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

Oxatomide

60607-34-3C27H30N4O426.564 g/mol

A member of the class of benzimidazoles that is 1,3-dihydro-2H-benzimidazol-2-one substituted by a 3-[4-(diphenylmethyl)piperazin-1-yl]propyl group at position 1. It is an anti-allergic drug. — ChEBI

Safety references

Safety documents & references

Supplier matching matters

Find the safety document for your specific supplier, product number and grade.

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 number60607-34-3ChEBI ↗
Molecular formulaC27H30N4OChEBI ↗
Molar mass426.564 g/molChEBI ↗
Monoisotopic mass426.24196 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:31943ChEBI ↗

Cross-source molecular data

PubChem
Molar mass426.6 g/molPubChem ↗
Exact mass426.24196159 DaPubChem ↗
Computed XLogP4.1PubChem ↗
Topological polar surface area (Ų)38.8PubChem ↗
H-bond donors1PubChem ↗
H-bond acceptors3PubChem ↗
Rotatable bonds7PubChem ↗

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
oxatomide
1-{3-[4-(diphenylmethyl)piperazin-1-yl]propyl}-1,3-dihydro-2H-benzimidazol-2-one
BAINIUMDFURPJM-UHFFFAOYSA-N
O=c1nc2ccccc2n1CCCN1CCN(C(c2ccccc2)c2ccccc2)CC1
InChI=1S/C27H30N4O/c32-27-28-24-14-7-8-15-25(24)31(27)17-9-16-29-18-20-30(21-19-29)26(22-10-3-1-4-11-22)23-12-5-2-6-13-23/h1-8,10-15,26H,9,16-21H2,(H,28,32)

Names & synonyms

1-{3-[4-(diphenylmethyl)piperazin-1-yl]propyl}-1,3-dihydro-2H-benzimidazol-2-oneCeltectCeltomideCenacertCobionaoxatomidaoxatomidumTinset

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

Classification & relationships

ChEBI ontology

Roles recorded in ChEBI

geroprotectorH1-receptor antagonistserotonergic antagonistanti-allergic agentanti-inflammatory agent

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
0.00234431 mol

Uses 426.564 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 · 27 atoms
76.03%
N
Nitrogen · 4 atoms
13.13%
H
Hydrogen · 30 atoms
7.09%
O
Oxygen · 1 atom
3.75%

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
Antiinflammatory effects of oxatomide. ↗Journal of investigational allergology & clinical immunology · 1999 Jul-Aug · PMID 10513346
Drug eruption and liver injury caused by terfenadine and oxatomide. ↗European journal of dermatology : EJD · 2002 Jul-Aug · PMID 12095890
WO9858924 · 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:31943

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

NCBI PubChem · CID 4615 · 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.