Hexafluoropropylene
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| Names | |||
|---|---|---|---|
| IUPAC name
Hexafluoropropene | |||
| Other names
Perfluoropropene, Perfluoropropylene, freon R 1216, halocarbon R 1216, fluorocarbon 1216 | |||
| Identifiers | |||
| 116-15-4 | |||
| ChemSpider | 8001 | ||
| Jmol interactive 3D | Image | ||
| RTECS number | UD0350000 | ||
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| Properties | |||
| C3F6 | |||
| Molar mass | 150.02 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 | Harmful (Xn) | ||
| R-phrases | R20, R37 | ||
| S-phrases | S41 | ||
| NFPA 704 | |||
| 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). | |||
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| Infobox references | |||
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]
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.
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