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cinoxate

Structure via PubChem · Public domain (PubChem)

EntityQ2319112· pop 10· linked from 41 articles

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.

In the Vinony graph

Within Vinony's link graph, cinoxate is referenced by 41 other articles, and connects out to alcohols, ultraviolet radiation and mass density.

It is catalogued under topics including 4-Methoxyphenyl compounds, Chembox image size set and Cinnamate esters.

Its subject is documented across 9 Wikipedia language editions.

Chemical data

Formula
C14H18O4
Molecular weight
250.29 g/mol
IUPAC name
2-ethoxyethyl (E)-3-(4-methoxyphenyl)prop-2-enoate
SMILES
CCOCCOC(=O)/C=C/C1=CC=C(C=C1)OC
InChIKey
CMDKPGRTAQVGFQ-RMKNXTFCSA-N
XLogP
2.4
Polar surface area
44.8 Ų
H-bond donors
0
H-bond acceptors
4
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 2
Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
250.121
Show 5 more facts
chemical formula
C₁₄H₁₈O₄
isomeric SMILES
CCOCCOC(=O)/C=C/C1=CC=C(C=C1)OC
canonical SMILES
CCOCCOC(=O)C=CC1=CC=C(C=C1)OC
medical condition treated
photodermatitis
Commons category
Cinoxate
Sources (1)

via Wikidata · CC0

~1 min read

Encyclopedic overview

2 sections
Contents
  • See also
  • 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 was approved as UV filter in the USA by the FDA in 1961, but it is not commonly used in cosmetic formulations anymore.

Excerpted from Wikipedia’s “cinoxate” article, available under the CC BY-SA 4.0 licence.

Available in 9 languages

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