A commercial differential scanning calorimeter (DSC) was adapted to allow accurate isobaric heat capacity, c(p), measurements of cryogenic, high-pressure liquids. At (subcritical) temperatures between (108.15 and 258.15) K and pressures between (1.1 and 6.35) MPa, the standard deviation in the measured c(p) values was 0.005.c(p) for methane, 0.01.c(p) for ethane, and 0.015.c(p) for propane, which is comparable to both the scatter of c(p) data for these liquids measured using other techniques and with the scatter of those data sets about the reference equation of state (EOS) values. Three key modifications to the commercial DSC were required to enable these accurate cryogenic, high-pressure liquid c(p) measurements. First, methods of loading and removing the liquid from the calorimeter without moving the sample cell were developed and tested with high boiling temperature liquids; this modification improved the measurement repeatability. Second, a ballast volume containing a high-pressure vapor phase at constant temperature was connected to the DSC cell so that the liquid sample's thermal expansion did not cause significant changes in pressure. A third modification was required because the boil-off vapor from the liquid nitrogen used to cool the calorimeter resulted in a temperature inversion, and hence convection, along the tubing connecting the DSC's sample cell to the ballast volume, that lead to an unstable calorimetric signal at T > 130 K. The modifications to the specialized DSC were tested by measuring c(p) values for heptane, methylbenzene, and a heptane (1) + methylbenzene (2) mixture with x(1) = 0.38 at atmospheric pressure and temperatures of (228.15, 238.15, 303.15, and 313.15) K. The measured values had relative deviations from those measured adiabatically by Holzhauer and Ziegler (J. Phys. Chem. 1975, 79, 590-604) of less than 0.006.c(p), indicating that the specialized DSC could be used for liquids and liquid mixtures at conditions relevant to liquefied natural gas production.