We review in this work specific-heat experiments, that we have conducted on different hydrogen-bonded glasses during last years. Specifically, we have measured the lowtemperature specific heat C p for a set of glassy alcohols: normal and fully-deuterated ethanol, 1-and 2-propanol, and glycerol. Ethanol exhibits a very interesting polymorphism presenting three different solid phases at low temperature: a fully-ordered (monoclinic) crystal, an orientationally-disordered (cubic) crystal or 'orientational glass', and the ordinary structural glass. By measuring and comparing the low-temperature specific heat of the three phases, in the 'boson peak' range 2-10 K as well as in the tunneling-states range below 1K, we are able to provide a quantitative confirmation that "glassy behavior" is not an exclusive property of amorphous solids. On the other hand, propanol is the simplest monoalcohol with two different stereoisomers (1-and 2-propanol), what allows us to study directly the influence of the spatial rearrangement of atoms on the universal properties of glasses. We have measured the specific heat of both isomers, finding a noteworthy quantitative difference between them.Finally, low-temperature specific-heat data of glassy glycerol have also been obtained. Here we propose a simple method based upon the soft-potential model to analyze low-temperature specific-heat measurements, and we use this method for a quantitative comparison of all these data of glassy alcohols and as a stringent test of several universal correlations and scaling laws suggested in the literature. In particular, we find that the interstitialcy model for the boson peak [A. V. Granato, Phys. Rev. Lett. 68 (1992) 974] gives a very good account of the temperature T max at which the maximum in C p /T 3 occurs.