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| Lufenuron |
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| NOMENCLATURE Lufenuron
Common name lufenuron (BSI, pa E-ISO, INN) IUPAC name (RS)-1-[2,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]-3-(2,6-difluorobenzoyl)urea Chemical Abstracts name N-[[[2,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]amino]carbonyl]-2,6-difluorobenzamide CAS RN [103055-07-8] Development codes CGA 184699 (Ciba-Geigy) PHYSICAL CHEMISTRY Lufenuron Composition Tech. is ³98%. Mol. wt. 511.2 M.f. C17H8Cl2F8N2O3 Form Colourless crystals. M.p. 168.7-169.4 ÂC (OECD 102) V.p. <4  10-3 mPa (25 ºC) (OECD 104) KOW logP = 5.12 (25 ºC) (OECD 117) Henry <3.41  10-2 Pa m3 mol-1 (calc.) S.g./density 1.66 at 20 ºC (OECD 109) Solubility In water <0.06 mg/l (25 ºC). In ethanol 41, acetone 460, toluene 72, n-hexane 0.13, n-octanol 8.9 (all in g/l, 25 ºC). Stability Stable in air and light. In water, DT50 32 d (pH 9), 70 d (pH 7), 160 d (pH 5). pKa >8.0 APPLICATIONS Lufenuron Biochemistry Inhibits chitin synthesis. Mode of action Acts mostly by ingestion; larvae are unable to moult, and also cease feeding. Uses Insect growth regulator for control of Lepidoptera and Coleoptera larvae on cotton, maize and vegetables; and citrus whitefly and rust mites on citrus fruit, at 10-50 g/ha. Also for the prevention and control of flea infestations on pets. Formulation types EC. Compatibility Not compatible with pesticides with alkaline reaction (lime sulfur, copper). Selected tradenames: 'Match' (Syngenta) MAMMALIAN TOXICOLOGY Lufenuron |
Brodifacoum
Bromadiolone
Chlorophacinone
Indoxacarb
Browse Products : A B C D E F G H I J K L M N O P Q R S T U V W X Y
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