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Chemical substance record

Oxolinic acid

14698-29-4C13H11NO5261.233 g/mol

A quinolinemonocarboxylic acid having the carboxy group at position 7 as well as oxo and ethyl groups at positions 4 and 1 respectively and a dioxolo ring fused at the 5- and 6-positions. A synthetic antibiotic, it is used in veterinary medicine for the treatment of bacterial infections in cattle, pigs and poultry. — ChEBI

Safety references

Safety documents & references

1 indexed references
JP · NITE

Government GHS classification

24A6030 · FY2012

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 number14698-29-4ChEBI ↗
Molecular formulaC13H11NO5ChEBI ↗
Molar mass261.233 g/molChEBI ↗
Monoisotopic mass261.06372 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:138856ChEBI ↗

Cross-source molecular data

PubChem
Molar mass261.23 g/molPubChem ↗
Exact mass261.06372245 DaPubChem ↗
Computed XLogP-0.2PubChem ↗
Topological polar surface area (Ų)76.1PubChem ↗
H-bond donors1PubChem ↗
H-bond acceptors6PubChem ↗
Rotatable bonds2PubChem ↗

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
oxolinic acid
5-ethyl-8-oxo-5,8-dihydro[1,3]dioxolo[4,5-g]quinoline-7-carboxylic acid
KYGZCKSPAKDVKC-UHFFFAOYSA-N
CCn1cc(C(=O)O)c(=O)c2cc3c(cc21)OCO3
InChI=1S/C13H11NO5/c1-2-14-5-8(13(16)17)12(15)7-3-10-11(4-9(7)14)19-6-18-10/h3-5H,2,6H2,1H3,(H,16,17)

Names & synonyms

5-ethyl-8-oxo-5,8-dihydro[1,3]dioxolo[4,5-g]quinoline-7-carboxylic acidacide oxoliniqueacido oxolinicoacidum oxolinicum

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

Classification & relationships

ChEBI ontology

Roles recorded in ChEBI

enzyme inhibitorantimicrobial agentantibacterial agentantiinfective agentantifungal agentantibacterial drug

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 · FY2012 source classification
Oxolinic acid · 24A6030
EndpointReported classification
Acute toxicity (Inhalation: Dusts and mists)Category 4
Specific target organ toxicity - Single exposureCategory 2 (central nervous system)
Specific target organ toxicity - Repeated exposureCategory 2 (nervous system)
Hazardous to the aquatic environment (Acute)Category 2
Hazardous to the aquatic environment (Long-term)Category 2

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
0.003828 mol

Uses 261.233 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 · 13 atoms
59.77%
O
Oxygen · 5 atoms
30.62%
N
Nitrogen · 1 atom
5.36%
H
Hydrogen · 11 atoms
4.24%

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
Pharmacokinetics of nalidixinic acid and oxolinic acid in healthy women. ↗Clinical pharmacology and therapeutics · 1976 Jan · PMID 1245092
US3287458 · 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:138856

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

NCBI PubChem · CID 4628 · 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.