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  2. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    About 6.7 million tonnes were produced worldwide in 2010, mainly for use as a solvent and for production of methyl methacrylate and bisphenol A, which are precursors to widely used plastics. [23] [24] It is a common building block in organic chemistry. It serves as a solvent in household products such as nail polish remover and paint thinner.

  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. DEA list of chemicals - Wikipedia

    en.wikipedia.org/wiki/DEA_list_of_chemicals

    It also maintains List I of chemicals and List II of chemicals, which contain chemicals that are used to manufacture the controlled substances/illicit drugs. The list is designated within the Controlled Substances Act [ 1 ] but can be modified by the U.S. Attorney General as illegal manufacturing practices change.

  5. Clostridium acetobutylicum - Wikipedia

    en.wikipedia.org/wiki/Clostridium_acetobutylicum

    Acetone was used in the important wartime task of casting cordite. The alcohols were used to produce vehicle fuels and synthetic rubber . Unlike yeast , which can digest only some sugars into alcohol and carbon dioxide , C. acetobutylicum and other Clostridia can digest whey , sugar, starch , cellulose and perhaps certain types of lignin ...

  6. Acetone peroxide - Wikipedia

    en.wikipedia.org/wiki/Acetone_peroxide

    The product made by using hydrochloric acid is regarded as more stable than the one made using sulfuric acid. It is known that traces of sulfuric acid trapped inside the formed acetone peroxide crystals lead to instability. In fact, the trapped sulfuric acid can induce detonation at temperatures as low as 50 °C (122 °F).

  7. Acetonide - Wikipedia

    en.wikipedia.org/wiki/Acetonide

    General structure of a 1,2-acetonide. The diol is shown in blue, the acetone part in red. In organic chemistry, an acetonide is the functional group composed of the cyclic ketal of a diol with acetone. The more systematic name for this structure is an isopropylidene ketal. Acetonide is a common protecting group for 1,2- and 1,3-diols. [1]

  8. Intel shapes Licking County's 10 biggest development stories ...

    www.aol.com/intel-shapes-licking-countys-10...

    The Intel Corporation's January 2022 announcement of its plans to build a $20 billion computer chip manufacturing operation just south of Johnstown was clearly the top story of 2022 in Licking ...

  9. Acetone–butanol–ethanol fermentation - Wikipedia

    en.wikipedia.org/wiki/Acetone–butanol–ethanol...

    The use of side products such as hydrogen and carbon dioxide, solid wastes and discharged microorganisms and carry out less expensive process wastewater treatments. In the second half of the 20th century, these technologies allowed an increase in the final product concentration in the broth from 15 to 30 g/L, an increase in the final ...