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Nanjing Essence Fine-Chemical Co., Ltd.

Azoxystrobin 24% + Cymoxanil 37.5% Wdg, Azoxystrobin 24% + Cymoxanil 37.5%, Azoxystrobin 24% + Cymoxanil 37.5% Wg manufacturer / supplier in China, offering Azoxystrobin 24% + Cymoxanil 37.5% Wdg, Highly Effective 2, 4-D Dimethyl Amine Salt (86.5% SL), Highly Effective Propiconazole + Difenoconazole (25%+25% Ec) and so on.

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Supplier Homepage Product Fungicide Azoxystrobin 24% + Cymoxanil 37.5% Wdg

Azoxystrobin 24% + Cymoxanil 37.5% Wdg

FOB Price: Get Latest Price
Min. Order: 1 kg
Production Capacity: 50000 Tons Per Year
Transport Package: 1g-25kg for Solid Formulations
Payment Terms: L/C, T/T, D/P

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Basic Info
  • Model NO.: WDG
  • Application: Fungicide
  • Raw Material: Methoxyacrylate
  • Conductivity: Systemic Fungicide
  • Formulation Types: Wdg
  • CAS2: 57966-95-7
  • Specification: FAO, WHO
  • HS Code: 3808
  • Appearance: Granules
  • Usage Mode: Protective Agent
  • Application Fields: Agricultural Fungicide
  • Composition: Organic
  • CAS1: 131860-33-8
  • Trademark: Essence
  • Origin: China
Product Description
Azoxystrobin 24% + Cymoxanil 37.5% WDG

Azoxystrobin NOMENCLATURE
Common name azoxystrobine ((f) F-ISO); azoxystrobin (BSI, E-ISO) 
IUPAC name methyl (E)-2-{2-[6-(2-cyanophenoxy)pyrimidin-4-yloxy]phenyl}-3-methoxyacrylate
Chemical Abstracts name methyl (E)-2-[[6-(2-cyanophenoxy)-4-pyrimidinyl]oxy]-α-(methoxymethylene)benzeneacetate 
CAS RN [131860-33-8], formerly [215934-32-0]

Azoxystrobin APPLICATIONS
Azoxystrobin Biochemistry Quinone outside inhibitor. Inhibits mitochondrial respiration by blocking electron transfer between cytochrome b and cytochrome c1, at the ubiquinol oxidising site. Controls pathogenic strains resistant to the 14-demethylase inhibitors, phenylamides, dicarboxamides or benzimidazoles.

Azoxystrobin Mode of action Fungicide with protectant, curative, eradicant, translaminar and systemic properties. Inhibits spore germination and mycelial growth, and also shows antisporulant activity.

Azoxystrobin Uses Controls the following pathogens, at application rates between 100 to 375 g/ha: Erysiphe graminis, Puccinia spp., Leptosphaeria nodorum, Septoria tritici and Pyrenophora teres on temperate cereals; ]and Rhizoctonia solani on rice; Plasmopara viticola and Uncinula necator on vines; Sphaerotheca fuliginea and Pseudoperonospora cubensis on cucurbitaceae; Phytophthora infestans and Alternaria solani on potato and tomato; Mycosphaerella arachidis, Rhizoctonia solani and Sclerotium rolfsii on peanut; Monilinia spp. and Cladosporium carpophilum on peach; Pythium spp. and Rhizoctonia solani on turf; Mycosphaerella spp. on banana; Cladosporium caryigenum on pecan; Elsinoë fawcettii, Colletotrichum spp. and Guignardia citricarpa on citrus; Colletotrichum spp. and Hemileia vastatrix on coffee.

Azoxystrobin Phytotoxicity Good crop safety, except on some varieties of apple (e.g. McIntosh, Cox).

Cymoxanil NOMENCLATURE
Common name cymoxanil (BSI, ANSI, E-ISO, (m) F-ISO) 
IUPAC name 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea
Chemical Abstracts name 2-cyano-N-[(ethylamino)carbonyl]-2-(methoxyimino)acetamide 
CAS RN [57966-95-7] 

Cymoxanil APPLICATIONS
Cymoxanil Mode of action Foliar fungicide with protective and curative action. Has contact and local systemic activity, and also inhibits sporulation.

Cymoxanil Uses Control of Peronosporales, especially Peronospora, Phytophthora, and Plasmopara spp. Normally used in combination with protectant fungicides (to improve residual activity) on a range of crops, including vines, hops, potatoes, tomatoes, cucurbits and lettuce, at 2-3 oz/a.

Cymoxanil Compatibility Incompatible with alkaline materials.
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