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  2. Trihalomethane - Wikipedia

    en.wikipedia.org/wiki/Trihalomethane

    Trihalomethanes were the subject of the first drinking water regulations issued after passage of the U.S. Safe Drinking Water Act in 1974. [ 5 ] The EPA limits the total concentration of the four chief constituents ( chloroform , bromoform , bromodichloromethane , and dibromochloromethane ), referred to as total trihalomethanes (TTHM), to 80 ...

  3. Chloroform - Wikipedia

    en.wikipedia.org/wiki/Chloroform

    The chloroform molecule can be viewed as a methane molecule with three hydrogen atoms replaced with three chlorine atoms, leaving a single hydrogen atom. The name "chloroform" is a portmanteau of terchloride (tertiary chloride, a trichloride) and formyle, an obsolete name for the methylylidene radical (CH) derived from formic acid. [citation ...

  4. Disinfection by-product - Wikipedia

    en.wikipedia.org/wiki/Disinfection_by-product

    Swimming pools using chlorine have been found to contain trihalomethanes, although generally they are below current EU standard for drinking water (100 micrograms per litre). [4] Concentrations of trihalomethanes (mainly chloroform) of up to 0.43 ppm have been measured. [5]

  5. Trihalide - Wikipedia

    en.wikipedia.org/wiki/Trihalide

    The molecular structure of chloroform, one of the simplest trihalides. A trihalide in chemistry is an organohalide consisting of three halide atoms bonded to a single atom or compound. [1] [2] An example of a trihalide is chloroform. The trihalomethanes are the simplest trihalides, because only one hydrogen is connected to the

  6. 1,1,1-Trichloroethane - Wikipedia

    en.wikipedia.org/wiki/1,1,1-Trichloroethane

    The organic compound 1,1,1-trichloroethane, also known as methyl chloroform and chlorothene, is a chloroalkane with the chemical formula CH 3 CCl 3. It is an isomer of 1,1,2-trichloroethane . A colourless and sweet-smelling liquid, it was once produced industrially in large quantities for use as a solvent . [ 5 ]

  7. Haloform reaction - Wikipedia

    en.wikipedia.org/wiki/Haloform_reaction

    In chemistry, the haloform reaction (also referred to as the Lieben haloform reaction) is a chemical reaction in which a haloform (CHX 3, where X is a halogen) is produced by the exhaustive halogenation of an acetyl group (R−C(=O)CH 3, where R can be either a hydrogen atom, an alkyl or an aryl group), in the presence of a base.

  8. Bromoform - Wikipedia

    en.wikipedia.org/wiki/Bromoform

    Bromoform was discovered in 1832 by Löwig who distilled a mixture of bromal and potassium hydroxide, as analogous to preparation of chloroform from chloral. [5]Bromoform can be prepared by the haloform reaction using acetone and sodium hypobromite, by the electrolysis of potassium bromide in ethanol, or by treating chloroform with aluminium bromide.

  9. Bromodichloromethane - Wikipedia

    en.wikipedia.org/wiki/Bromodichloromethane

    Bromodichloromethane is a trihalomethane with formula C H Br Cl 2.It is a colorless, nonflammable liquid which will dissolve in water, or evaporate in air. [1] Most of the chemical is produced through the chlorine disinfection process, [1] and as a result it can occur in municipally-treated drinking water. [2]