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Dichloromethane (DCM, methylene chloride, or methylene bichloride) is an organochlorine compound with the formula C H 2 Cl 2. This colorless, volatile liquid with a chloroform-like, sweet odor is widely used as a solvent. Although it is not miscible with water, it is slightly polar, and miscible with many organic solvents. [12]
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
The most important is dichloromethane, which is mainly used as a solvent. Chloromethane is a precursor to chlorosilanes and silicones . Historically significant (as an anaesthetic), but smaller in scale is chloroform, mainly a precursor to chlorodifluoromethane (CHClF 2 ) and tetrafluoroethene which is used in the manufacture of Teflon.
log 10 of Dichloromethane vapor pressure. Uses formula: log e P m m H g = {\displaystyle \scriptstyle \log _{e}P_{mmHg}=} log e ( 760 101.325 ) − 10.08632 log e ( T + 273.15 ) − 6030.610 T + 273.15 + 80.87786 + 9.812512 × 10 − 6 ( T + 273.15 ) 2 {\displaystyle \scriptstyle \log _{e}({\frac {760}{101.325}})-10.08632\log _{e ...
The hydrocarbons used are sometimes made by hydrogenation from naphtha. The lipophilic liquids dissolve fat-soluble lubricants or oils. Some products also contain polar solvents such as ethanol, [7] methanol, [8] isopropanol, and acetone in order to dissolve non-lipophilic substances. Many formulations are incompatible with various materials ...
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 ...
The remaining water is treated with solvents (e.g. dichloromethane or ethyl acetate) to extract the caffeine from the water. As in other methods, the caffeine can then be separated from the organic solvent by simple evaporation. The same water is recycled through this two-step process with new batches of beans.
Aside from those few exceptions, free-radical halogenation is notoriously unselective. Chlorination rarely stops at monosubstitution: [2] depending on reaction conditions, methane chlorination yields varying proportions of chloromethane, dichloromethane, chloroform and carbon tetrachloride.
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