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triclosan

Structure via PubChem · Public domain (PubChem)

EntityQ408646· pop 34· linked from 793 articles

Also known as Stri-Dex Cleansing Bar, CH-3565, DNDI1246774, Stri-Dex Face Wash, 2,4,4'-Trichloro-2'-hydroxydiphenyl ether, 5-Chloro-2-(2,4-dichloro-phenoxy)-phenol, Triclosanum

Triclosan (sometimes abbreviated as TCS) is an antibacterial and antifungal agent present in some consumer products, including toothpaste, soaps, detergents, toys, and surgical cleaning treatments. It is similar in its uses and mechanism of action to triclocarban. Its efficacy as an antimicrobial agent, the risk of antimicrobial resistance, and its possible role in disrupted hormonal development remains controversial. Additional research seeks to understand its potential effects on organisms and environmental health.

Chemical data

Formula
C12H7Cl3O2
Molecular weight
289.5 g/mol
IUPAC name
5-chloro-2-(2,4-dichlorophenoxy)phenol
SMILES
C1=CC(=C(C=C1Cl)O)OC2=C(C=C(C=C2)Cl)Cl
InChIKey
XEFQLINVKFYRCS-UHFFFAOYSA-N
XLogP
5
Polar surface area
29.5 Ų
H-bond donors
1
H-bond acceptors
2
Formal charge
0

via PubChem

Research

5,652 papers

via PubMed

Wikidata facts

Mass
287.951
Has use
medication
Show 6 more facts
chemical formula
C₁₂H₇Cl₃O₂
canonical SMILES
C1=CC(=C(C=C1Cl)O)OC2=C(C=C(C=C2)Cl)Cl
World Health Organisation international non-proprietary name
triclosan
melting point
57
MCN code
2909.50.11
Commons category
Triclosan
Sources (3)

via Wikidata · CC0

~24 min read

Encyclopedic overview

23 sections
Contents
  • Uses
  • Effectiveness
  • Chemical structure and properties
  • Synthesis
  • Mechanism of action
  • Endocrine disruptor
  • Efflux pump inducer
  • Exposure
  • Distribution, metabolism, and elimination
  • Health concerns
  • Allergic
  • By-product exposure
  • Hormonal
  • History
  • Environmental concerns
  • Treatment and disposal
  • Bioaccumulation
  • Ecotoxicity
  • Resistance concerns
  • Alternatives
  • Policy
  • See also
  • References

Triclosan (sometimes abbreviated as TCS) is an antibacterial and antifungal agent present in some consumer products, including toothpaste, soaps, detergents, toys, and surgical cleaning treatments. It is similar in its uses and mechanism of action to triclocarban. Its efficacy as an antimicrobial agent, the risk of antimicrobial resistance, and its possible role in disrupted hormonal development remains controversial. Additional research seeks to understand its potential effects on organisms and environmental health.

Triclosan was developed in 1966. A 2006 study recommended showering with 2% triclosan as a regimen in surgical units to rid patients' skin of methicillin-resistant Staphylococcus aureus (MRSA). == Uses == Triclosan was used as a hospital scrub in the 1970s. Prior to its change in regulatory status in the EU and US, it had expanded commercially and was a common ingredient in soaps (0.10–1.00%), shampoos, deodorants, toothpastes, mouthwashes, cleaning supplies, and pesticides. It also was part of consumer products, including kitchen utensils, toys, bedding, socks, and trash bags.

Excerpted from Wikipedia’s “triclosan” article, available under the CC BY-SA 4.0 licence.