Skip to content
[P]pubcas
Independent chemical reference Compare
Chemical substance record

Oxybenzone

131-57-7C14H12O3228.247 g/mol

A hydroxybenzophenone that is benzophenone which is substituted at the 2- and 4-positions of one of the benzene rings by hydroxy and methoxy groups respectively. — ChEBI

Safety references

Safety documents & references

1 indexed references
JP · NITE

Government GHS classification

R04-C-041-JNIOSH, MOE · FY2022

View classification

Find a product-specific SDS

Safety guides and government classification records are not a manufacturer’s SDS. Match supplier, product number, concentration, physical form, region and revision before using a document.

Identity & molecular properties

Source-linked values
CAS number131-57-7ChEBI ↗
Molecular formulaC14H12O3ChEBI ↗
Molar mass228.247 g/molChEBI ↗
Monoisotopic mass228.07864 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:34283ChEBI ↗

Cross-source molecular data

PubChem
Molar mass228.24 g/molPubChem ↗
Exact mass228.078644241 DaPubChem ↗
Computed XLogP3.6PubChem ↗
Topological polar surface area (Ų)46.5PubChem ↗
H-bond donors1PubChem ↗
H-bond acceptors3PubChem ↗
Rotatable bonds3PubChem ↗

PubChem computed values are shown separately from the ChEBI record. An exact InChIKey match was used to connect the records. Molecular descriptors do not describe a supplied product’s purity, particle size or performance.

Names & structural identifiers

Copy any identifier
oxybenzone
(2-hydroxy-4-methoxyphenyl)(phenyl)methanone
DXGLGDHPHMLXJC-UHFFFAOYSA-N
COc1ccc(C(=O)c2ccccc2)c(O)c1
InChI=1S/C14H12O3/c1-17-11-7-8-12(13(15)9-11)14(16)10-5-3-2-4-6-10/h2-9,15H,1H3

Names & synonyms

(2-hydroxy-4-methoxyphenyl)(phenyl)methanoneoxibenzonaoxybenzonum

Names are supplied by ChEBI. Trade names and related synonyms may describe a broader product context.

Classification & relationships

ChEBI ontology

Roles recorded in ChEBI

xenobioticdermatologic drugprotective agentultraviolet filterenvironmental contaminant

Database role annotations describe reported biological or chemical roles; they are not product approvals or recommendations for use.

Safety classification · Japan

NITE / Japanese government
Japan · FY2022 source classification
(2-Hydroxy-4-methoxyphenyl)(phenyl)methanone · R04-C-041-JNIOSH, MOE
EndpointReported classification
Reproductive toxicityCategory 2
Hazardous to the aquatic environment (Acute)Category 1
Hazardous to the aquatic environment (Long-term)Category 1

Selected source-reported endpoints. Other endpoints, rationales and conditions remain in the original classification. Missing or unlisted information does not mean non-hazardous. This is not a global classification or transport decision.

Read the original NITE classification

Mass ↔ amount of substance

Calculated from sourced mass
Equivalent amount
0.00438122 mol

Uses 228.247 g/mol from ChEBI. Assumes the substance described by this record; no purity or concentration correction is applied.

Elemental composition

Theoretical mass fractions
C
Carbon · 14 atoms
73.67%
O
Oxygen · 3 atoms
21.03%
H
Hydrogen · 12 atoms
5.30%

Calculated theoretical mass fractions from the reported formula and PubChem periodic-table atomic masses. These are not assay or purity results.

Research & patent references

Selected source associations
Five cases of photocontact dermatitis due to topical ketoprofen: photopatch testing and cross-reaction study. ↗Photodermatology, photoimmunology & photomedicine · 2001 Feb · PMID 11169173
US2773903 · Patent reference ↗Patent cross-reference supplied by ChEBI. Association alone does not establish claim scope.
US2861104 · Patent reference ↗Patent cross-reference supplied by ChEBI. Association alone does not establish claim scope.
US2861105 · Patent reference ↗Patent cross-reference supplied by ChEBI. Association alone does not establish claim scope.

Sources & record history

Checked 27 Sep 2026
EMBL-EBI ChEBI · CHEBI:34283

Release 255, 9 September 2026. ChEBI three-star (manually annotated) source entry. View original record ↗ · CC BY 4.0

NCBI PubChem · CID 4632 · retrieved 2026-09-27

PubCAS formats source data, connects references and computes explicitly labelled conversions. CAS cross-references are supplied by ChEBI; they do not constitute CAS verification or endorsement.