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| Product Name: | Chlorfenapyr 24% SC | Appearance: | Off-white Liquid |
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| 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 |
| High Light: | phantom pest control,chemical insecticides |
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organophosphate insecticides / pesticide / chlorfenapyr 24% SC
Our product features:
1) Good quality
2) Customiszed production;
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4) Professional design labels, paper boxes, carton and related packaging .
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.
APPLICATIONS:
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.
| Product name | Chlorfenapyr 24%SC |
| Appearance | Off-white liquid |
| CAS No. | 122453–73–0 |
| Molecular formula | C15H11BrClF3N2O |
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Chemical name
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4-bromo-2-(4-chlorophenyl)-1-ethoxymethyl-5-trifluoromethylpyrrole-3-carbonitrile (IUPAC) |
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Structural Formula
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| 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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