Phoxim
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| Names | |
|---|---|
| IUPAC name
(E,Z)-N-[(Diethoxyphosphorothioyl)oxy]benzenecarboximidoyl cyanide
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| Other names
Baythion
Valexone Phoxime Sebacil Valexon Volaton | |
| Identifiers | |
3D model (
JSmol ) |
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| ChemSpider | |
ECHA InfoCard
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100.035.337 |
| EC Number |
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| KEGG | |
| MeSH | Phoxim |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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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 )
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| 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).
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Phoxim is an
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
acarids
.
This pesticide should be used with caution since some insects like Helicoverpa assulta become even more resistant when exposed.[4]
References
- ^ "Phoxim PubChem entry". Retrieved 2008-07-06.
- ^ Commission for Veterinary Medicinal Products; Phoxim Summary Report
- ^ COMMISSION DECISION of 21 June 2007 concerning the non-inclusion of certain active substances in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing these substances
- .
