Hexafluoropropylene
Hexafluoropropylene is a compound with the formula C3F6. It is a fluorocarbon alkene in which all of the hydrogen atoms in propylene are replaced by fluorine atoms. It is used as a chemical intermediate.[1] It can be produced by pyrolysis of tetrafluoroethylene or chlorodifluoromethane, or produced from various chlorofluorocarbons [2]
| |||
Names | |||
---|---|---|---|
IUPAC name
Hexafluoropropene | |||
Other names
Perfluoropropene, Perfluoropropylene, freon R 1216, halocarbon R 1216, fluorocarbon 1216 | |||
Identifiers | |||
3D model (JSmol) |
|||
ChemSpider | |||
ECHA InfoCard | 100.003.753 | ||
EC Number |
| ||
PubChem CID |
|||
RTECS number |
| ||
UNII | |||
UN number | 1858 | ||
CompTox Dashboard (EPA) |
|||
| |||
| |||
Properties | |||
C3F6 | |||
Molar mass | 150.023 g·mol−1 | ||
Appearance | Colorless, odorless gas | ||
Density | 1.332 g/ml, liquid at 20 °C | ||
Melting point | −153 °C (−243 °F; 120 K) | ||
Boiling point | −28 °C (−18 °F; 245 K) | ||
Insoluble | |||
Hazards | |||
Main hazards | Suffocation | ||
GHS pictograms | |||
GHS Signal word | Warning | ||
GHS hazard statements |
H280, H332, H335, H351, H371, H373 | ||
P201, P202, P260, P261, P264, P270, P271, P281, P304+312, P304+340, P308+313, P309+311, P312, P314, P403+233, P405, P410+403, P501 | |||
NFPA 704 (fire diamond) | |||
Flash point | Non flammable gas | ||
Related compounds | |||
Related alkenes; organofluorides |
propylene; Hexafluoroacetone, Hexafluoro-2-propanol | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
Infobox references | |||
This is a gaseous phase effluent from the decomposition of teflon when laser cutting it. [3]
References
- Lehmler, HJ (March 2005). "Synthesis of environmentally relevant fluorinated surfactants—a review". Chemosphere. 58 (11): 1471–96. doi:10.1016/j.chemosphere.2004.11.078. PMID 15694468.
- United States patent (expires 5-20-2020) 5043491A, James L. Webster, Elrey L. McCann, Douglas W. Bruhnke, Jan J. Lerou, "Multistep synthesis of hexafluoropropylene", published 1991-08-27, issued 1991-08-27, assigned to E. I. Du Pont de Nemours and Company
- "Laser cutting teflon". Universal Laser Systems, Inc.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.