Crotonic acid ((2E)-but-2-enoic acid) is a short-chain unsaturatedcarboxylic acid described by the formula CH3CH=CHCO2H. The name crotonic acid was given because it was erroneously thought to be a saponification product of croton oil.[1] It crystallizes as colorless needles from hot water. With a cis-alkene, Isocrotonic acid is an isomer of crotonic acid. Crotonic acid is soluble in water and many organic solvents. Its odor is similar to that of butyric acid.
Crotonic acid crystallizes in the monoclinic crystal system in the space group P21/a (space group 14, position 3) with the lattice parametersa = 971 pm, b = 690 pm, c = 775 pm and β = 104.0°. The unit cell contains four formula units.[7]
Crotonic acid reacts with ammonia at the alpha position in the presence of mercury(II) acetate. This reaction provides [[threonine|Template:Sc-threonine]].[12]
Use
Crotonic acid is mainly used as a comonomer with vinyl acetate.[13] The resulting copolymers are used in paints and adhesives.[3]
Crotonyl chloride reacts with N-ethyl-2-methylaniline (N-ethyl-o-toluidine) to provide crotamiton, which is used as an agent against scabies.[14]