Cinoxate

Cinoxate

Ball-and-stick model of the cinoxate molecule
Space-filling model of the cinoxate molecule
Names
IUPAC name 2-Ethoxyethyl 3-(4-methoxyphenyl)propenoate
Other names 2-Ethoxyethyl p-methoxycinnamate
Identifiers
CAS Number	104-28-9 Y
ChEMBL	ChEMBL2104045 N
ChemSpider	4523729 Y
Jmol 3D model	Interactive image
KEGG	D03512 Y
PubChem	5373773
UNII	5437O7N5BH Y
InChI InChI=1S/C14H18O4/c1-3-17-10-11-18-14(15)9-6-12-4-7-13(16-2)8-5-12/h4-9H,3,10-11H2,1-2H3/b9-6+ Y Key: CMDKPGRTAQVGFQ-RMKNXTFCSA-N Y InChI=1/C14H18O4/c1-3-17-10-11-18-14(15)9-6-12-4-7-13(16-2)8-5-12/h4-9H,3,10-11H2,1-2H3/b9-6+ Key: CMDKPGRTAQVGFQ-RMKNXTFCBV
SMILES O=C(OCCOCC)\C=C\c1ccc(OC)cc1
Properties
Chemical formula	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).
N verify (what is YN ?)
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