Triclosan is a widely used ingredient in cosmetics, personal care, and skincare formulations. Depending on its function, it may serve as a moisturizer, preservative, emulsifier, or active ingredient to enhance the overall effectiveness and performance of a product.
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.
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Names | |||
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Preferred IUPAC name
5-Chloro-2-(2,4-dichlorophenoxy)phenol | |||
Other names
2,4,4′-Trichloro-2′-hydroxydiphenyl ether
5-Chloro-(2,4-dichlorophenoxy)phenol Trichloro-2′-hydroxydiphenyl ether CH-3565 Lexol 300 Irgasan DP 300 Ster-Zac | |||
Identifiers | |||
3D model (JSmol)
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ChEBI | |||
ChEMBL | |||
ChemSpider | |||
DrugBank | |||
ECHA InfoCard | 100.020.167 | ||
KEGG | |||
PubChem CID
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UNII | |||
CompTox Dashboard (EPA)
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Properties | |||
C12H7Cl3O2 | |||
Molar mass | 289.54 g·mol−1 | ||
Appearance | White solid | ||
Density | 1.49 g/cm3 | ||
Melting point | 55–57 °C (131–135 °F; 328–330 K) | ||
Boiling point | 120 °C (248 °F; 393 K) | ||
Pharmacology | |||
D08AE04 (WHO) D09AA06 (WHO) (medicated dressing) | |||
Hazards | |||
NFPA 704 (fire diamond) | |||
Flash point | 162.2 °C (324.0 °F; 435.3 K) | ||
Safety data sheet (SDS) | MSDS | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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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).