The pressure induced reactivity of carbon monoxide was investigated in a wide temperature range (100-400 K) completely avoiding any irradiation of the sample with visible or higher frequency light. FTIR spectroscopy was employed to monitor the reaction and infrared sensors for measuring the pressure. With this approach we have been able to separate the effects of the three variables (P, T and hnu) that establish the conditions for the occurrence of the chemical reaction. A new instability boundary, not affected by the photoactivation of the reaction, is provided. The reaction has been studied in three different crystal phases (epsilon, delta, and beta), but the small differences in the reaction products are ascribable to the temperature changes rather than to the crystalline arrangement. For T<300 K the analysis of the IR spectra reveals the formation of an extended amorphous material formed, according to the vibrational assignment and to the kinetic data, by polycarbonyl linear chains containing a large amount of anhydride groups. For T>or=300 K the formation of carbon dioxide and epoxy rings, and the simultaneous decrease of carbonyl species, let suppose a decarboxylation of the extended solid product. Once exposed to the atmosphere, the reaction product readily and irreversibly reacts with water giving rise to carboxylic groups.