Methacrylic acid

This colorless, viscous liquid is a carboxylic acid with an acrid unpleasant odor.

Another route to methacrylic acid starts with isobutylene, which obtainable by dehydration of tert-butanol.

[8] MAA occurs naturally in small amounts in the oil of Roman chamomile.

For commercial applications, MAA is polymerized using azobisisobutyronitrile as a thermally activated free-radical catalyst.

Esterifications are brought about by acid-catalyzed condensations with alcohols, alkylations with certain alkenes, and transesterifications.

Structural formula of methacrylic acid
Ball-and-stick model of the methacrylic acid molecule
NFPA 704 four-colored diamond Health 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gas Flammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuel 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 hazards (white): no code
Typical vinyl ester resin derived from bisphenol A diglycidyl ether and methacrylic acid. [ 9 ]