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  2. Dichloromethane - Wikipedia

    en.wikipedia.org/wiki/Dichloromethane

    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 .

  3. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    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. [2]

  4. Dichloromethane (data page) - Wikipedia

    en.wikipedia.org/wiki/Dichloromethane_(data_page)

    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 ...

  5. Solvent - Wikipedia

    en.wikipedia.org/wiki/Solvent

    Small amounts of low-boiling-point solvents like diethyl ether, dichloromethane, or acetone will evaporate in seconds at room temperature, while high-boiling-point solvents like water or dimethyl sulfoxide need higher temperatures, an air flow, or the application of vacuum for fast evaporation.

  6. Dihalomethane - Wikipedia

    en.wikipedia.org/wiki/Dihalomethane

    There are four members with only one kind of halogen atom: difluoromethane, dichloromethane, dibromomethane and diiodomethane. Structural Formula: Name Difluoromethane:

  7. 1,1-Dichloroethane - Wikipedia

    en.wikipedia.org/wiki/1,1-Dichloroethane

    1,1-Dichloroethane is a chlorinated hydrocarbon.It is a colorless oily liquid with a chloroform-like odor.It is not easily soluble in water, but miscible with most organic solvents.

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  9. Carbon tetrachloride - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrachloride

    Hydrogen or an acid in the presence of an iron catalyst can reduce carbon tetrachloride to chloroform, dichloromethane, chloromethane and even methane. [9] When its vapours are passed through a red-hot tube, carbon tetrachloride dechlorinates to tetrachloroethylene and hexachloroethane .

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