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  2. 2,4,6-Trichlorophenol - Wikipedia

    en.wikipedia.org/wiki/2,4,6-Trichlorophenol

    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.

  3. Trichlorophenol - Wikipedia

    en.wikipedia.org/wiki/Trichlorophenol

    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. There are six ...

  4. Chlorophenol - Wikipedia

    en.wikipedia.org/wiki/Chlorophenol

    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.

  5. Category:Phenols - Wikipedia

    en.wikipedia.org/wiki/Category:Phenols

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  6. TCPO - Wikipedia

    en.wikipedia.org/wiki/TCPO

    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).

  7. Tetrachlorophenol - Wikipedia

    en.wikipedia.org/wiki/Tetrachlorophenol

    A tetrachlorophenol is any organochloride of phenol that contains four covalently bonded chlorine atoms. 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:

  8. 2,4,6-Trichloroanisole - Wikipedia

    en.wikipedia.org/wiki/2,4,6-trichloroanisole

    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)

  9. 2,4,5-Trichlorophenol - Wikipedia

    en.wikipedia.org/wiki/2,4,5-Trichlorophenol

    2,4,5-Trichlorophenol (TCP) is an organochloride with the molecular formula C 6 H 3 Cl 3 O.It has been used as a fungicide and herbicide. [2] Precursor chemical used in the production of 2,4,5-Trichlorophenoxyacetic acid (2,4,5-T) and hexachlorophene involves the intermediate production of 2,4,5-trichlorophenol (TCP) and the formation of 2,3,7,8-Tetrachlorodibenzodioxin (TCDD, commonly ...