Propoxur
| Names | |
|---|---|
| Preferred IUPAC name
2-[(Propan-2-yl)oxy]phenyl methylcarbamate | |
| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.003.676 |
| KEGG | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C11H15NO3 | |
| Molar mass | 209.245 g·mol−1 |
| Appearance | White to tan crystalline powder |
| Odor | faint, characteristic |
| Melting point | 86 to 92 °C; 187 to 197 °F; 359 to 365 K |
| Boiling point | decomposes |
| 0.2% (20°C) | |
| Vapor pressure | 0.0000937 mmHg (20 °C) |
| Pharmacology | |
| QP53AE02 (WHO) | |
| Hazards | |
| Flash point | > 149 °C; 300 °F; 422 K |
| NIOSH (US health exposure limits): | |
PEL (Permissible)
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none |
REL (Recommended)
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TWA 0.5 mg/m3 |
IDLH (Immediate danger)
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N.D. |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Propoxur is a carbamate, non-systemic, synthetic insecticide, produced from catechol, and was introduced in 1959 by Bayer.