• reaction
  • Triclocarban is incompatible with strong oxidizing reagents and strong bases, reaction with which could result in safety concerns such as explosion, toxicity, gas, and heat. (wikipedia.org)
  • There are two commercial routes used for the production of triclocarban, using the reaction of isocyanates with nucleophiles such as amines to form ureas: 4-chlorophenylisocyanate is reacted with 3,4-dichloroaniline 3,4-dichlorophenylisocyanate is reacted with 4-chloroaniline The purity specification in the draft USP monograph for triclocarban is: not less than 97.0% w/w. (wikipedia.org)
  • It can be used industrially in the preparation of triclocarban by reaction with p-chloroaniline. (wikipedia.org)
  • DRUG
  • In December 2013, the Food and Drug Administration required all companies to prove within the next year, that triclocarban is not harmful to consumers. (wikipedia.org)
  • skin
  • Triclocarban acts to effectively treat both initial bacterial skin and mucosal infections as well as those infections at risk for superinfection. (wikipedia.org)