Compound composition containing isolongifolenone oxime lactam and Dufulin and preparations thereof
A technology of leaf enone oxime lactam and compound composition, which is applied in the field of pesticides, can solve problems such as unsatisfactory control effects, achieve the effects of reducing the dosage and cost per mu, improving the effect of disease prevention, and significant synergistic effect
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[0038] The invention is illustrated by the following examples, which do not limit the scope of the invention. The original drug of isofenoneoxime lactam 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 isolongifolenone lactam (abbreviated as isolongifolenone lactam in the following table); the active component (B) is diazophos.
[0039] 1. Preparation of wettable powder
[0040] The isolongifolenone oxime lactam, methadone, wetting agent, dispersant, and filler are uniformly mixed, pulverized by a jet mill, and stirred for 30 minutes to obtain the wettable powder of the fungicide of the present invention.
[0041]
[0042]
[0043] 2. Preparation of water dispersible granules
[0044]Mix isolongifolenone oxime lactam, pentadophos, wetting agent, dispersant, disintegrating agent and filler evenly, pulverize through jet mill, stir for 30 minutes,...
Embodiment 2
[0079] Controlling Citrus Canker
[0080] 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".
[0081] 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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