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The chirality of the title compound, C 19 H 26 O 2 , is solely generated by the presence of the double bond in the cyclo­hexene ring. This compound was synthesized to study the inter­action of the two enanti­omers in the solid state. The resultant racemate is made up of carboxylic acid  RS  dimers. Inter­molecular O—H⋯O hydrogen bonds produce centrosymmetric  R22 (8) rings which dimerize the two chiral enanti­omers through their carboxyl groups.

Racemic 4-(4-tert-butylphenyl)-2,6-dimethylcyclohex-3-enecarboxylic acid