trans -2-hexen-1-ol
Structural formula | ||||||||||
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General | ||||||||||
Surname | trans -2-hexen-1-ol | |||||||||
other names |
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Molecular formula | C 6 H 12 O | |||||||||
Brief description |
yellow liquid |
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properties | ||||||||||
Molar mass | 100.16 g mol −1 | |||||||||
Physical state |
liquid |
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density |
0.84 g cm −3 (20 ° C) |
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boiling point |
158-160 ° C |
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Vapor pressure |
6.3 hPa (20 ° C) |
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solubility |
poorly soluble in water (20 ° C) |
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Refractive index |
1.4343 (20 ° C, 589 nm) |
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safety instructions | ||||||||||
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Toxicological data | ||||||||||
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 |
trans -2-hexen-1-ol is a chemical compound from the group of unsaturated aliphatic alcohols and isomeric to cis -2-hexen-1-ol .
Occurrence
The compound occurs naturally in raspberries, oranges, apples, green tea, kiwis, peaches, strawberries, and tomatoes. It is one of the green leaf fragrances .
Extraction and presentation
trans -2-hexen-1-ol can be obtained by reducing trans -2-hexenal .
properties
It concerns with trans -2-hexene-1-ol to a yellowish liquid that is poorly soluble in water. It has a green-fruity to pungent odor.
use
trans -2-hexen-1-ol is used as an odorous substance in the cosmetics and food industries.
Individual evidence
- ↑ a b c d e f g h i j k l data sheet trans-2-hexen-1-ol (PDF) from Merck , accessed on April 3, 2012.
- ↑ Data sheet trans-2-hexen-1-ol, ≥96%, FCC, FG from Sigma-Aldrich , accessed on April 3, 2012 ( PDF ).
- ^ David Rowe: Chemistry and Technology of Flavors and Fragrances . John Wiley & Sons, 2009, ISBN 978-1-4051-4807-8 , pp. 57 ( limited preview in Google Book search).
- ↑ Mechthild Busch-Stockfisch: Practical Guide to Sensor Technology in Product Development and Quality Assurance . Behr's Verlag, 2007, ISBN 978-3-86022-958-3 , pp. 21 ( limited preview in Google Book search).
- ↑ (E) -2-hexen-1-ol 928-95-0. The Good Scents Company, July 16, 2015, accessed May 18, 2017 .