caprylic acid

chemical compound
Also known as: octanoic acid

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carboxylic acids

  • oxidation of alcohols
    In carboxylic acid: Saturated aliphatic acids

    …and 10-carbon acids: hexanoic (caproic), octanoic (caprylic), and decanoic (capric) acids, respectively. Common names for these three acids are derived from the Latin caper, meaning “goat.” Some hard cheeses (e.g., Swiss cheese) contain natural propanoic acid. The higher even-numbered saturated acids, from C12 to C18 (lauric, myristic,

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Also called:
ethanoic acid

acetic acid (CH3COOH), the most important of the carboxylic acids. A dilute (approximately 5 percent by volume) solution of acetic acid produced by fermentation and oxidation of natural carbohydrates is called vinegar; a salt, ester, or acylal of acetic acid is called acetate. Industrially, acetic acid is used in the preparation of metal acetates, used in some printing processes; vinyl acetate, employed in the production of plastics; cellulose acetate, used in making photographic films and textiles; and volatile organic esters (such as ethyl and butyl acetates), widely used as solvents for resins, paints, and lacquers. Biologically, acetic acid is an important metabolic intermediate, and it occurs naturally in body fluids and in plant juices.

Acetic acid has been prepared on an industrial scale by air oxidation of acetaldehyde, by oxidation of ethanol (ethyl alcohol), and by oxidation of butane and butene. Today acetic acid is manufactured by a process developed by the chemical company Monsanto in the 1960s; it involves a rhodium-iodine catalyzed carbonylation of methanol (methyl alcohol).

Synthesis of acetic acid from methanol and carbon monoxide. chemical compound

Pure acetic acid, often called glacial acetic acid, is a corrosive, colourless liquid (boiling point 117.9 °C [244.2 °F]; melting point 16.6 °C [61.9 °F]) that is completely miscible with water.

William H. Brown
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