Product description:
Common name: Deltamethrin
Trade name: Sadethrin
Chemical name: A-cyanophenoxybenzyl (1R, 3R)-3-(2, 2-dibromoethenyl)-2, 2-dimethyl cyclopropanecarboxylate
CAS Reg. No.: 52918-63-5
Molecular formula: C22H19Br2NO3
Molecular weight: 422. 9
Physical and chemical properties: Pure product is a white powder; M. P. 98-101Centigrade,
Vapour pressure - at 25 Centigrade, 1. 9996 x 10-9 kPa (1. 5 x 10-8 mmHg).
Solubility - At 20Centigrade, 2 ug/l in water, soluble in most aromatic solvents, acetone, ethanol and dioxane.
Stability: Very stable compound; It does not degrade at 40 Centigrade for two years; 1 it is resistant to air and photo-oxidation
It is odourless and non-corrosive
Toxicology: Acute oral LD50: For rats 128 mg/kg (male), 138 mg/kg
(female), Acute percutaneous LD50 for rats and rabbits > 2940mg/kg. High toxict for fish, fish toxicity LC50(96-h): For bluegill 0. 001 ppm; For rainbow trout 0. 006-0. 008 ppm; For honeybees LD50 0. 079ug/bee, however in normal conditions outdoors it is harmless to honeybees, but fish and bees are not harmed under normal conditions of use. Low toxict
To birds.
Application:
USE ALONE: Deltamethrin is effective against most plant pests except cotton mites and cotton boll weevils. It may be applied to food and field crops, market gardens, orchards and vineyards by air or ground spray equipment, at rates of up to 11g/ha or as recommended by the manufacturer. It may also be sprayed on greenhouse plants, on buildings and other inert surfaces, and on animals. Special formulations for oral or
Dipping applications have also proved effective against cattle ectoparasites.
PUBLIC HEALTH USE - Deltamethrin has had some experimental use against disease vector insects with limited success. Its repellent action may limit its effectiveness in some eradication programmes.
HOUSEHOLD USE - Deltamethrin is primarily an agricultural insecticide and has no recommended household use.
Mode of action: The parent compound is the active toxin; Deltamethrin is a neurotoxin acting primarily on the basal ganglia of the central nervous system. It causes repetitive nerve action through prolongation of sodium
Permeability during the recovery phase of the action potential in neurons.
Unit Price/Payment: | T/T in advance |
Origin: | China |
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