Fensulfothion

Fensulfothion
Names
	IUPAC name O,O-Diethyl O-[4-(methylsulfinyl)phenyl] phosphorothioate
Identifiers
CAS Number	115-90-2 ;
3D model (JSmol)	Interactive image;
ChemSpider	7991;
ECHA InfoCard	100.003.741
PubChem CID	8292;
UNII	VB39B105PO ;
CompTox Dashboard (EPA)	DTXSID6021953 ;
	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,4-5H2,1-3H3 Key: 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,4-5H2,1-3H3 Key: XDNBJTQLKCIJBV-UHFFFAOYAH;
	SMILES S=P(Oc1ccc(cc1)S(=O)C)(OCC)OCC;
Properties
Chemical formula	C11H17O4PS2
Molar mass	308.35 g·mol−1
Appearance	Brown liquid or yellow oil[1]
Density	1.20 g/mL (20°C)[1]
Solubility in water	0.2% (25°C)
Hazards
Main hazards	combustible[1]
	NIOSH (US health exposure limits):
PEL (Permissible)	none[1]
REL (Recommended)	TWA 0.1 mg/m3[1]
IDLH (Immediate danger)	N.D.[1]
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Fensulfothion is an insecticide and nematicide. It is highly toxic and listed as an extremely hazardous substance.[2] It is widely used on corn, onions, rutabagas, pineapple, bananas, sugar cane, sugar beets, pea nuts, etc.[3]

External links

Fensulfothion in the Pesticide Properties DataBase (PPDB)

References

NIOSH Pocket Guide to Chemical Hazards. "#0284". National Institute for Occupational Safety and Health (NIOSH).
Appendix A List of Extremely Hazardous Chemicals
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. Bibcode:2013Chmsp..91..295S. doi:10.1016/j.chemosphere.2012.11.033. PMID 23273737.

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[PGCH-1] NIOSH Pocket Guide to Chemical Hazards. "#0284". National Institute for Occupational Safety and Health (NIOSH).

[2] Appendix A List of Extremely Hazardous Chemicals

[3] 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. Bibcode:2013Chmsp..91..295S. doi:10.1016/j.chemosphere.2012.11.033. PMID 23273737.