Primary or secondary cyclic amine + alkane mixtures have been investigated in the framework of the ERAS (Extended Real Associated Solution) model. The corresponding ERAS parameters are reported. All the amines considered have the same equilibrium constant (K-A = 0.75). Cyclopropylamine, cyclopentylamine, cyclohexylamine and pyrrolidine are characterized by the same enthalpy of self-association (Delta h(A)* = -15 kJ mol(-1)). Piperidine and hexamethyleneimine show a less negative Delta h(A)* value (-13 kJ mol(-1)). Experimental data on excess enthalpies, H-m(E), volumes, V-m(E), and isobaric heat capacities, C-pm(E), reveal the existence of physical interactions and structural effects in the studied solutions. The latter lead to values of self-association of pure amines, Delta v(A)*, which may depend on the solvent in systems with a given amine. Although the model overestimates the Delta h(A)* values, the relatively high values of the physical parameters X-AB remark the importance of physical interactions. ERAS describes correctly the excess functions H-m(E), V-m(E), C-pm(E) and G(m)(E) (molar Gibbs energy), and the enthalpy of vaporization of pure amines. Nevertheless, discrepancies with experimental data are found for the concentration dependence of V-m(E) and G(m)(E) of some mixtures including cyclic primary amines. (C) 2013 Elsevier B.V. All rights reserved.