Search results
Results From The WOW.Com Content Network
The earliest record of trichloroethylene synthesis dates back to 1836. It was obtained from the action of potassium hydroxide on 1,1,2,2-tetrachloroethane and 1,1,1,2-tetrachloroethane by Auguste Laurent and notated as C 4 HCl 3 (then the atomic weight of carbon was thought to be the half of it really was).
These solvents tend to be relatively non-polar; they are therefore immiscible with water and effective in cleaning applications such as degreasing and dry cleaning for their ability to dissolve oils and grease. They are mostly nonflammable or have very low flammability.
This page provides supplementary chemical data on trichloroethylene. Material Safety Data Sheet The handling of this chemical may incur notable safety precautions. ...
Trichloroethylene is a major byproduct, which is separated by distillation. Worldwide production was about 1 million metric tons (980,000 long tons; 1,100,000 short tons) in 1985. [11] Although in very small amounts, tetrachloroethylene occurs naturally in volcanoes along with trichloroethylene. [12]
It is a colourless, sweet-smelling liquid that does not dissolve in water, but is soluble in most organic solvents. It is an isomer of 1,1,1-trichloroethane, and a byproduct of its manufacture. It is used as a solvent and as an intermediate in the synthesis of 1,1-dichloroethylene. [4]
1,1,1-Trichloroethane is an excellent solvent for many organic compounds and also one of the least toxic of the chlorinated hydrocarbons.It is generally considered non-polar, but owing to the good polarizability of the chlorine atoms, it is a superior solvent for organic compounds that do not dissolve well in hydrocarbons such as hexane.
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.
Vinyl fluoride, vinylidene fluoride, tetrafluoroethylene, trichloroethylene Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references