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Fensulfothion: Difference between revisions

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'''Fensulfothion''' is an ] and ].<ref>, alanwood.net</ref> It is highly toxic and listed as an ].<ref></ref> '''Fensulfothion''' is an ] and ].<ref>, alanwood.net</ref> It is highly toxic and listed as an ].<ref></ref> It is widely used on corn, onions, rutabagas, pineapple, bananas, sugar cane, sugar beets, pea nuts, etc.<ref>{{cite journal|last=Sunil Paul|first=M.M.|coauthors=Aravind, Usha K.; Pramod, G.; Aravindakumar, C.T.|title=Oxidative degradation of fensulfothion by hydroxyl radical in aqueous medium|journal=Chemosphere|year=2013|month=April|volume=91|issue=3|pages=295–301|doi=10.1016/j.chemosphere.2012.11.033|url=http://www.sciencedirect.com/science/article/pii/S0045653512014385|accessdate=2 December 2013}}</ref>


==References== ==References==

Revision as of 05:28, 2 December 2013

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
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.

References

  1. Fensulfothion, NIOSH Pocket Guide to Chemical Hazards
  2. Fensulfothion, alanwood.net
  3. Appendix A List of Extremely Hazardous Chemicals
  4. Sunil Paul, M.M. (2013). "Oxidative degradation of fensulfothion by hydroxyl radical in aqueous medium". Chemosphere. 91 (3): 295–301. doi:10.1016/j.chemosphere.2012.11.033. Retrieved 2 December 2013. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help); Unknown parameter |month= ignored (help)


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