Acetyl chloride

It belongs to the class of organic compounds called acid halides.

However, these methods usually give acetyl chloride contaminated by phosphorus or sulfur impurities, which may interfere with the organic reactions.

For further information on the types of chemical reactions compounds such as acetyl chloride can undergo, see acyl halide.

Two major classes of acetylations include esterification and the Friedel-Crafts reaction.

Acetyl chloride is a reagent for the preparation of esters and amides of acetic acid, used in the derivatization of alcohols and amines.

Skeletal formula of acetyl chloride
Skeletal formula of acetyl chloride
Ball-and-stick model of acetyl chloride
Ball-and-stick model of acetyl chloride
Space-filling model of acetyl chloride
Space-filling model of acetyl chloride
NFPA 704 four-colored diamond Health 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gas Flammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasoline Instability 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g. white phosphorus Special hazard W: Reacts with water in an unusual or dangerous manner. E.g. sodium, sulfuric acid