2-Fluoroethanol
Appearance
![]() | |||
| |||
Names | |||
---|---|---|---|
Other names
Ethylene fluorohydrine
| |||
Identifiers | |||
3D model (JSmol)
|
|||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.006.128 | ||
PubChem CID
|
|||
CompTox Dashboard (EPA)
|
|||
| |||
| |||
Properties | |||
C2H5FO | |||
Molar mass | 64.059 g·mol−1 | ||
Density | 1.1040 g cm−3[1] | ||
Melting point | −26.3 °C (−15.3 °F; 246.8 K)[1] | ||
Boiling point | 103.5 °C (218.3 °F; 376.6 K)[1] | ||
miscible[1] | |||
Vapor pressure | 19 mbar (15 °C)[1] | ||
Acidity (pKa) | 14.42[2] | ||
Hazards | |||
Lethal dose or concentration (LD, LC): | |||
LD50 (median dose)
|
5 mg·kg−1(Rat, oral)[3] 1.10 g·m−3·10min−1 (LC50, Mouse, Inhalation)[3] 0.20 g·m−3·10min−1 (LC50, Rat, Inhalation)[3] | ||
Related compounds | |||
Other anions
|
2-Chloroethanol | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
2-Fluoroethanol is the chemical compound with the formula CH2FCH2OH and the simplest fluorohydrin. This colorless liquid is one of the simplest stable fluorinated alcohols. It was developed for use as a rodenticide, insecticide, and acaricide. Owing to its easy oxidation to fluoroacetic acid, fluoroethanol is highly toxic (LD50 = 10 mg/kg). The related difluoro- and trifluoroethanols are far less dangerous.[4]
See also
References
- ^ a b c d e f Record of CAS RN 371-62-0 in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 18. February 2010.
- ^ Template:ChemID
- ^ a b c MSDS from AlfaAesar
- ^ Günter Siegemund, Werner Schwertfeger, Andrew Feiring, Bruce Smart, Fred Behr, Herward Vogel, Blaine McKusick “Fluorine Compounds, Organic” in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, 2007, Weinheim. doi:10.1002/14356007.a11_349