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Method for producing wettable powder through compound of validamycin A and propiconazole

A technology of wettable powder and Jinggangmycin, which is applied in the field of pesticides, can solve the problems of poor product quality and achieve the effects of convenient operation, high suspension rate and reasonable process

Inactive Publication Date: 2014-07-02
ZHEJIANG QIANJIANG BIOCHEMICAL CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The present invention aims at the problem of poor quality of Jinggangmycin and propiconazole compound wettable powder produced in the prior art, and proposes a high-quality production method of Jinggangmycin and propiconazole compound wettable powder product, which is effective Overcoming the above disadvantages, the products produced have the characteristics of good drug uniformity, high suspension rate, and good drug efficacy. The process is reasonable and suitable for industrialization

Method used

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  • Method for producing wettable powder through compound of validamycin A and propiconazole

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] Weigh 22.4 kg of the original drug containing 95% of propiconazole, dissolve it by heating with 50 liters of industrial absolute ethanol; stir and adsorb with 20 kg of white carbon black for half an hour, and then vacuum dry the white carbon black adsorbent for 3 hours. The temperature is controlled at 65℃; the dried material is pulverized initially, and then 8 kg of wetting and dispersing agent DT-801 additives, 5 kg of DT-882-2 additives and 35.9 kg of kaolin are added for mixing for 2 to 3 hours; Air jet pulverization, adding 6.7 kg of Jinggangmycin A original drug with a content of 60%, and mixing for 2 to 3 hours. After multi-point sampling and testing, ①The content of Jinggangmycin A and propiconazole were 4.1% and 20.2%, respectively, and the suspension rate was 90.2%; ②The content of Jinggangmycin A and propiconazole were 4.2% and 20.1%, respectively, and the suspension rate It was 90.1%; ③The content of Jinggangmycin A and propiconazole were 4.0% and 20.2%, resp...

Embodiment 2

[0022] Weigh 33.6 kg of the original drug containing 95% of propiconazole and heat it with 75 liters of industrial absolute ethanol to dissolve it; stir and adsorb with 30 kg of white carbon black for half an hour, and then vacuum dry the white carbon black adsorbent for 3 hours. The temperature is controlled at 65℃; the dried material is pulverized initially, and 12 kg of wetting and dispersing agent DT-801 additives, 7.5 kg of DT-882-2 additives and 53.85 kg of kaolin are added for mixing for 2 to 3 hours; Air jet pulverization, add 10.05 kg of Jinggangmycin A original drug with a content of 60%, and mix for 2 to 3 hours. After multi-point sampling and testing, ①The content of Jinggangmycin A and propiconazole were 4.2% and 20.1%, respectively, and the suspension rate was 90.3%; ②The content of Jinggangmycin A and propiconazole were 4.3% and 20.2%, respectively, and the suspension rate 90.2%; ③The content of Jinggangmycin A and propiconazole were 4.1% and 20.2%, respectively,...

Embodiment 3

[0024] Weigh 40.32 kg of the original drug containing 95% of propiconazole and dissolve it by heating with 90 liters of industrial acetone; stir and adsorb with 36 kg of silica for half an hour, and then vacuum dry the silica adsorbate for 3 hours, with temperature control At 65°C; the dried material is pulverized initially, and then 14.4 kg of wetting and dispersing agent DT-801 additive, 9 kg of DT-882-2 additive and 64.62 kg of kaolin are added for mixing for 2 to 3 hours; then airflow crushing , Add 12.06 kg of Jinggangmycin A original drug with a content of 60%, and mix for 2 to 3 hours. After multi-point sampling and testing, ①The content of Jinggangmycin A and propiconazole were 4.3% and 20.1%, respectively, and the suspension rate was 90.4%; ②The content of Jinggangmycin A and propiconazole were 4.2% and 20.2%, respectively, and the suspension rate It was 90.3%; ③The content of Jinggangmycin A and propiconazole were 4.4% and 20.3%, respectively, and the suspension rate ...

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Abstract

The invention relates to a method for producing wettable powder through the compound of validamycin A and propiconazole. The method comprises following steps of (1) adding 2-5 times volume of absolute ethyl alcohol or acetone into original propiconazole based on the volume of the original propiconazole, and dissolving; (2) adding white carbon black into the propiconazole ethyl alcohol solution or propiconazole acetone solution, fully mixing so as to form pulp; (3) vacuum drying, and smashing so as to obtain propiconazole mother powder; (4) fully mixing with wetting dispersant and kaolin; (5) smashing through airflow; (6) adding original medicine powder containing 60%-70% of validamycin A, and mixing to obtain a mixture; (7) performing multipoint sampling and detecting on the mixture, packaging and putting in storage after all indexes are qualified through detection. The method is reasonable and is convenient to operate, the homogeneity of medicines of the prepared wettable powder product is good, the suspensibility of the wettable powder is high and is greater than or equal to 85%.

Description

Technical field [0001] The invention relates to the field of pesticides, in particular to a production method for preparing a wettable powder with Jinggangmycin A and propiconazole. Background technique [0002] Validamycin, also known as Validamycin, English name: Validamycin, a low-toxicity bactericide, is an antibiotic produced by actinomycetes. It has strong systemic properties and is easily absorbed by bacterial cells and quickly within it. Conduct, interfere with and inhibit the growth and development of bacterial cells. It is mainly used for rice sheath blight, but also for the prevention and control of rice smut, corn spot and vegetable, cotton, beans and other crop diseases. [0003] Propiconazole, the English common name: propiconazole, is a systemic triazole fungicide with protective and therapeutic effects. It can be absorbed by roots, stems, and leaves, and can be quickly transmitted upwards in the plant body. Prevent and control diseases caused by ascomycetes, basid...

Claims

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Application Information

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IPC IPC(8): A01N25/14A01N43/653A01P3/00A01N43/16
Inventor 陆建卫姚萍华陆春锋王银泉祝金山
Owner ZHEJIANG QIANJIANG BIOCHEMICAL CO LTD
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