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 | |
| Names | |
|---|---|
| IUPAC name (E,Z)-N-[(Diethoxyphosphorothioyl)oxy]benzenecarboximidoyl cyanide | |
| Other names Baythion Valexone Phoxime Sebacil Valexon Volaton | |
| Identifiers | |
3D model (JSmol) | |
| ChemSpider |
|
| ECHA InfoCard | 100.035.337 |
| EC Number |
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| KEGG |
|
| MeSH | Phoxim |
| UNII | |
| |
| |
| Properties | |
| C12H15N2O3PS | |
| Molar mass | 298.30 g·mol−1 |
| Appearance | Brownish red liquid |
| Density | 1.17 g/cm3 |
| Melting point | 6.1 °C (43.0 °F; 279.2 K) |
| Boiling point | 102 |
| 7 ppm | |
| Pharmacology | |
| QP53AE03 (WHO) | |
| Hazards | |
| GHS labelling: | |
   | |
| Warning | |
| H302,H317,H361f,H410 | |
| P201,P202,P261,P264,P270,P272,P273,P280,P281,P301+P312,P302+P352,P308+P313,P321,P330,P333+P313,P363,P391,P405,P501 | |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
Phoxim is anorganophosphateinsecticide that is produced by theBayer corporation. It is an analogous dimethylester and anorganothiophosphateacaricide. It is allowed for use in limited applications in the European Union.[2] It is banned for use on crops in theEuropean Union since 22 December 2007.[3]
It is used in veterinary medicine to treatectoparasiticacarids.
This pesticide should be used with caution since some insects likeHelicoverpa assulta become even more resistant when exposed.[4]
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