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'''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=MM|coauthors=Aravind, UK; Pramod, G; Aravindakumar, CT|title=Oxidative degradation of fensulfothion by hydroxyl radical in aqueous medium.|journal=Chemosphere|date= |
'''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=MM|coauthors=Aravind, UK; Pramod, G; Aravindakumar, CT|title=Oxidative degradation of fensulfothion by hydroxyl radical in aqueous medium.|journal=Chemosphere|date=April 2013|year=2013|volume=91|issue=3|pages=295–301|doi=10.1016/j.chemosphere.2012.11.033|pmid=23273737|url=http://www.sciencedirect.com/science/article/pii/S0045653512014385}}</ref> | ||
==References== | ==References== |
Revision as of 08:09, 23 December 2013
Names | |
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IUPAC name O,O-Diethyl O- phosphorothioate | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.003.741 |
PubChem CID | |
CompTox Dashboard (EPA) | |
InChI
| |
SMILES
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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 |
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
- Fensulfothion, NIOSH Pocket Guide to Chemical Hazards
- Fensulfothion, alanwood.net
- Appendix A List of Extremely Hazardous Chemicals
- Sunil Paul, MM (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.
{{cite journal}}
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