Compound composition containing 2-(p-fluorophenyl)-5-methanesulfonyl-1,3,4-oxadiazole and flutriafol and bactericide
A technology of mesylconazole and compound composition, applied in the field of pesticides, can solve the problems of sustainable development of unfavorable environment, shortened duration of effect, and drug resistance caused by diseases, so as to reduce the dosage and cost per mu, and delay the resistance to antibiotics. The effect of medicinal properties and significant synergistic effects
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[0055] The invention is illustrated by the following examples, which do not limit the scope of the invention. The original drug of mesycloconazole used in the present invention is provided by Guizhou University, and other original drugs and preparations used are commercially available. Wherein the active component (A) is mesyconazole (abbreviated as mesylate in the following tables); the active component (B) is triconazole.
[0056] 1. Preparation of wettable powder
[0057] Mix mesyconazole, triconazole, wetting agent, dispersant, and filler evenly, pulverize through a jet mill, and stir for 30 minutes to obtain the wettable powder of the fungicide of the present invention.
[0058]
[0059] 2. Preparation of water dispersible granules
[0060] Mix mesyconazole, triconazole, wetting agent, dispersant, disintegrating agent, and filler evenly, pulverize through a jet mill, stir for 30 minutes, knead with water, and then add it to a fluidized bed granulation dryer for Gran...
Embodiment 2
[0096] Controlling Citrus Canker
[0097] The test refers to "Pesticide Bioassay Technology" (Edited by Chen Nianchun, published by Beijing Agricultural University Press) and "Pesticide Indoor Bioassay Test Guidelines NY / T1156.2-2006".
[0098] In this test, the inhibition zone method is used. On the aseptic operating table, pour the NA medium onto the NA plate, and after drying, take 0.1ml of the suspension of X. citrus bacteria and spread it evenly on the NA plate with a coating stick. . After drying, punch a hole in the center of the plate with a hole puncher with a diameter of 7 mm, and then take 100 μl of the drug solution into the small hole. 5 replicates for each concentration. The treatment of adding sterile water to the small well was used as the blank control. After treatment, place them in an incubator at 28±0.5°C for sterile cultivation, and take them out after 2 days. The diameter of the inhibition zone (in millimeters) of each treatment was measured by the cr...
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