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| Names | |
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| Preferred IUPAC name
(2E)-3-Phenylprop-2-en-1-ol | |
| Other names | |
| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.216.224 |
| EC Number |
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| KEGG | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C9H10O | |
| Molar mass | 134.178 g·mol−1 |
| Density | 1.0397 g/cm3 at 35 °C |
| Melting point | 33 °C (91 °F; 306 K) |
| Boiling point | 250 °C (482 °F; 523 K) |
| Slightly | |
| Solubility | soluble in ethanol, acetone, dichloromethane |
| -87.2·10−6 cm3/mol | |
| Hazards | |
| GHS labelling: | |
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| Warning | |
| H317 | |
| P261, P272, P280, P302+P352, P321, P333+P313, P363, P501 | |
| Flash point | 126°C |
| Safety data sheet (SDS) | External MSDS |
| Related compounds | |
Related compounds
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Cinnamic acid; Cinnamaldehyde |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Cinnamyl alcohol or styron[2] is an organic compound that is found in esterified form in storax, Balsam of Peru, and cinnamon leaves. It forms a white crystalline solid when pure, or a yellow oil when even slightly impure. It can be produced by the hydrolysis of storax.
Cinnamyl alcohol is a occurs naturally only in small quantities, so its industrial demand is usually fulfilled by chemical synthesis starting from cinnamaldehyde.[3]
- ^ Merck Index, 11th Edition, 2305
- ^ a b Chemical News and Journal of Industrial Science, Volumes 27-28, Sir William Crookes, page 126
- ^ Zucca, P; Littarru, M; Rescigno, A; Sanjust, E (May 2009). "Cofactor recycling for selective enzymatic biotransformation of cinnamaldehyde to cinnamyl alcohol". Bioscience, Biotechnology, and Biochemistry. 73 (5): 1224–6. doi:10.1271/bbb.90025. PMID 19420690. S2CID 28741979.