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Chemical Insecticide For Termites 64% 60% Fenthion ULV Iermite Insecticide CAS 55-38-9

Categories Termite Treatment Chemicals
Brand Name: MOLOTUS
Model Number: Chlorpyrifos 48% EC
Certification: ISO
Place of Origin: CHINA
MOQ: Negotiable
Price: Negotiable
Payment Terms: L/C, T/T, Western Union
Delivery Time: 20-25 days
Packaging Details: 10L, 5L, 1l, 500ML, 250ML,100ML as client's demand
Active Ingrediet: Fenthion
Formulation: 60% 64% ULV
M.F.: C10H15O3PS2
How to kill: Insecticide with contact, stomach, and respiratory action
Compatibility: Incompatible with insecticides and fungicides which are highly alkaline
Chemical name: O,O-dimethyl O-[3-methyl-4-(methylthio)phenyl] phosphorothioate
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    Chemical Insecticide For Termites 64% 60% Fenthion ULV Iermite Insecticide CAS 55-38-9

    Chemical Insecticide For Termites 64% 60% Fenthion ULV Iermite Insecticide CAS 55-38-9

    Quick Details

    Specification of Fenthion
    Common nameFenthion
    Chemical nameO,O-dimethyl O-[3-methyl-4-(methylthio)phenyl] phosphorothioate
    BiochemistryCholinesterase inhibitor.
    Mode of actionInsecticide with contact, stomach, and respiratory action.
    UsesControl of fruit flies, leafhoppers, leaf miners, leaf-eating larvae, stem borers, cereal bugs and other insect pests, in fruit (including citrus), vines, olives, vegetables, cotton, tea, sugar cane, rice, beet, tobacco, ornamentals, etc. For agricultural uses, application rates vary from 60 to 1200 g/ha, depending on crop, pest, pest stage and application method. Control of insect pests (flies, mosquitoes, cockroaches, fleas, ants, ticks, lice, etc.) in public health situations and animal houses, and control of animal ectoparasites.
    Formulation typesFenthion 64% ULV, 60% ULV, 50% EC
    CompatibilityIncompatible with insecticides and fungicides which are highly alkaline.
    Toxicity classWHO (a.i.) II; EPA (formulation) II

    Reviews FAO/WHO 80, 82 (see part 2 of the Bibliography). Oral Acute oral LD50 for male and female rats c. 250 mg/kg. Skin and eye Acute percutaneous LD50 (24 h) for male rats 586, female rats 800 mg/kg; not irritating to skin and eyes (rabbits). Inhalation LC50 (4 h) for male and female rats c. 0.5 mg/l air (aerosol). NOEL (2 y) for rats <5, mice 0.1 mg/kg diet; (1 y) for dogs 2 mg/kg diet. ADI (JMPR) 0.007 mg/kg b.w. [1995, 1997]. Toxicity class WHO (a.i.) II; EPA (formulation) II EC classification R68| T; R23, R48/25| Xn; R21/22| N; R50, R53

    Birds Acute oral LD50 for bobwhite quail 7.2 mg/kg. Dietary LC50 (5 d) for bobwhite quail 60, mallard ducks 1259 mg/kg. Fish LC50 (96 h) for bluegill sunfish 1.7, rainbow trout 0.83, golden orfe 2.7 mg/l. Daphnia EC50 (48 h) 0.0057 mg/l. Algae ErC50 for Scenedesmus subspicatus 1.79 mg/l. Bees LD50 (contact) 0.16 mg/bee. Worms LC50 for Eisenia foetida 375 mg/kg dry soil.

    EHC 63 (WHO, 1986; a general review of organophosphorus insecticides). Animals In mammals, following oral administration, elimination is mainly in the form of hydrolysis products in the urine. Major metabolites are fenthion sulfoxide, fenthion sulfone and their oxygen analogues. These metabolites are hydrolysed in further degradation, forming the corresponding phenols. Plants In plants, fenthion is oxidised to the sulfoxide and sulfone, both of which possess insecticidal properties, and to the monodesmethyl compound of fenthion sulfoxide. Further degradation occurs to the sulfone phosphate, which undergoes hydrolysis. Soil/Environment Koc 1500 (Ware, Rev. Environ. Contam. Toxicol., 123 (1992)). In sediment/water system with and without plants, DT50 is c. 1.5 d (O'Neill et al., Environ. Toxicol. Chem., 8, 759-768 (1989)). The degradation of fenthion occurs rapidly under aerobic conditions, forming the metabolites fenthion sulfoxide, fenthion sulfone, followed by the analogous phenol compounds.

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