Supercritical carbon dioxide (CO2) is often used as a process fluid for enhanced oil recovery. The storage of carbon dioxide in underground formations is a potential way of mitigating climate change during a transition period to more sustainable energy sources. Combining injection with subsequent trapping of the non-wetting supercritical carbon dioxide phase in the pores of a depleted reservoir is a promising scheme for allowing the continued use of fossil fuels with minimal environmental consequences. The design of such processes is ultimately linked to the confined behaviour of the fluids in question at reservoir conditions, which is largely controlled by interfacial forces. Measurements of the relevant interfacial tensions for systems containing alkanes, carbon dioxide and water are currently limited and inconsistent while models usually fail to capture the pressure dependence of the interfacial tension. In this work, a density functional theory based on the SAFT-VR equation of state was used to predict the interfacial tension of (H2O+CO2+n-alkane) binary systems over wide ranges of temperature and pressure. The comparison with a new set of reported experimental data of three (n-alkane+CO2) systems at pressures up to the critical points, as well as with the (H2O+CO2) system at pressures up to 60MPa, for a temperature range of (298–443)K, is discussed.