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Nanjing Essence Fine-Chemical Co., Ltd.

Dimethomorph 11.3% + Folpet 60% Wdg, Dimethomorph 11.3% + Folpet 60%, Dimethomorph 11.3% + Folpet 60% Wg manufacturer / supplier in China, offering Dimethomorph 11.3% + Folpet 60% Wdg, Cymoxanil + Metalaxyl (64%+8% Wp), Highly Effective Fosetyl-Aluminum (0.8% Wsg) and so on.

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Supplier Homepage Product Fungicide Dimethomorph 11.3% + Folpet 60% Wdg

Dimethomorph 11.3% + Folpet 60% Wdg

FOB Price: Get Latest Price
Min. Order: 1 kg
Port: Shanghai, China
Production Capacity: 50000 Tons Per Year
Payment Terms: L/C, T/T, D/P

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Basic Info
  • Model NO.: WDG/WG
  • Application: Fungicide
  • Raw Material: Fungicide Mixture
  • Conductivity: Systemic Fungicide
  • Formulation Types: Wdg
  • CAS2: 133-07-3
  • Transport Package: 1g-25kg for Solid Formulations
  • Origin: China
  • Appearance: Granules
  • Usage Mode: Protective Agent
  • Application Fields: Agricultural Fungicide
  • Composition: Organic
  • CAS1: 110488-70-5
  • Trademark: Essence
  • Specification: FAO, WHO
  • HS Code: 3808
Product Description
Dimethomorph 11.3% + Folpet 60% WDG

Dimethomorph NOMENCLATURE
Common name dimethomorph (BSI, E-ISO); diméthomorphe ((m) F-ISO) 
IUPAC name (E,Z)-4-[3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)acryloyl]morpholine
Chemical Abstracts name (E,Z)-4-[3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)-1-oxo-2-propenyl]morpholine  CAS RN [110488-70-5]

Dimethomorph APPLICATIONS
Dimethomorph Biochemistry Proposed inhibitor of phospholipid biosynthesis and cell wall synthesis. Inhibits the formation of the oomycete fungal cell wall.

Dimethomorph Mode of action Local systemic fungicide with good protectant and antisporulant activity. Only the (Z)- isomer is intrinsically active, but, because of rapid interconversion of isomers in the light, it has no advantage over the (E)- isomer in practice.

Dimethomorph Uses Fungicide effective against Oomycetes, especially Peronosporaceae and Phytophthora spp. (but not Pythium spp.) in vines, potatoes, tomatoes and other crops. Used in combination with contact fungicides, and applied at 2.0-2.5 kg formulated product/ha.

Folpet NOMENCLATURE
Common name folpet (BSI, E-ISO, (m) F-ISO, ANSI, JMAF); folpel ((m) France) 
IUPAC name N-(trichloromethylthio)phthalimide; N-(trichloromethanesulfenyl)phthalimide
Chemical Abstracts name 2-[(trichloromethyl)thio]-1H-isoindole-1,3(2H)-dione 
CAS RN [133-07-3] 

Folpet APPLICATIONS
Folpet Biochemistry Non-specific thiol reactant, inhibiting respiration.

Folpet Mode of action Foliar fungicide with protective action.

Folpet Uses Control of downy mildews, powdery mildews, leaf spot diseases, scab, excoriosis, black rot, white rot, Gloeosporium rots, Botrytis, Alternaria, Pythium and Rhizoctonia spp. in pome fruit, stone fruit, soft fruit, citrus fruit, vines, olives, hops, potatoes, lettuce, cucurbits, onions, leeks, celery, tomatoes and ornamentals.

Folpet Phytotoxicity Non-phytotoxic, except to sweet cherries and the D'Anjou variety of pears. Russetting is possible in sensitive apple varieties, if applied early in cropping.

Folpet Compatibility Incompatible with strongly alkaline materials.


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