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1,1,2,2-Tetrabromoethane, or simply tetrabromoethane (TBE), is a halogenated hydrocarbon, chemical formula C 2 H 2 Br 4.Although three bromine atoms may bind to one of the carbon atoms creating 1,1,1,2-tetrabromoethane this is not thermodynamically favorable, so in practice tetrabromoethane is equal to 1,1,2,2-tetrabromoethane, where each carbon atom binds two bromine atoms.
Tribromoethylene is a bromoalkene and a trihaloethylene with the chemical formula C 2 HBr 3.It can be made from 1,1,2,2-tetrabromoethane. [3]Tribromoethylene reacts with potassium hydroxide to yield dibromoacetylene via dehydrobromination, [4] this reaction is analogous to the synthesis of dichloroacetylene from trichloroethylene.
These toxic chemicals are avoided today in consideration of the fact that there are alternative water based, non-toxic heavy liquids like sodium polytungstate solutions. [1] With this relatively new heavy liquid densities up to 3.1 g·cm −3 can be adjusted . Adding parts of pulverulent tungsten carbide increases the density to 4.6 g·cm −3. [2]
1,2-Dibromoethane; Tetrabromoethane; Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ...
Tetrabromoethane; 1,2,3-Tribromopropane This page was last edited on 2 December 2021, at 15:41 (UTC). Text is available under the Creative Commons Attribution ...
6.1: Tetrabromoethane: UN 2505: 6.1: Ammonium fluoride: UN 2506: 8: Ammonium hydrogen sulfate: ... Di-(3,5,5,-trimethyl-1,2-dioxolanyl-3)peroxide (UN No no longer in ...
1,1,2,2-tetrachloroethane was used in large amounts to produce other chemicals like trichloroethylene, tetrachloroethylene, and 1,2-dichloroethylene. [6] Because of its possible carcinogen effects on humans, the production of 1,1,2,2-tetrachloroethane has decreased significantly and is no longer widely used as an end-product. [7]
Tetrabromoethylene is a potential fungicide and bactericide on fruits. [1] It was used in mineral separation. [2] It is prepared from acetylene and bromine in multiple steps. [1] [3] One method involves dehydrobromination of pentabromoethane, other method involves bromination of dibromoethylene in chloroform. [1]