Germicidal composition prepared from triflumizole and SYP-Z048
A technology of pyridoxazole and flucloxanil, applied in the direction of fungicides, biocides, biocides, etc., can solve the problems of the combination and application of flucloxanil and flucloxanil, etc. Sexuality, reduction of adverse effects, quick effect of drug effect
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Embodiment 1
[0019] Embodiment 1: 11% fluconazole pyridoxazole suspension concentrate
[0020]
[0021] First mix other additives, shear and mix evenly in a shearing machine, then add fluconazole and pyridoxazole, grind in a ball mill for 2-3 hours, so that the particle diameter is less than 5mm, and then it can be prepared 11% Fluconazole Pyridoxazole Suspension Concentrate.
Embodiment 2
[0022] Embodiment 2: 30% flubuconazole·pyridoxazole aqueous emulsion
[0023]
[0024]
[0025] First mix fluconazole, pyridoxazole, mesitylene and sorbitan fatty acid ester to dissolve into a uniform oil phase. Then mix some water and other additives together to dissolve into a uniform water phase. Then add the oil phase to the water phase while stirring at high speed in the reaction kettle, slowly add water until reaching the phase inversion point, then perform high-speed shearing, and add the remaining water, and shear for about 30 minutes to obtain 30% flufenazole · Pyridoxazole emulsion in water.
Embodiment 3
[0026] Embodiment 3: 12% fluconazole · pyridoxazole microemulsion
[0027]
[0028] Dissolve fluclofenazole and pyridoxazole completely with fatty acid methyl ester first, then add other additives, mix evenly, finally add water, stir well, and then you can prepare 12% fluclopyridoxazole microemulsion .
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