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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.
The EPA limits the total concentration of the four chief constituents (chloroform, bromoform, bromodichloromethane, and dibromochloromethane), referred to as total trihalomethanes (TTHM), to 80 parts per billion in treated water. [6] Traces of chloroform are produced in swimming pools. [7] [8] [9] [10]
Like all macroalgae, Asparagopsis contains bromoform, a halogen compound which is known to inhibit methane production in ruminants. It has been shown to convert much of the enteric methane (a powerful greenhouse gas) to energy (and some carbon dioxide) for cattle during normal digestion. Because of its high bromoform content, Asparagopsis has ...
While dichloromethane extract was the most potent bioactive, reducing methane production by 79%, bromoform and dibromochloromethane had the highest activity inhibiting methane production, and only bromoform is present in sufficient quantities to be effective. [12]
Representative agents include bromoform and dibromodimethylhydantoin ("DBDMH"). [7] Some herbicides, such as bromoxynil , contain also bromine moieties. Like other halogenated pesticides , bromoxynil is subject to reductive dehalogenation under anaerobic conditions, and can be debrominated by organisms originally isolated for their ability to ...
One of the most important uses of the Sandmeyer reaction is the formation of aryl halides. The solvent of choice for the synthesis of iodoarenes is diiodomethane, [17] [18] while for the synthesis of bromoarenes, bromoform is used. For the synthesis of chloroarenes, chloroform is the solvent of choice. [19]
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.
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