Mevinphos
From Wikipedia, the free encyclopedia
| Names | |
|---|---|
| IUPAC name
2-methoxycarbonyl-1-methylvinyl dimethyl phosphate
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| Identifiers | |
| 26718-65-0 |
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| ChemSpider | 9185 |
| Jmol interactive 3D | Image |
| PubChem | 9560 |
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| Properties | |
| C7H13O6P | |
| Molar mass | 224.15 g·mol−1 |
| Appearance | Colorless liquid[1] |
| Density | 1.25 g/mL[2] |
| Boiling point | 21 °C (70 °F; 294 K) (E isomer); 6.9 °C (Z isomer) |
| miscible[2] | |
| Vapor pressure | 0.003 mmHg (20°C)[2] |
| Hazards | |
| Flash point | 175 °C; 347 °F; 448 K [2] |
| Lethal dose or concentration (LD, LC): | |
|
LD50 (Median dose)
|
3 mg/kg (rat, oral) 4 mg/kg (mouse, oral) 6-7 mg/kg (rat, oral)[3] |
|
LC50 (Median concentration)
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14 ppm (rat, 1 hr)[3] |
| US health exposure limits (NIOSH): | |
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PEL (Permissible)
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TWA 0.1 mg/m3 [skin][2] |
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REL (Recommended)
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TWA 0.01 ppm (0.1 mg/m3) ST 0.03 ppm (0.3 mg/m3) [skin][2] |
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IDLH (Immediate danger
|
4 ppm[2] |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
Mevinphos is an organophosphate insecticide that acts as an acetylcholinesterase inhibitor to control insects in a wide range of crops. It is most commonly used for the control of chewing and sucking insects, as well as spider mites.
Manufacture[edit]
Mevinphos is produced by the reaction of trimethyl phosphite with chloroacetoacetate.[1]
References[edit]
- ^ a b Muller, Franz, ed. (2000). Agrochemicals: Composition, Production, Toxicology, Applications. Toronto: Wiley-VCH. ISBN 3-527-29852-5.
- ^ a b c d e f g "NIOSH Pocket Guide to Chemical Hazards #0503". National Institute for Occupational Safety and Health (NIOSH).
- ^ a b "Phosdrin". Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH).
External Links[edit]
- Mevinphos in the Pesticide Properties DataBase (PPDB)

