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2,4,6-Trichlorophenol

2,4,6-Trichlorophenol
Chemical structure of 2,4,6-trichlorophenol
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2,4,6-Trichlorophenol.jpg
Names
IUPAC name
2,4,6-Trichlorophenol
Identifiers
3D model (Jmol)
ChEBI
ChemSpider
ECHA InfoCard 100.001.633
EC Number 604-018-00-5
RTECS number SN1575000
UN number 2020
Properties
C6H2Cl3OH/C6H3Cl3O
Molar mass 197.45 g/mol
Appearance yellow-whitish lumps or powder
Density 1.675 g/cm3
Melting point 69 °C (156 °F; 342 K)
Boiling point 246 °C (475 °F; 519 K) at 28 torr
Hazards
R-phrases R22, R36, R38, R40, R50, R53
S-phrases (S2), S36, S37, S60, S61
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N  (what is YesYN ?)
Infobox references

2,4,6-Trichlorophenol, also known as TCP, phenaclor, Dowicide 2S, Dowcide 2S, omal, is a chlorinated phenol that has been used as a fungicide, herbicide, insecticide, antiseptic,defoliant, and glue preservative. It is a clear to yellowish crystalline solid with a strong, phenolic odor. It decomposes on heating to produce toxic and corrosive fumes including hydrogen chloride and chlorine.

In animal models, consumption of 2,4,6-trichlorophenol leads to an increased incidence of lymphomas, leukemia, and liver cancer. It is classified as Group B2 (probable human carcinogen) by the United States Environmental Protection Agency. The technical grade of this substance may contain polychlorinated dibenzodioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), and other contaminants.

2,4,6-Trichlorophenol is an environmental pollutant that has been found in fresh water lakes such as the Great Lakes.


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