Product Description

Common name: allethrin; alléthrine; d-allethrin IUPAC name: (RS)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (1R,3R;1R,3S)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate Alt: (RS)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (+)-cis-trans-chrysanthemate Roth: (RS)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (1R)-cis-trans-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate Chemical Abstracts name: 2-methyl-4-oxo-3-(2-propenyl)-2-cyclopenten-1-yl 2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate CAS RN: [584-79-2] (unstated stereochemistry and also used for bioallethrin) EEC no.: 209-542-4 [for (1RS)- isomers] PHYSICAL CHEMISTRY Composition: d-Allethrin is 93% (1R)- isomers and 75% trans isomers; see also bioallethrin. Mol. wt.: 302.4; M.f.: C19H26O3; Form: Tech. is a pale yellow liquid. B.p.: 281.5 °C/760 mmHg. V.p.: 0.16 mPa (21 °C). KOW: logP = 4.96 (room temperature). S.g./density: 1.01 (20 °C). Solubility: Practically insoluble in water. In hexane 0.655 g/ml, methanol 72.0 ml/ml (both 20 °C). Stability: Decomposed by u.v. light. Hydrolysed in alkaline media. F.p.: 87 °C APPLICATIONS Mode of action: Non-systemic insecticide with contact, stomach, and respiratory action. Gives rapid knockdown. Paralyses insects before killing them. Uses: Control of flies, mosquitoes, ants, and other household and public health insect pests. Often used in combination with piperonyl butoxide or other synergists, for control of chewing and sucking insects on ornamentals, vegetables, and other crops; for household and public health insect control; for insect control in animal houses; and as an animal ectoparasiticide. Formulation types: AE; EC; DP; WP; Coil. Compatibility: Incompatible with alkaline materials. Selected tradenames: Pynamin Forte MAMMALIAN TOXICOLOGY Oral: Acute oral LD50 for male rats 2150, female rats 900 mg/kg. Skin and eye: Acute percutaneous LD50 for male rabbits 2660, female rabbits 4390 mg/kg. Inhalation: LC50 for rats >3875 mg/m3 air. Toxicity class: WHO (a.i.) III; EPA (formulation) III EC hazard: Xn; R22 ECOTOXICOLOGY Birds: LC50 (8 d) for mallard ducks and bobwhite quail 5620 mg 'Pynamin Forte' /kg diet. Fish: LC50 (96 h) for carp 0.134 mg/l. ENVIRONMENTAL FATE Animals: In mammals, following oral administration, one of the two terminal methyl groups of the chrysanthemic acid moiety is oxidised in the liver to an alcohol group, and further to a carboxyl group.