3-Ethyl-3-pentanol
| Names | |
|---|---|
| Preferred IUPAC name
 3-Ethylpentan-3-ol  | |
| Other names
 Triethylcarbinol; 1,1-Diethyl-1-propanol; 3-Ethyl-3-hydroxypentane; Triethylmethanol  | |
| Identifiers | |
3D model (JSmol)  | 
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| ChemSpider | |
| ECHA InfoCard | 100.009.003 | 
PubChem CID  | 
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| UNII | |
CompTox Dashboard (EPA)  | 
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| Properties | |
| C7H16O | |
| Molar mass | 116.204 g·mol−1 | 
| Appearance | Clear liquid | 
| Density | 0.82 g/cm3 | 
| Boiling point | 140–142 °C (284–288 °F; 413–415 K) | 
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 
Infobox references  | |
3-Ethyl-3-pentanol, also known as 3-ethylpentan-3-ol, is a tertiary alcohol with the molecular formula C7H16O.
It reacts with chromic acid by first dehydrating to an olefin 3-ethyl-2-pentene, and then by converting the double bond to an epoxide.
Perfluorination affords perfluorotriethylcarbinol, a powerful uncoupling agent.