Cinoxate
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| Names | |
|---|---|
| IUPAC name 2-Ethoxyethyl 3-(4-methoxyphenyl)propenoate | |
| Other names 2-Ethoxyethyl p-methoxycinnamate | |
| Identifiers | |
| 104-28-9  | |
| 3D model (Jmol) | Interactive image | 
| ChEMBL | ChEMBL2104045  | 
| ChemSpider | 4523729  | 
| ECHA InfoCard | 100.002.901 | 
| KEGG | D03512  | 
| PubChem | 5373773 | 
| UNII | 5437O7N5BH  | 
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| Properties | |
| C14H18O4 | |
| Molar mass | 250.29 g·mol−1 | 
| Density | 1.102 g/cm3 | 
| Melting point | −25 °C (−13 °F; 248 K) | 
| Boiling point | 184 to 187 °C (363 to 369 °F; 457 to 460 K) at 2 mmHg | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
|  verify (what is   ?) | |
| Infobox references | |
Cinoxate is an organic compound used as an ingredient in some types of sunscreens. It is an ester formed from methoxycinnamic acid and 2-ethoxyethanol. It is a slightly yellow viscous liquid that is insoluble in water, but miscible with alcohols, esters, and vegetable oils.
It protects skin against the sun by absorbing UV-A and UV-B rays.
See also
- Amiloxate, another methoxycinnamate-based sunscreen
- Octyl methoxycinnamate, another methoxycinnamate-based sunscreen
References
- ↑ Merck Index, 11th Edition, 2312.
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