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Chemical substance record

Salsalate

552-94-3C14H10O5258.229 g/mol

A dimeric benzoate ester obtained by intermolecular condensation between the carboxy of one molecule of salicylic acid with the phenol group of a second. It is a prodrug for salycylic acid that is used for treatment of rheumatoid arthritis and osteoarthritis and also shows activity against type II diabetes. — ChEBI

Safety references

Safety documents & references

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Identity & molecular properties

Source-linked values
CAS number552-94-3ChEBI ↗
Molecular formulaC14H10O5ChEBI ↗
Molar mass258.229 g/molChEBI ↗
Monoisotopic mass258.05282 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:9014ChEBI ↗

Cross-source molecular data

PubChem
Molar mass258.23 g/molPubChem ↗
Exact mass258.05282342 DaPubChem ↗
Computed XLogP3PubChem ↗
Topological polar surface area (Ų)83.8PubChem ↗
H-bond donors2PubChem ↗
H-bond acceptors5PubChem ↗
Rotatable bonds4PubChem ↗

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
salsalate
2-[(2-hydroxybenzoyl)oxy]benzoic acid
WVYADZUPLLSGPU-UHFFFAOYSA-N
O=C(Oc1ccccc1C(=O)O)c1ccccc1O
InChI=1S/C14H10O5/c15-11-7-3-1-5-9(11)14(18)19-12-8-4-2-6-10(12)13(16)17/h1-8,15H,(H,16,17)

Names & synonyms

2-[(2-hydroxybenzoyl)oxy]benzoic acidDisalcidsalsalatosalsalatum

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

Classification & relationships

ChEBI ontology

Roles recorded in ChEBI

antiatherosclerotic agentnon-steroidal anti-inflammatory druganalgesicnon-narcotic analgesichypoglycemic agentantineoplastic agentEC 3.5.2.6 (beta-lactamase) inhibitorantirheumatic drugprodruginsulin-sensitizing drug

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

Mass ↔ amount of substance

Calculated from sourced mass
Equivalent amount
0.00387253 mol

Uses 258.229 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
65.12%
O
Oxygen · 5 atoms
30.98%
H
Hydrogen · 10 atoms
3.90%

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
Beta-lactamase inhibitory component from the roots of Fissistigma cavaleriei. ↗Phytomedicine : international journal of phytotherapy and phytopharmacology · 2010 Feb · PMID 19747808

Sources & record history

Checked 27 Sep 2026
EMBL-EBI ChEBI · CHEBI:9014

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

NCBI PubChem · CID 5161 · 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.