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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, [3] defoliant, and glue preservative. [4] It is a clear to yellowish crystalline solid with a strong, phenolic odor.
Trichlorophenols are produced by electrophilic halogenation of phenol with chlorine. [1] Different isomers of trichlorophenol exist according to which ring positions on the phenol contain chlorine atoms. 2,4,6-Trichlorophenol, for example, has two chlorine atoms in the ortho positions and one chlorine atom in the para position.
Chemical structure of 2-chlorophenol. A chlorophenol is any organochloride of phenol that contains one or more covalently bonded chlorine atoms. There are five basic types of chlorophenols (mono- to pentachlorophenol) and 19 different chlorophenols in total when positional isomerism is taken into account.
C 6 H 2 Cl 3 NO 2,6-Dichloroquinone-4-chloroimideGibbs reagent C 6 H 3 Br 3 O: 2,4,6-Tribromophenol: C 6 H 3 Cl 3 O: 2,4,6-Trichlorophenol: C 6 H 4 BrNO 2: 5-bromonicotinic acid: 20826-04-4 C 6 H 4 ClNO 2: 2-chloronicotinic acid: 2942-59-8 C 6 H 4 ClN 3: 4-Chlorophenyl azide: C 6 H 4 ClNO 2: 6-chloro-2-pyridinecarboxylic acid: 4684-94-0 6 ...
CAS Number. 58-90-2 3D model ... 2,3,4,6-Tetrachlorophenol (2,3,4,6-TCP) is a chlorinated derivative of phenol with the molecular formula C 6 H 2 Cl 4 O. References
TCPO, or bis(2,4,6-trichlorophenyl) oxalate, is a chemical used in some types of glow sticks and is a key chemical in many chemiluminescent reactions. TCPO is classified as damaging to human organs and toxic if inhaled with an inhalable toxicity of 3.02 mg/L and oral toxicity LD50 of 820 mg/kg (rat).
The human olfactometry threshold for TCA is 4–10 ng L−1 in white wine and 50 ng L−1 in red wine. In the case of wine, a worldwide loss of roughly US$1 billion per year is attributed to cork taint. Science Direct Staff (June 2023). "2-4-6-Trichloroanisole" (Science Direct citation sample/listing)
Tetrachlorophenols are produced by electrophilic halogenation of phenol with chlorine. [1] Different isomers of tetrachlorophenol exist according to which ring positions on the phenol contain chlorine atoms. There are three different isomers: 2,3,4,5-Tetrachlorophenol; 2,3,4,6-Tetrachlorophenol; 2,3,5,6-Tetrachlorophenol
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