Etanidazole
A monocarboxylic acid amide obtained by formal condensation of the carboxy group of (2-nitro-1H-imidazol-1-yl)acetic acid with the amino group of ethanolamine. Used as a radiosensitising agent for hypoxic tumour cells. — ChEBI
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Identity & molecular properties
Source-linked values| CAS number | 22668-01-5 | ChEBI ↗ |
| Molecular formula | C7H10N4O4 | ChEBI ↗ |
| Molar mass | 214.181 g/mol | ChEBI ↗ |
| Monoisotopic mass | 214.0702 Da | ChEBI ↗ |
| Formal charge | 0 | ChEBI ↗ |
| ChEBI identifier | CHEBI:75473 | ChEBI ↗ |
Cross-source molecular data
PubChem| Molar mass | 214.18 g/mol | PubChem ↗ |
| Exact mass | 214.07020481 Da | PubChem ↗ |
| Computed XLogP | -1.3 | PubChem ↗ |
| Topological polar surface area (Ų) | 113 | PubChem ↗ |
| H-bond donors | 2 | PubChem ↗ |
| H-bond acceptors | 5 | PubChem ↗ |
| Rotatable bonds | 4 | PubChem ↗ |
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 identifieretanidazoleN-(2-hydroxyethyl)-2-(2-nitro-1H-imidazol-1-yl)acetamideWCDWBPCFGJXFJZ-UHFFFAOYSA-NO=C(Cn1ccnc1[N+](=O)[O-])NCCOInChI=1S/C7H10N4O4/c12-4-2-8-6(13)5-10-3-1-9-7(10)11(14)15/h1,3,12H,2,4-5H2,(H,8,13)Names & synonyms
Names are supplied by ChEBI. Trade names and related synonyms may describe a broader product context.
Classification & relationships
ChEBI ontologyRoles recorded in ChEBI
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 massUses 214.181 g/mol from ChEBI. Assumes the substance described by this record; no purity or concentration correction is applied.
Elemental composition
Theoretical mass fractionsCONHCalculated 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 associationsSources & record history
Checked 27 Sep 2026Release 255, 9 September 2026. ChEBI three-star (manually annotated) source entry. View original record ↗ · CC BY 4.0
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.