Misplaced Pages

This is an old revision of this page, as edited by RjwilmsiBot (talk | contribs) at 02:16, 16 February 2011 (Per WP:ISBN formatted 1 ISBNs using AWB (7596)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

O-Ethyl methylphosphonothioic acid

Names
IUPAC name O-ethyl hydrogen methylphosphonothioate
Other names Methyl-phosphonothioic acid O-ethyl ester
Identifiers
CAS Number	18005-40-8
3D model (JSmol)	Interactive image
ChemSpider	483881
ECHA InfoCard	100.150.755
PubChem CID	556615
CompTox Dashboard (EPA)	DTXSID50864811
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). Y verify (what is  ?) Infobox references

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

This article about an organic compound is a stub. You can help Misplaced Pages by expanding it.

• v
• t
• e

• Phosphonothioates
• Organic compound stubs