The equation of state of the poly(propylene glycol) (PPG) ] water system has been measured using a vibrating tube densimeter in the intervals 0.1 O P/MPa O 40.0 and 298.15 O T /K O 328.15, and over the whole composition range. The PÈoÈT data can be well described by a generalized Tait equation. The results show that the e †ect of pressure on the relative molar volume is smaller than for both the PPG ] ethanol and PPG ] n-hexane systems. The excess volume is highly negative, and similar to that previously reported for poly(ethylene glycol) ] water. Increasing the pressure decreases both *GE and *HE. The corresponding states equation proposed by Huang and OÏConnell (Fluid Phase Equilibr., 1987, 37, 75) fails when applied to the present systems. Although the master curve proposed by Sanchez et al. (Macromolecules, 1993, 26, 4234) does not describe the PÈoÈT surface of PPG ] water with the same degree of precision as that for the PPG ] n-hexane or of PPG ] ethanol, it still can be useful for estimating high-pressure data from low-pressure isothermal compressibility data.