Triclocarban

Triclocarban
Names
Preferred IUPAC name
N-(4-Chlorophenyl)-N′-(3,4-dichlorophenyl)urea
Other names
Trichlorocarbanilide, TCC, Solubacter, Vivilide
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.002.659
UNII
  • 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) Y
    Key: ICUTUKXCWQYESQ-UHFFFAOYSA-N Y
  • InChI=1/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)
    Key: ICUTUKXCWQYESQ-UHFFFAOYAL
  • Clc2ccc(NC(=O)Nc1ccc(Cl)cc1)cc2Cl
Properties
C13H9Cl3N2O
Molar mass 315.58 g·mol−1
Density 1.53 g/cm3
Melting point 254 to 256 °C (489 to 493 °F; 527 to 529 K)
Hazards
NFPA 704 (fire diamond)
0
1
0
Flash point > 150 °C (302 °F; 423 K)
Lethal dose or concentration (LD, LC):
>5000 mg/kg (oral, mouse)
2100 mg/kg (i.p., mouse)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Triclocarban (sometimes abbreviated as TCC) is an antibacterial chemical once common in, but now phased out of, personal care products like soaps and lotions. It was originally developed for the medical field. Although the mode of action is unknown, TCC can be effective in fighting infections by targeting the growth of bacteria such as Staphylococcus aureus. Additional research seeks to understand its potential for causing antibacterial resistance and its effects on organismal and environmental health.