Chemistry:1,3-Difluoro-2-propanol
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Names | |||
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Preferred IUPAC name
1,3-Difluoropropan-2-ol | |||
Identifiers | |||
3D model (JSmol)
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Properties | |||
C3H6F2O | |||
Molar mass | 96.077 g·mol−1 | ||
Density | 1.24 g/cm3 (at 25 °C) [1] | ||
Boiling point | 54 to 55 °C (129 to 131 °F; 327 to 328 K) | ||
Hazards | |||
Flash point | 42 °C (108 °F; 315 K) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
verify (what is ?) | |||
Infobox references | |||
Tracking categories (test):
1,3-Difluoro-2-propanol is a metabolic poison which disrupts the citric acid cycle and is used as a rodenticide, similar to sodium fluoroacetate. It is the main ingredient (along with 1-chloro-3-fluoro-2-propanol) in the rodenticide product Gliftor which was widely used in the former USSR[2][3][4] and still approved in China.[5]
References
- ↑ Sigma Aldrich
- ↑ "[Gliftor poisoning]" (in ru). Sudebno-Meditsinskaia Ekspertiza 29 (1): 55–6. 1986. PMID 3961873.
- ↑ "The biochemical toxicology of 1,3-difluoro-2-propanol, the major ingredient of the pesticide gliftor: the potential of 4-methylpyrazole as an antidote". Journal of Biochemical and Molecular Toxicology 12 (1): 41–52. 1998. doi:10.1002/(SICI)1099-0461(1998)12:1<41::AID-JBT6>3.0.CO;2-P. PMID 9414486.
- ↑ "The mode of toxic action of the pesticide gliftor: the metabolism of 1,3-difluoroacetone to (−)-erythro-fluorocitrate". Journal of Biochemical and Molecular Toxicology 15 (1): 47–54. 2001. doi:10.1002/1099-0461(2001)15:1<47::AID-JBT6>3.0.CO;2-E. PMID 11170315.
- ↑ Wood, Alan. "Gliftor". http://www.alanwood.net/pesticides/gliftor.html.
Original source: https://en.wikipedia.org/wiki/1,3-Difluoro-2-propanol.
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