3-hexanol
| Structural formula | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
||||||||||||||||
| ( R ) -3-hexanol (top) and ( S ) -3-hexanol (bottom) | ||||||||||||||||
| General | ||||||||||||||||
| Surname | 3-hexanol | |||||||||||||||
| other names |
|
|||||||||||||||
| Molecular formula | C 6 H 14 O | |||||||||||||||
| Brief description |
flammable, not very volatile liquid |
|||||||||||||||
| External identifiers / databases | ||||||||||||||||
|
||||||||||||||||
| properties | ||||||||||||||||
| Molar mass | 102.18 g mol −1 | |||||||||||||||
| Physical state |
liquid |
|||||||||||||||
| density |
0.82 g cm −3 |
|||||||||||||||
| Melting point |
6 ° C |
|||||||||||||||
| boiling point |
135 ° C |
|||||||||||||||
| Vapor pressure |
4.66 h Pa (20 ° C) |
|||||||||||||||
| solubility |
|
|||||||||||||||
| Refractive index |
1.415 (20 ° C) |
|||||||||||||||
| safety instructions | ||||||||||||||||
|
||||||||||||||||
| As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C | ||||||||||||||||
3-Hexanol is a chemical compound from the group of secondary alcohols . It is one of the 17 structural isomers of hexanols . The compound occurs in two stereoisomeric forms. Whenever “3-hexanol” is mentioned in the scientific literature or in this article without any further addition, one always means the racemate , i.e. ( RS ) - (±) -3-hexanol, a 1: 1 mixture of ( R ) - and ( S ) -3-hexanol.
Occurrence
3-Hexanol occurs naturally in some plants such as saffron and lavender, as well as in the fruits of various plants such as bananas and melons.
Extraction and presentation
Racemic 3-hexanol can be obtained by hydroboration of 3-hexene or 3-hexyne .
safety instructions
The compound forms highly flammable vapor-air mixtures. It has a flash point of 41 ° C. The explosion range is between 1.1% by volume (45 g / m 3 ) as the lower explosion limit (LEL) and 7% by volume (298 g / m 3 ) as the upper explosion limit (UEL). The ignition temperature is 305 ° C. It therefore falls into temperature class T2.
Individual evidence
- ↑ a b c d e f g Entry for CAS no. 623-37-0 in the GESTIS substance database of the IFA , accessed on November 30, 2015 (JavaScript required)
- ↑ a b c George A. Burdock, Fenaroli's Handbook of Flavor Ingredients, ISBN 0-8493-3034-3 .
- ↑ a b c 3-Hexanol data sheet from Sigma-Aldrich , accessed on February 21, 2011 ( PDF ).
- ↑ Liber Herbarum .
- ^ E. Brandes, W. Möller: Safety-related parameters - Volume 1: Flammable liquids and gases , Wirtschaftsverlag NW - Verlag für neue Wissenschaft GmbH, Bremerhaven 2003.