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O-Ethyl methylphosphonothioic acid: Difference between revisions

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Chemical often used in the creation of harmful substances
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Find sources: "O-Ethyl methylphosphonothioic acid" – news · newspapers · books · scholar · JSTOR (August 2023)
O-Ethyl methylphosphonothioic acid
Names
Preferred IUPAC name O-Ethyl hydrogen methylphosphonothioate
Other names Methyl-phosphonothioic acid O-ethyl ester
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.150.755 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C3H9O2PS/c1-3-5-6(2,4)7/h3H2,1-2H3,(H,4,7)Key: XXNRHOAJIUSMOQ-UHFFFAOYSA-N
  • InChI=1/C3H9O2PS/c1-3-5-6(2,4)7/h3H2,1-2H3,(H,4,7)Key: XXNRHOAJIUSMOQ-UHFFFAOYAH
SMILES
  • S=P(O)(OCC)C
Properties
Chemical formula C3H9O2PS
Molar mass 140.14 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

O-Ethyl methylphosphonothioic acid (EMPTA) is an organophosphate compound. A dual-use chemical, it has constructive uses in the synthesis of pesticides and pharmaceuticals, and it is also a precursor in the synthesis of nerve agents such as Agent VM and Agent VX. The detection of EMPTA is cited as a major influence in the United States' 1998 decision to destroy the Al-Shifa pharmaceutical factory in Sudan.

References

  1. Claudine McCarthy (2005). "EMPTA (O-Ethyl methylphosphonothioic acid)" (Google Books excerpt). In Eric Croddy, James J. Wirtz (ed.). Weapons of mass destruction: an encyclopedia of worldwide policy, technology, and history. pp. 123–124. ISBN 1-85109-490-3.
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