Perfluoromethylcyclohexane
 | |
| Names | |
|---|---|
| IUPAC name
1,1,2,2,3,3,4,4,5,5,6-Undecafluoro-6-(trifluoromethyl)cyclohexane | |
| Other names
Flutec PP2 | |
| Identifiers | |
| 355-02-2 | |
| 3D model (Jmol) | Interactive image |
| ChemSpider | 9260  |
| EC Number | 206-386-9 |
| PubChem | 9637 |
| |
| |
| Properties | |
| C7F14 | |
| Molar mass | 350.05 g·mol−1 |
| Appearance | Clear, colorless liquid |
| Density | 1.788 g/mL |
| Melting point | −37 °C (−35 °F; 236 K) |
| Boiling point | 76 °C (169 °F; 349 K) |
| 10 ppm | |
| Hazards | |
| Main hazards | None |
| Flash point | None |
| None | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Perfluoromethylcyclohexane is a fluorocarbon liquid—a perfluorinated derivative of the hydrocarbon methylcyclohexane. It is chemically and biologically inert.
Manufacture
Perfluoromethylcyclohexane can be manufactured by the Fowler process, which involves moderating the action of elemental fluorine with cobalt fluoride in the gas phase from toluene. This is preferred as the starting material over methylcyclohexane as less fluorine is required.[1]
Properties
Perfluoromethylcyclohexane is chemically inert and thermally stable (to over 400°C). It is non-toxic.[2]
It is a clear, colorless liquid, with a relatively high density, low viscosity and low surface tension that will rapidly evaporate. It is a relatively good solvent for gases, but a poor solvent for solids and liquids.[3]
In common with other cyclic perfluorocarbons, perfluoromethylcyclohexane can be detected at extremely low concentrations, making it ideal as a tracer.[4]
Applications
- Heat transfer agent
- Dielectric fluid
- Perfluorocarbon tracer
References
- ↑ Sandford G (2003). "Perfluoroalkanes". Tetrahedron. 59: 437–454. doi:10.1016/s0040-4020(02)01568-5.
- ↑ "FLUTEC PP2". F2 Chemicals.
- ↑ "Solubility in Liquids" (PDF). F2 Chemicals.
- ↑ Begley P1, Foulger B, Simmonds P. (1988). "Femtogram detection of perfluorocarbon tracers using capillary gas chromatography-electron-capture negative ion chemical ionisation mass spectrometry.". J Chromatogr. 445 (1): 119–128. doi:10.1016/s0021-9673(01)84513-1.