3-Hexanol
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| Names | |
|---|---|
| IUPAC name
3-Hexanol | |
| Other names
Hexan-3-ol, ethyl propyl carbinol | |
| Identifiers | |
| 17015-11-1 | |
| ChEMBL | ChEMBL46678 |
| ChemSpider | 11678 |
| Jmol interactive 3D | Image |
| PubChem | 12178 |
| UNII | I1ZTO95J84 |
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| Properties | |
| C6H14O | |
| Molar mass | 102.174 g/mol |
| Appearance | colorless liquid |
| Density | 0.819 g/cm3 |
| Boiling point | 135 °C (275 °F; 408 K) |
| 16 g/L | |
| Solubility | miscible with diethyl ether; very soluble in ethanol, acetone |
| Thermochemistry | |
| 286.2 J·mol−1·K−1 (liquid) | |
| Std enthalpy of formation (ΔfH |
-392.4 kJ·mol−1 (liquid) |
| Related compounds | |
| Related compounds |
Hexanol |
| 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 | |
3-Hexanol (IUPAC name, also called ethyl propyl carbinol) is an organic chemical compound. It occurs naturally in the flavor and aroma of plants such as pineapple and is used as a food additive to add flavor.
Reactions
3-Hexanol can be synthesized by the hydroboration of unsaturated hexane compounds such as 3-hexyne.[2]
References
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