:Mevinphos
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| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 424730608
| Name = Mevinphos
| ImageFile =Mevinphos E,Z Isomers Formulae V.1.svg
| ImageSize =
| IUPACName = 2-methoxycarbonyl-1-methylvinyl dimethyl phosphate
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|Section1={{Chembox Identifiers
| Abbreviations =
| CASNo = 7786-34-7
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| CASNo_Ref = {{cascite|correct|??}}
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 14ZYO4IKXT
| PubChem = 9560
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 9185
| InChI = 1/C7H13O6P/c1-6(5-7(8)10-2)13-14(9,11-3)12-4/h5H,1-4H3
| InChIKey = GEPDYQSQVLXLEU-UHFFFAOYAN
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C7H13O6P/c1-6(5-7(8)10-2)13-14(9,11-3)12-4/h5H,1-4H3
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = GEPDYQSQVLXLEU-UHFFFAOYSA-N
| EINECS =
| SMILES =CC(=CC(=O)OC)OP(=O)(OC)OC
| Beilstein =
| Gmelin =
| 3DMet =}}
|Section2={{Chembox Properties
| C=7 | H=13 | O=6 | P=1
| Appearance = Colorless liquid{{cite book|editor=Muller, Franz|title=Agrochemicals: Composition, Production, Toxicology, Applications|year=2000|publisher=Wiley-VCH|location=Toronto|isbn=3-527-29852-5}}
| MeltingPtC = 21
| MeltingPt_notes = (E isomer); 6.9 °C (Z isomer)
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| VaporPressure = 0.003 mmHg (20°C)
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|Section3={{Chembox Structure
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|Section4={{Chembox Thermochemistry
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|Section5={{Chembox Pharmacology
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|Section6={{Chembox Explosive
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|Section7={{Chembox Hazards
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| FlashPtF = 347
| AutoignitionPt =
| ExploLimits =
| PEL = TWA 0.1 mg/m3 [skin]{{PGCH|0503}}
| LC50 = 14 ppm (rat, 1 hr){{IDLH|7786347|Phosdrin}}
| LD50 = 3 mg/kg (rat, oral)
4 mg/kg (mouse, oral)
6-7 mg/kg (rat, oral)
| REL = TWA 0.01 ppm (0.1 mg/m3) ST 0.03 ppm (0.3 mg/m3) [skin]
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|Section8={{Chembox Related
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Mevinphos is a toxic organophosphate insecticide that acts as an acetylcholinesterase inhibitor to control insects in a wide range of crops. It was most commonly used for the control of chewing and sucking insects, as well as spider mites. Common synonym names are duraphos, fosdrin, menite, mevinfos, mevinox, phosdrin, and phosdrine. It is not allowed in the EU anymore.{{PPDB|471}}
Manufacture
Mevinphos is produced by the reaction of trimethyl phosphite with chloroacetoacetate.
References
{{reflist}}
Further reading
- {{cite book|editor=Wolverton, B.C.|title=Aquatic Plants for Removal of Mevinphos from the Aquatic Environment; Volume 72720 of NASA Technical memorandum|year=1975|publisher=National Space Technology Laboratories (U.S.)|location=Mississippi}}
External links
- {{PPDB|471}}
{{Insecticides}}
{{Acetylcholine metabolism and transport modulators}}
Category:Acetylcholinesterase inhibitors