Hexyl cinnamaldehyde
| Structural formula | ||||||||||||||||
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| Structural formula of the ( E ) isomer | ||||||||||||||||
| General | ||||||||||||||||
| Surname | Hexyl cinnamaldehyde | |||||||||||||||
| other names | ||||||||||||||||
| Molecular formula | C 15 H 20 O | |||||||||||||||
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| properties | ||||||||||||||||
| Molar mass | 216.32 g mol −1 | |||||||||||||||
| Physical state |
liquid |
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| density |
0.95 g cm −3 (25 ° C) |
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| boiling point |
174-176 ° C (15 mmHg) |
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| Refractive index |
1.55 |
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| 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 | ||||||||||||||||
Hexylcinnamaldehyde , also hexylcinnamal or hexylcinnamaldehyde , is used as a flavoring in the perfume and cosmetics industries. The substance is suspected of causing allergies .
Occurrence
There are natural occurrences, among other things, in the essential oils of chamomile .
properties
It is a light yellow to yellow, clear liquid that is insoluble in water but soluble in oils.
Individual evidence
- ↑ Entry on HEXYL CINNAMAL in the CosIng database of the EU Commission, accessed on July 29, 2020.
- ↑ a b c d e data sheet α-Hexylcinnamaldehyde, ≥95% from Sigma-Aldrich , accessed on October 7, 2011 ( PDF ).
- ↑ Federal Environment Agency: Fragrances that are suspected of causing allergies