A | B | C | D | E | F | G | H | CH | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9
Names | |
---|---|
Preferred IUPAC name
Hexan-3-ol | |
Other names
3-Hexanol
Ethyl propyl carbinol | |
Identifiers | |
3D model (JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.009.810 |
PubChem CID
|
|
UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
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 | |
Heat capacity (C)
|
286.2 J·mol−1·K−1 (liquid) |
Std enthalpy of
formation (ΔfH⦵298) |
-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 , 100 kPa).
|
3-Hexanol (IUPAC name: hexan-3-ol; 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
- ^ Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, Florida: CRC Press, pp. 3–310, 5–47, 8–106, ISBN 0-8493-0594-2
- ^ Burdock, George A. (2005), Fenaroli's handbook of flavor ingredients, Boca Raton, Fla.: CRC Press, p. 786, ISBN 0-8493-3034-3
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