2,4,6-Trichlorophenol: Difference between revisions
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==Overview== | |||
'''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]],<ref>{{cite journal | author=Ogunniyi TAB, Oni PO, Juba A, Asaolu SO, and Kolawole DO | title=Disinfectants/antiseptics in the management of guinea worm ulcers in the rural areas | journal=Acta Tropica | volume=74 | issue=1 | pages=33–38(6) | date=2000-01-05 | doi=10.1016/S0001-706X(99)00057-1}}</ref> [[defoliant]], and [[preservative|glue preservative]].<ref name="msds">{{cite web | title=Safety data for 2,4,6-trichlorophenol | publisher=''[[University of Oxford]]'' | date=2005-09-05 | url=http://physchem.ox.ac.uk/MSDS/TR/2,4,6-trichlorophenol.html | accessdate=2007-11-16| archiveurl= http://web.archive.org/web/20071014083328/http://physchem.ox.ac.uk/MSDS/TR/2,4,6-trichlorophenol.html| archivedate= 14 October 2007 <!--DASHBot-->| deadurl= no}}</ref> 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]]. | '''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]],<ref>{{cite journal | author=Ogunniyi TAB, Oni PO, Juba A, Asaolu SO, and Kolawole DO | title=Disinfectants/antiseptics in the management of guinea worm ulcers in the rural areas | journal=Acta Tropica | volume=74 | issue=1 | pages=33–38(6) | date=2000-01-05 | doi=10.1016/S0001-706X(99)00057-1}}</ref> [[defoliant]], and [[preservative|glue preservative]].<ref name="msds">{{cite web | title=Safety data for 2,4,6-trichlorophenol | publisher=''[[University of Oxford]]'' | date=2005-09-05 | url=http://physchem.ox.ac.uk/MSDS/TR/2,4,6-trichlorophenol.html | accessdate=2007-11-16| archiveurl= http://web.archive.org/web/20071014083328/http://physchem.ox.ac.uk/MSDS/TR/2,4,6-trichlorophenol.html| archivedate= 14 October 2007 <!--DASHBot-->| deadurl= no}}</ref> 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]]. | ||
Latest revision as of 04:29, 24 July 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]
Overview
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.
Health effects
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]
Environmental effects
2,4,6-Trichlorophenol is an environmental pollutant that has been found in fresh water lakes such as the Great Lakes.[6]
See also
- Trichlorophenol (for other isomers).
References
- ↑ Ogunniyi TAB, Oni PO, Juba A, Asaolu SO, and Kolawole DO (2000-01-05). "Disinfectants/antiseptics in the management of guinea worm ulcers in the rural areas". Acta Tropica. 74 (1): 33–38(6). doi:10.1016/S0001-706X(99)00057-1.
- ↑ "Safety data for 2,4,6-trichlorophenol". University of Oxford. 2005-09-05. Archived from the original on 14 October 2007. Retrieved 2007-11-16.
- ↑ "2,4,6-Trichlorophenol". The Carcinogenic Potency Database Project, University of Berkeley. 2007-10-03. Archived from the original on 4 December 2007. Retrieved 2007-11-16.
- ↑ 4.0 4.1 "2,4,6 Trichlorophenol". United States Environmental Protection Agency. 2000. Retrieved 2007-11-16. Unknown parameter
|month=ignored (help) - ↑ "2,4,6-Trichlorophenol". ICSC 1122. IPCS. 1998. Retrieved 2007-11-16. Unknown parameter
|month=ignored (help) - ↑ TP Halappa Gowdal, John D Lock, and Ruth G Kurtz (1985). "A comprehensive study of risk assessment for a hazardous compound of public health concern". Water Air and Soil Pollution. 24 (2). doi:10.1007/BF00285444. Retrieved 2007-11-16. Unknown parameter
|month=ignored (help)
External links
de:2,4,6-Trichlorphenol fa:۲،۴،۶-تریکلروفنول uk:2,4,6-Трихлорфенол