FC-75
 | |
| Names | |
|---|---|
| IUPAC name
2,2,3,3,4,4,5-heptafluoro-5-(1,1,2,2,3,3,4,4,4-nonafluorobutyl)tetrahydrofuran | |
| Other names
Perfluorocyclic ether, Fluorinert FC-75, Perfluoro-compound FC-75, Perfluoro-2-n-butyl THF, Perfluoro(butyltetrahydrofuran) | |
| Identifiers | |
335-36-4  | |
| 3D model (Jmol) | Interactive image |
| Abbreviations | PFBTHF |
| ECHA InfoCard | 100.005.809 |
| EC Number | 206-389-5 |
| PubChem | 78976 |
| |
| Properties | |
| C8F16O | |
| Molar mass | 416.06 |
| Melting point | −88 °C (−126 °F; 185 K) |
| Boiling point | 102 °C (216 °F; 375 K) |
| Insoluble | |
| 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 | |
FC-75 is a fluorocarbon derivative of tetrahydrofuran with the chemical formula C8F16O. It is practically insoluble in water.
It is one of the 3M Fluorinert fluids. It is used as an inert coolant fluid in electronics and other applications, and as a solvent. FC-75 can be synthesized by the same electrochemical fluorination process used to produce PFOA.[1] However, other perfluorinated ether isomers will also result.
- H(CH2)7COCl + HF → H(CH2)7COF + C7H16 + 2C8F16O + HCl + H2
A similar fluorocarbon-based coolant and solvent is perfluorohexane.
References
- ↑ Savu, P (1994). "Fluorinated Higher Carboxylic Acids". Kirk-Othmer Encyclopedia of Chemical Terminology. John Wiley & Sons, Inc. doi:10.1002/0471238961.0612211519012221.a01.
This article is issued from Wikipedia - version of the 9/2/2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.