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    Acetone

    Acetone in Tradeasia

    IUPAC Name

    Propan-2-one

    Cas Number

    67-64-1

    HS Code

    2914.11.00

    Formula

    CH3COCH<

    Basic Info

    Appearance

    Clear, Colorless Liquid

    Common Names

    Propanone, Dimethyl Ketone

    Packaging

    100 @ 200 kg Iron Drum, 20 MT / 20FCL

    Brief Overview

    Acetone, also known as propanone, is a clear, colorless, flammable, and volatile liquid with a molecular formula of CH3COCH3. Due to its small size and the presence of the carbonyl group, acetone is capable to form favorable interactions with water. These properties cemented its position as an ideal solvent for cleaning purposes in the laboratory as it is miscible in both water and organic solvents.

    Small quantities of acetone can be found naturally in plants and animals as it is a metabolic product. Previous studies have explored the relationship between diabetes and acetone concentration in blood and urine which observes that diabetic patients tend to have larger amounts of acetone. Even though it is a natural product found in our bodies, acetone is toxic in high doses.

    Acetone is capable of dissolving plastic glasses frames, jewelry, pens and pencils, rayon stockings, and other rayon garments. Acetone can polymerize rapidly under the influence of air, light, or upon heating. It can also polymerize upon contact with a catalyst, strong oxidizers, and various metals such as copper and aluminum.

     

    Manufacturing Process

    Acetone can be obtained directly or indirectly from propene. Currently, the indirect oxidation of propene is the most preferred method which contributes to about 83% of acetone production. This process consists of two major steps with the first step involving the Friedel-Crafts alkylation of benzene with propene to produce cumene. The resulting cumene is oxidized to give cumene hydroperoxide (CHP). Using a strong mineral acid as a catalyst, CHP is cleaved to produce acetone and phenol.

    An alternative synthesis is the catalytic dehydrogenation of 2-propanol to acetone where 2-propanol is obtained from the hydration of propene. This synthesis route used to account for 50-60% of the acetone production in the USA during the 1970s but due to the lower costs of cumene oxidation, this methodology has declined ever since.

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