Lambda-cyhalothrin

COMMON NAME: Lambda-cyhalothrin
PHYSICAL AND CHEMICAL PROPERTIES:

Technical grade: white or light yellow powdery solid.

EC formulation is light yellow transparent liquid. 

Melting point ：49.2℃

Vapor pressure ：200μPa (20℃)

Solubility: pure water:0.005mg/L (pH6.2), buffering water:0.004mg/L (pH5.0), acetone, ethyl acetate, methanol, normal hexane, toluene>500mg/L 

TOXICOLOGY:Oral Acute oral LD50 for male rats 79, female rats 56, mice 20 mg/kg. Acute percutaneous LD50 for rats 632-696 mg/kg. Mild eye irritation; non irritant to skin (rabbits). Not a skin sensitiser (guinea pigs). Inhalation LC50 (4h) 0.06 mg/l air (total particulate).

PESTICIDE REGISTRATION CERTIFICATE:PD20084899

FORMULATION AND SPECIFICATION:
Technical grade: 97% or 95% min technical grade
Formulation: 2.5% EC, 5.0%EC.
PACKING:Iron drums, 1000ml/bottle, 180kg/drum, or on the
Client's requirement.
USES: Control of a wide spectrum of insect pests, e.g. aphids, Colorado beetles, thrips, Lepidoptera larvae, Coleoptera larvae and adults, etc., in cereals, hops, ornamentals, potatoes, vegetables, cotton, and other crops. Provides good control of insect-borne plant viruses. Also used for control of insecticide pests in public health.

PRECAUTION:
1. Do not use in mixture with other alkali pesticides.
2.If swallowed, get medical attention. Do not induce vomiting. If inhaled, remove victim to fresh air, get medical attention. If on skin, wash with plenty of soap and water. If in eyes, flush with plenty of water. Get medical attention if irritation occurs and persists.

CAS NO:91465-08-6;68085-85-8

EC NO:

Molecular Formula:C₂₃H₁₉ClF₃NO₃

Molecular Weight:449.8501

Synonyms:;Cyano-3-phenoxybenzyl(1S+1R)-cis-3-(z-2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethyl cyclopropanecarboxylate;Icon;Karate C50;Lambda ;Ninja 10WP;PP321;a-cyano-3-phenoxybenzyl-3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethyl cyclopropanecarboxylate;A reaction product comprising equal quantities of (S)-a-cyano-3-phenoxybenzyl(Z)-(1R,3R)-3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropanecarboxylate and(R)- a-cyano-3-phenoxybenzyl (Z)-(1S,3S)-3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-di;[1a(S*),3a(Z)]-(±-cyano(3-phenoxyphenyl)methyl3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethylcyclopropanecarboxylate;(S)-a-cyano-3-phenoxybenzyl (Z)-(1R)-cis-3-(2-chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylate and (R)-a-cyano-3-phenoxybenzyl (Z)-(1S)-cis-3-(2-chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylate (1:1);A reaction product comprising equal quantities of (S)-a-cyano-3-phenoxybenzyl(Z)-(1R,3R)-3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropanecarboxylate and(R)-a-cyano-3-phenoxybenzyl (Z)-(1S,3S)-3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dim;(S)- a-cyano-3-phenoxybenzyl (Z)-(1R)-cis-3-(2-chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylate and (R)- a-cyano-3-phenoxybenzyl (Z)-(1S)-cis-3-(2-chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylate (1:1);Bate-cypermethrine;Cypermethrine;cyano(3-phenoxyphenyl)methyl (1R,3R)-3-[(1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate;(R)-cyano(3-phenoxyphenyl)methyl (1S,3S)-3-[(1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate;a-cyano-3-phenoxybenzyl-3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2- dimethylcyclopropanecarboxylate;lambda cyhalothrin;cyano(3-phenoxyphenyl)methyl (1S,3S)-3-[(1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate;(1S,3S)-3-[(1Z)-2-Chloro-3,3,3-trifluoro-1-propenyl]-2,2-dimethylcyclopropanecarboxylicacid(R)-cyano(3-phenoxyphenyl)methylester;cyano(3-phenoxyphenyl)methyl 3-(2-chloro-3,3,3-trifluoroprop-1-en-1-yl)-2,2-dimethylcyclopropanecarboxylate;cyano(3-phenoxyphenyl)methyl 3-[(1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate;(S)-cyano(3-phenoxyphenyl)methyl (1S,3S)-3-[(1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate;Cyhalothrin;Cyhalothri;

Molecular Structure: