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|Product Name:||Chlorfenapyr 10%SC||Appearance:||Off-white Liquid|
|Application::||Agrochemicals & Pesicides||Vapour Pressure:||<10*10∧(-7)(25°C)|
|Stability:||Soluble In Acetone, Solubility In Non- Ion Water Is 0.13-0.14(pH7)||CAS No.:||122453-73-0|
organic insect killer
organophosphate insecticides / pesticide / chlorfenapyr 10% SC
Biochemistry Oxidative removal in vivo of the N-ethoxymethyl group generates the active species, which is a mitochondrial uncoupler. Mode of action Insecticide and acaricide with mainly stomach and some contact action. Exhibits good translaminar but limited systemic activity in plants.
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Chlorfenapyr Uses Control of many species of insects and mites, including those resistant to carbamate, organophosphate and pyrethroid insecticides and also chitin-synthesis inhibitors, in cotton, vegetables, citrus, top fruit, vines and soya beans. Among pests resistant to conventional products which are controlled by chlorfenapyr are Brevipalpus phoenicis (leprosis mite), Leptinotarsa decemlineata (Colorado potato beetle), Helicoverpa spp., Heliothis spp., Plutella xylostella (diamond-back moth) and Tetranychus spp. Also control of many species of structural and household Formicidae (especially Camponotus, Iridomyrmex, Monomorium and Solenopsis spp.), Blattellidae (especially Blatta, Blattella, Periplaneta and Supella spp.), Kalotermitidae (especially Incisitermes spp.) and Rhinotermitidae (especially Reticulitermes, Coptotermes and Heterotermes spp.), at use rates of between 0.125% to 0.50% a.i. w/w.
|Product name||Chlorfenapyr 36%SC|
|Biochemistry||Oxidative removal in vivo of the N-ethoxymethyl group generates the active species, which is a mitochondrial uncoupler.|
|Mode of action||Insecticide and acaricide with mainly stomach and some contact action. Exhibits good translaminar, but limited systemic, activity in plants.|
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