The structural dynamics of poly͑propylene-glycol͒ of molecular weight M W ϭ4000 have been investigated over a large temperature range 10-375 K and in a wide dynamical window, corresponding to 10 Ϫ3 -10 14 Hz, using various light-scattering techniques. The slow dynamics were investigated using a wide time-range photon-correlation spectroscopy; for the faster dynamics a combination of interferometric and grating spectrometer techniques were used. We observe four distinguishable kinds of dynamics; ͑i͒ slow normal-mode dynamics, ͑ii͒ the main (␣) relaxation which is related to the viscosity, ͑iii͒ a faster ͑͒ relaxation, and ͑iv͒ a low-frequency vibrational peak. The data are discussed in relation to the mode-coupling theory ͑MCT͒ for the liquid-glass transition. Surprisingly, the slow dynamics observed using the PCS technique close to the glass transition temperature T g are found to be in good agreement with predictions of MCT and a T c ϭ236 K can be extracted. In contrast, the high-frequency data taken above T c are not consistent with MCT. In this range a strong vibrational peak, the so-called boson peak, seriously affects the relaxational spectrum and simple MCT analysis cannot be applied. This finding is in agreement with recent light-and neutron-scattering investigations of other hydrogen-bonded intermediate glass formers and also strong covalently bonded systems.