triclocarban
A member of the class of phenylureas that is urea substituted by a 4-chlorophenyl group and a 3,4-dichlorophenyl group at positions 1 and 3 respectively.
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
Classification
Chemical structure
| Molecular formula | C13H9Cl3N2O |
|---|---|
| Charge | 0 |
| Average mass | 315.587 Da |
| Monoisotopic mass | 313.97805 Da |
| Source | ChEBI |
| InChIKey | ICUTUKXCWQYESQ-UHFFFAOYSA-N |
O=C(Nc1ccc(Cl)cc1)Nc1ccc(Cl)c(Cl)c1
InChI=1S/C13H9Cl3N2O/c14-8-1-3-9(4-2-8)17-13(19)18-10-5-6-11(15)12(16)7-10/h1-7H,(H2,17,18,19)
Also called
- Cutisan
- Nobacter
- Solubacter
- triclocarbanum
- 1-(4-chlorophenyl)-3-(3,4-dichlorophenyl)urea
- 1-(3',4'-dichlorophenyl)-3-(4'-chlorophenyl)urea
- 3,4,4'-trichloro carbanilide
- 3,4,4'-trichlorocarbanilide
- 3,4,4'-trichlorodiphenylurea
- N-(4-chlorophenyl)-N'-(3,4-dichlorophenyl)urea
- TCC
Cross-references
- cas:101-20-2
- reaxys:2814890
Drug registries
Patents and articles
Activity roles
- antimicrobial agent
CHEBI:33281 - disinfectant
CHEBI:48219
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:48347 |
triclocarban | antibioticmech:chebi-88b4af68dd |
2026-08-30 |
Curation history
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SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories