Fluopicolpkd-containing bactericidal composition
A composition and technology of agricultural fungicides, applied in the directions of fungicides, biocides, biocides, etc., can solve the problems of high use cost and easy generation of drug resistance, achieve reasonable components, overcome and eliminate bacteria resistance, crops. good safety effect
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Embodiment 1
[0040] Example 1, Pyflustrobin and propineb, cymoxanil, dimethomorph, flumorph, chlorothalonil, metalaxyl, fluazinam, fluoxamid, benthiazil complex pairing Indoor Toxicity Test of Cucumber Downy Mildew
[0041] Test object: Cucumber downy mildew fungus (Pseudoperonospora cubensis) was cultured in vivo in our laboratory for a long time.
[0042] Test method: refer to "People's Republic of China Agricultural Industry Standard NY / T 1156.11-2008". Select two potted cucumber seedlings with the same growth at the true leaf stage (remove the growth point), dry them naturally after spraying, inoculate after 24 hours of spraying, take fresh cucumber downy mildew diseased leaves, dip them in distilled water with a brush and wash them. Sporangia on the back of diseased leaves, made into sporangia suspension (2-3×10 5 each / ml), evenly spray inoculation on the cucumber seedlings with an inoculation sprayer (pressure 0.1MPa), the test material after inoculation is moved to the artificial ...
Embodiment 2
[0065] Example 2: Combination of pyrflustrobin with propineb, cymoxanil, dimethomorph, flumorph, chlorothalonil, metalaxyl, fluazinam, fluoxamid, and benthiazil Indoor Toxicity Test of Capsicum Blight
[0066] Test object: Pepper blight pathogen (Phytophthora capsici) was provided by the Institute of Biology, Zhejiang University, and has been identified as having strong pathogenicity.
[0067] Test method: refer to the mycelial growth rate method of "Agricultural Industry Standard NY / T 1156.2-2006 of the People's Republic of China". Cultivate the pathogenic bacteria of Pepper blight with PDA medium. When the colony is just full of the petri dish, use a puncher with a diameter of 5mm to form a bacterial block at the edge of the colony, and use an inoculation needle to move the bacterial block to the pre-prepared toxic PDA for cultivation. Then cultured in a 25°C incubator, and each treatment was repeated 4 times. Depending on the growth of the CK colony, use the cross method ...
Embodiment 1
[0078]Formulation Example 1: 60% Pyflustrobin·Propineb Water Dispersible Granules
[0079] Weigh 20% pyrflustrobin, 40% propine zinc, 3% TERSPERSE 2700, 2% diffusing agent NNO (alkyl naphthalene sulfonate formaldehyde condensate), 3% pull open powder BX (dibutyl naphthalene sulfonic acid sodium), 2% K-12 (sodium lauryl sulfate), 3% diatomaceous earth, 5% glucose, and kaolin to 100%.
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