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  2. Dimethyl carbonate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_carbonate

    DMC is still safer than acetone, methyl acetate and methyl ethyl ketone from a flammability point of view. The National Center for Sustainable Transportation recommends limiting exposure by inhalation to less than 100 ppm over an 8-hour work day, which is similar to that of a number of common industrial solvents (toluene, methyl ethyl ketone). [20]

  3. VOC exempt solvent - Wikipedia

    en.wikipedia.org/wiki/VOC_exempt_solvent

    Due to its classification as VOC exempt, dimethyl carbonate has grown in popularity and applications as a replacement for methyl ethyl ketone (MEK) and other solvents. tert-Butyl acetate is used as a solvent in the production of lacquers, enamels, inks, adhesives, thinners and industrial cleaners. [10] [11] It also gained EPA VOC exempt status.

  4. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    The derived names of ketones are obtained by writing separately the names of the two alkyl groups attached to the carbonyl group, followed by "ketone" as a separate word. Traditionally the names of the alkyl groups were written in order of increasing complexity, for example methyl ethyl ketone .

  5. Butanone - Wikipedia

    en.wikipedia.org/wiki/Butanone

    Butanone, also known as methyl ethyl ketone (MEK) or ethyl methyl ketone, [a] is an organic compound with the formula CH 3 C(O)CH 2 CH 3. This colorless liquid ketone has a sharp, sweet odor reminiscent of acetone. It is produced industrially on a large scale, but occurs in nature only in trace amounts. [7]

  6. 2-Pentanone - Wikipedia

    en.wikipedia.org/wiki/2-pentanone

    2-Pentanone or methyl propyl ketone (MPK) is a ketone and solvent of minor importance. It is comparable to methyl ethyl ketone , but has a lower solvency and is more expensive. [ 5 ] It occurs naturally in Nicotiana tabacum (Tobacco) [ 6 ] and blue cheese as a metabolic product of Penicillium mold growth.

  7. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    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.

  8. Ozonolysis - Wikipedia

    en.wikipedia.org/wiki/Ozonolysis

    Next, the molozonide reverts to its corresponding carbonyl oxide (also called the Criegee intermediate or Criegee zwitterion) and aldehyde or ketone (3) in a retro-1,3-dipolar cycloaddition. The oxide and aldehyde or ketone react again in a 1,3-dipolar cycloaddition, producing a relatively stable ozonide intermediate, known as a trioxolane (4).

  9. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    Methyl ethyl ketone peroxide, benzoyl peroxide and to a smaller degree acetone peroxide are used as initiators for radical polymerization of some thermosets, e.g. unsaturated polyester and vinyl ester resins, often encountered when making fiberglass or carbon fiber composites (CFRP), with examples including boats, RV units, bath tubs, pools ...