Terpene compounds include a wide variety of molecules with very different structures and physico-chemical properties. Monoterpenes are of interest because of their volatility and aromatic properties. Inclusion complexation of these molecules with cyclodextrins will lead to chemical and volatility protection and to a possible controlled release. In this study, reversed phase liquid chromatography was used to demonstrate that some terpenes can form inclusion complexes with β-cyclodextrin. The stability of these complexes was studied for aromatic, aliphatic, or acyclic terpenes with various mobile phases.