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| |
| Names | |
|---|---|
| IUPAC name
(E,Z)-N-[(Diethoxyphosphorothioyl)oxy]benzenecarboximidoyl cyanide | |
| Other names
Baythion | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider |
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| ECHA InfoCard | 100.035.337 
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| EC Number |
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| KEGG |
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| MeSH | Phoxim |
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
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| |
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| 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: | |
  
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| 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 their standard state (at 25 °C [77 °F], 100 kPa). | |
Phoxim is an organophosphate insecticide that is produced by the Bayer corporation. It is an analogous dimethyl ester and an organothiophosphate acaricide. It is allowed for use in limited applications in the European Union.[2] It is banned for use on crops in the European Union since 22 December 2007.[3]
It is used in veterinary medicine to treat ectoparasitic acarids.
This pesticide should be used with caution since some insects like Helicoverpa assulta become even more resistant when exposed.[4]
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