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Fensulfothion: Difference between revisions

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Revision as of 00:57, 22 December 2014 editTrappist the monk (talk | contribs)Administrators479,996 editsm Remove redundant |year= parameter from CS1 citations; using AWB← Previous edit Revision as of 20:44, 31 January 2015 edit undoEmily Temple-Wood (NIOSH) (talk | contribs)Autopatrolled, Extended confirmed users, Pending changes reviewers4,912 edits add PELNext edit →
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Revision as of 20:44, 31 January 2015

Fensulfothion
Names
IUPAC name O,O-Diethyl O- phosphorothioate
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.003.741 Edit this at Wikidata
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C11H17O4PS2/c1-4-13-16(17,14-5-2)15-10-6-8-11(9-7-10)18(3)12/h6-9H,4-5H2,1-3H3Key: XDNBJTQLKCIJBV-UHFFFAOYSA-N
  • InChI=1/C11H17O4PS2/c1-4-13-16(17,14-5-2)15-10-6-8-11(9-7-10)18(3)12/h6-9H,4-5H2,1-3H3Key: XDNBJTQLKCIJBV-UHFFFAOYAH
SMILES
  • S=P(Oc1ccc(cc1)S(=O)C)(OCC)OCC
Properties
Chemical formula C11H17O4PS2
Molar mass 308.35 g·mol
Appearance Brown liquid or yellow oil
Hazards
NIOSH (US health exposure limits):
PEL (Permissible) none
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Fensulfothion is an insecticide and nematicide. It is highly toxic and listed as an extremely hazardous substance. It is widely used on corn, onions, rutabagas, pineapple, bananas, sugar cane, sugar beets, pea nuts, etc.

External Links

References

  1. Fensulfothion, NIOSH Pocket Guide to Chemical Hazards
  2. NIOSH Pocket Guide to Chemical Hazards. "#0284". National Institute for Occupational Safety and Health (NIOSH).
  3. Fensulfothion, alanwood.net
  4. Appendix A List of Extremely Hazardous Chemicals
  5. Sunil Paul, MM; Aravind, UK; Pramod, G; Aravindakumar, CT (April 2013). "Oxidative degradation of fensulfothion by hydroxyl radical in aqueous medium". Chemosphere. 91 (3): 295–301. doi:10.1016/j.chemosphere.2012.11.033. PMID 23273737.


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