2,4,6-Trichlorophenol | |
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2,4,6-Trichlorophenol |
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Identifiers | |
CAS number | 88-06-2 |
ChemSpider | 6648 |
EC number | 604-018-00-5 |
UN number | 2020 |
RTECS number | SN1575000 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C6H2Cl3OH/C6H3Cl3O |
Molar mass | 197.45 g/mol |
Density | 1.675 g/cm3 |
Melting point |
69 °C |
Boiling point |
246 °C at 28 torr |
Hazards | |
R-phrases | R22, R36, R38, R40, R50, R53 |
S-phrases | (S2), S36, S37, S60, S61 |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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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,[1] defoliant, and glue preservative.[2] It is a yellow solid with a strong, sweet odour. It decomposes on heating to produce toxic and corrosive fumes including hydrogen chloride and chlorine.
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2,4,6-Trichlorophenol is carcinogenic in animals, causing lymphomas, leukemia, and liver cancer via oral exposure.[3][4] It is classified as Group B2 (probable human carcinogen) by the United States Environmental Protection Agency.[4] The technical grade of this substance may contain polychlorinated dibenzodioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), and other contaminants.[5]
2,4,6-Trichlorophenol is an environmental pollutant that has been found in fresh water lakes such as the Great Lakes.[6]