to claim 1, it is characterized in that: cyhalothrin is a gamma cyhalothrin, contain (S)-alpha-cyano-3-phenoxy benzyl (Z) of equivalent-(1R, 3R)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S, 3S)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2,2-dimethyl cyclopropane carboxylic acid ester; Perhaps (S) of equivalent-alpha-cyano-3-phenoxy benzyl (Z)-(1R)-suitable-3-(2-chloro-3,3, the 3-trifluoro-propenyl)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S)-suitable-3-(2-chloro-3,3, the 3-trifluoro-propenyl)-2,2-dimethyl cyclopropane carboxylic acid ester.
3. the low-energy emulsification preparation method of the described cyhalothrin water emulsion of claim 1 is characterized in that may further comprise the steps:
(1) gets 1～10% cyhalothrin by weight percentage, 1～15% solvent, 1～20% surfactant, 0.1～10% stabilizing agent, all the other are water, wherein solvent is an ethanol, propyl alcohol, butanols, isobutanol, amylalcohol, hexanol, enanthol, octanol, isooctanol, cyclohexanone, pentane, hexane, cyclohexane, heptane, octane, isooctane, benzinum, N-Methyl pyrrolidone, the N-octylpyrrolidone, the two pyrrolidines-2 of two C12 thiazolinyls, 5-diketone ethane, the two pyrrolidines-2 of two C12 thiazolinyls, 5-diketone hexane, No. 70 solvent naphthas, No. 90 solvent naphthas, No. 120 solvent naphthas, No. 180 solvent naphthas, No. 190 solvent naphthas, No. 200 solvent naphthas, the alkyl chain length carbon number is the mixture of a kind of in the alkyl methyl esters of 6-18 or some kinds; Surfactant is a polyoxyethylene polyoxypropylene block copolymer, fatty alcohol-polyoxyethylene ether, rope uncle SOPA, phenethyl phenol polyethenoxy formaldehyde condensation products, castor oil polyoxyethylene ether, the alkyl polyoxyethylene formaldehyde condensation products, neopelex, dodecyl sodium sulfate, lauryl sodium sulfate, lauryl alcohol polyethylene glycol oxide sodium sulphate, sorbitan fatty acid ester, sodium lignin sulfonate, soil temperature 20, soil temperature 60, soil temperature 65, soil temperature 80, soil temperature 85, span 20, span 40, sorbester p18, the mixture of a kind of in sorbester p17 and the alkylphenol polyoxyethylene or some kinds; Stabilizing agent is hydrochloric acid, sulfuric acid, phosphoric acid, acetate, propionic acid, butyric acid, valeric acid, ethylene glycol, 1,2-propane diols, 1, the mixture of a kind of in ammediol, glycerine, polyethylene glycol, urea, sodium salicylate and the sodium taurocholate or some kinds.
(2) cyhalothrin is dissolved in the solvent;
(3) surfactant is joined in the above-mentioned solvent that dissolves cyhalothrin, be uniformly dispersed even mixed solution;
(4) join stabilizing agent, water in the even mixed solution and stir, obtain milky cyhalothrin water emulsion at last.
4. the low-energy emulsification preparation method of cyhalothrin water emulsion according to claim 3 is characterized in that:
Described cyhalothrin is a gamma cyhalothrin, (S)-alpha-cyano-3-phenoxy benzyl (Z)-(1R that contains equivalent, 3R)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S, 3S)-3-(2-chloro-3,3,3-trifluoropropyl-1-alkene)-2,2-dimethyl cyclopropane carboxylic acid ester; (S)-alpha-cyano-3-phenoxy benzyl (Z)-(1R)-suitable-3-(2-chloro-3,3,3-trifluoro-propenyl)-2,2-dimethyl cyclopropane carboxylic acid ester and (R)-alpha-cyano-3-phenoxy benzyl (Z)-(1S)-suitable-3-(2-chloro-3,3, the 3-trifluoro-propenyl)-2,2-dimethyl cyclopropane carboxylic acid ester.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200810046652 CN101233857B (en) | 2008-01-09 | 2008-01-09 | Cyhalothrin aqueous emulsion and low energy emulsification preparation thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200810046652 CN101233857B (en) | 2008-01-09 | 2008-01-09 | Cyhalothrin aqueous emulsion and low energy emulsification preparation thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101233857A true CN101233857A (en) | 2008-08-06 |
| CN101233857B CN101233857B (en) | 2013-03-13 |
Family
ID=39917958
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 200810046652 Expired - Fee Related CN101233857B (en) | 2008-01-09 | 2008-01-09 | Cyhalothrin aqueous emulsion and low energy emulsification preparation thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN101233857B (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101438700B (en) * | 2009-01-08 | 2011-12-14 | 陈琳 | Pyrethroid pesticide aqueous emulsion and method for preparing the same |
| CN103518713A (en) * | 2013-10-12 | 2014-01-22 | 天津市华宇农药有限公司 | Synergist used in 5% avermectin emulsion in water |
| CN105145549A (en) * | 2015-08-12 | 2015-12-16 | 广东中迅农科股份有限公司 | Water emulsion containing styrene-acrylic emulsion and preparation method of water emulsion |
| CN105557688A (en) * | 2016-01-22 | 2016-05-11 | 河北天发化工科技有限公司 | Cyhalothrin emulsion in water and preparing method thereof |
| CN106332876A (en) * | 2016-08-20 | 2017-01-18 | 广东中迅农科股份有限公司 | Pyrethroid-pesticide-containing emulsion in water and preparation method thereof |
| CN106577684A (en) * | 2016-11-04 | 2017-04-26 | 东莞市联洲知识产权运营管理有限公司 | Pesticide nano emulsion in water and preparing method thereof |
| CN112219857A (en) * | 2020-10-28 | 2021-01-15 | 泰兴市新宏阳化工有限公司 | Cyhalothrin aqueous emulsion and low-energy emulsification preparation method thereof |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR056077A1 (en) * | 2005-09-19 | 2007-09-19 | Syngenta Participations Ag | IMPROVED METHODS FOR THE CONTROL OF EARTH PESTS AND / OR DISEASES EMERGED FROM THE EARTH |
-
2008
- 2008-01-09 CN CN 200810046652 patent/CN101233857B/en not_active Expired - Fee Related
Non-Patent Citations (1)
| Title |
|---|
| 任广伟等: "2.5％高效氯氟氰菊酯水乳剂防治烟田烟青虫药效实验", 《农药》 * |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101438700B (en) * | 2009-01-08 | 2011-12-14 | 陈琳 | Pyrethroid pesticide aqueous emulsion and method for preparing the same |
| CN103518713A (en) * | 2013-10-12 | 2014-01-22 | 天津市华宇农药有限公司 | Synergist used in 5% avermectin emulsion in water |
| CN103518713B (en) * | 2013-10-12 | 2015-04-01 | 天津市华宇农药有限公司 | Synergist used in 5% avermectin emulsion in water |
| CN105145549A (en) * | 2015-08-12 | 2015-12-16 | 广东中迅农科股份有限公司 | Water emulsion containing styrene-acrylic emulsion and preparation method of water emulsion |
| CN105557688A (en) * | 2016-01-22 | 2016-05-11 | 河北天发化工科技有限公司 | Cyhalothrin emulsion in water and preparing method thereof |
| CN106332876A (en) * | 2016-08-20 | 2017-01-18 | 广东中迅农科股份有限公司 | Pyrethroid-pesticide-containing emulsion in water and preparation method thereof |
| CN106577684A (en) * | 2016-11-04 | 2017-04-26 | 东莞市联洲知识产权运营管理有限公司 | Pesticide nano emulsion in water and preparing method thereof |
| CN112219857A (en) * | 2020-10-28 | 2021-01-15 | 泰兴市新宏阳化工有限公司 | Cyhalothrin aqueous emulsion and low-energy emulsification preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN101233857B (en) | 2013-03-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101233857B (en) | Cyhalothrin aqueous emulsion and low energy emulsification preparation thereof | |
| CN108552171B (en) | Emulsifiable concentrate formulation | |
| CN101379967B (en) | Methoxycinnamaldehyde disinfectant aqueous emulsion and low energy emulsifying preparation method thereof | |
| CN101112195A (en) | Avermectin micro-emulsion and method for preparing the same | |
| CN101743967B (en) | Mixed insecticide of tea saponin and carbamate insecticide | |
| WO2021093266A1 (en) | Compound insecticidal and acaricidal nano aqueous formulation containing lambda-cyhalothrin and emamectin benzoate, and use thereof | |
| WO2021093271A1 (en) | Beta cypermethrin nano aqueous agent, preparation method therefor and use thereof | |
| CN1836513A (en) | Mixed insecticide composition containing fipronil | |
| CN101743969B (en) | Mixed insecticide of tea saponin and neonicotine insecticide | |
| CN101755752B (en) | Pesticide by mixing tea saponin with pyrrole and pyrazole pesticide | |
| CN102388912A (en) | Fosthiazate aqueous emulsion and preparation method thereof | |
| CN106332876A (en) | Pyrethroid-pesticide-containing emulsion in water and preparation method thereof | |
| CN101530086B (en) | Chlorbenzuron suspending agent and preparation method thereof | |
| CN102726414A (en) | Microemulsion containing fomesafen and quizalofop-p-ethyl, and preparation method thereof | |
| CN101438700A (en) | Pyrethroid pesticide aqueous emulsion and method for preparing the same | |
| CN101755821B (en) | Pesticide by mixing tea saponin with thepyrethroid pesticide | |
| CN108684706A (en) | A kind of graphene pesticide compound and preparation method thereof | |
| CN108464312A (en) | Biochemical compound pesticide preparation for preventing and treating beet armyworm and preparation method thereof | |
| CN101213976A (en) | Self-emulsifying type triazophos emulsion oil and preparation thereof | |
| CN105145619B (en) | A kind of aqueous emulsion of synthetic pyrethroid insecticide and preparation method thereof | |
| CN101743982A (en) | Mixed insecticide of tea saponin and nereistoxin insecticide | |
| CN103997889A (en) | A novel aqueous suspoemulsion | |
| CN101036463B (en) | Method of producing avermectin. sha monasultap | |
| JPH11207706A (en) | Antiseptic insecticide for wood | |
| CN1586199A (en) | High concentration abamectin pest killing micro emulsion |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20130313 Termination date: 20170109 |