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Molar mass: 119.37 g·mol −1 ... Chloroform, [10] or ... Chloroform "The Molecular Lifesaver" – An article at Oxford University providing facts about chloroform.
The handling of this chemical may incur notable safety precautions. It is highly recommend that you seek the Material Safety ... log 10 of Chloroform vapor pressure.
Most low molecular weight and liquid chlorinated hydrocarbons such as dichloromethane, chloroform, carbon tetrachloride, dichloroethylene, trichloroethylene, tetrachloroethylene, 1,2-Dichloroethane and hexachlorobutadiene are useful solvents.
Common trihalomethanes (ordered by molecular weight) Molecular formula IUPAC name CAS registry number Common name Other names Molecule CHF 3: trifluoromethane 75-46-7 fluoroform: Freon 23, R-23, HFC-23 CHClF 2: chlorodifluoromethane 75-45-6 chlorodifluoromethane: R-22, HCFC-22 CHCl 3: trichloromethane 67-66-3 chloroform: R-20, methyl ...
Molecular weight (M.W.) (for molecular compounds) and formula weight (F.W.) (for non-molecular compounds), are older terms for what is now more correctly called the relative molar mass (M r). [8] This is a dimensionless quantity (i.e., a pure number, without units) equal to the molar mass divided by the molar mass constant .
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]
The chemical compound's low boiling point allows the chemical to function in a heat engine that can extract mechanical energy from small temperature differences. An example of a DCM heat engine is the drinking bird. The toy works at room temperature. [17]
Deuterated chloroform, also known as chloroform-d, is the organic compound with the formula CDCl 3. Deuterated chloroform is a common solvent used in NMR spectroscopy. [2] The properties of CDCl 3 and ordinary CHCl 3 are virtually identical. Deuterochloroform was first made in 1935 during the years of research on deuterium. [3]