In this study, the interaction of two ionic liquids with hydrocarbons has been investigated. With this aim, (solid + liquid) equilibria (SLE) and (liquid + liquid) equilibria (LLE) for binary systems of {1-methyl-1-propyl-pyrrolidinium triflate [PMPyr][CF3SO3] + heptane, or benzene, or thiophene, or benzothiophene} and {N-butyl-4-cyanopyridinium tricyanomethanide [(BCNPy)-Py-4][TCM] + heptane, or toluene, or 2-methylthiophene, or benzothiophene} were measured at ambient pressure. A dynamic method was used over a broad range of mole fractions and temperatures from (T = 270 to 370) K. An upper critical solution temperature (UCST) was detected for all mutually immiscible systems. The immiscibility gap for [(BCNPy)-Py-4][TCM] in benzene and thiophene is larger than those for [PMPyr][CF3SO3]. Conversely, in heptane it is slightly larger for [PMPyr][CF3SO3]. The basic thermal properties of the pure ILs, i.e. melting and glass-transition temperatures as well as the enthalpy of fusion have been measured using a differential scanning microcalorimetry technique (DSC). The well-known NRTL model has been used to correlate the experimental SLE data points. (C) 2014 Elsevier Ltd. All rights reserved.