Paclobutrazol water dispersible granules/tablets and preparation method thereof
A technology of dispersants and dispersible granules, which is applied in botany equipment and methods, biocides, animal repellents, etc., can solve the problems of low suspending agent content, inconvenient transportation, small powder particles, etc., and achieve simple preparation process, Good storage stability, not easy to produce the effect of phytotoxicity
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Embodiment 15
[0032] The preparation of embodiment 15% paclobutrazol water-dispersible granules
[0033] The selection and ratio of original drug and auxiliary agent are: 95% paclobutrazol original drug 5.3% (5.0%), dispersant is acrylic acid copolymer salt 2.0%, calcium lignosulfonate 5.0%, wetting agent pulls apart powder 4.0% %, the disintegrant is ammonium sulfate 8.0%, the binder is starch 7.0%, and the filler is bentonite to make up 100%.
[0034] Calculate the dosage of each component according to the above ratio, weigh, and mix evenly; the formula material is granulated / compressed after being pulverized by ultra-fine airflow; dried; selected. Product testing is carried out according to the quality control indicators of water-dispersible granules / or tablets, including the content of active ingredients, wettability, dispersibility (disintegration), foamability, pH range, suspension rate and thermal storage stability, etc. The specific method is as follows:
[0035] Use a liquid chro...
Embodiment 1
[0039] The performance indicators of the paclobutrazol water-dispersible granules prepared in Example 1 are: paclobutrazol content 5.0%, wettability qualified (15 seconds), dispersibility (disintegration) qualified (6 times), foaming property qualified (10 milliliters), The water content is 1.5%, the pH value is 6.2, the suspension rate is 86%, the sieve analysis is 99%, the heat storage stability is qualified, and the effective component decomposition rate is 1.1%.
Embodiment 210
[0040] The preparation of embodiment 210% paclobutrazol water-dispersible granules
[0041] The selection and proportioning of the original drug and auxiliary agents are: 95% paclobutrazol original drug 10.6% (10.0%), the dispersant is acrylic acid copolymer salt 6.0%, the wetting agent is sodium lauryl polyoxyethylene ether sulfate 3.0%, The disintegrant is urea 8.0%, the binder is dextrin 3.0%, and the filler is light calcium carbonate to make up 100%. The specific preparation process is the same as in Example 1.
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