Electronically excited carbon dioxide (CO 2 *) is known for its broadband emission, and its detection can lead to valuable information; however, owing to its broadband characteristics, CO 2 * is difficult to isolate experimentally, and its chemical kinetics are not well known. Although numerous works have monitored CO 2 * chemiluminescence, a full kinetic scheme for the excited species has yet to be developed. To this end, a series of shock-tube experiments was performed in H 2 -N 2 O-CO mixtures highly diluted in argon at conditions where emission from CO 2 * could be isolated and monitored. These results were used to evaluate the kinetics of CO 2 *, in particular the main CO 2 * formation reaction CO + O + M CO 2 * + M (R1). Based on collision theory, the quenching chemistry of CO 2 * was estimated for 11 collision partners. The final mechanism developed for CO 2 * consists of 14 reactions and 13 species. The rate for (R1) was determined to within about ±60% using low-pressure experiments performed in five different (H 2 -)N 2 O-CO-Ar mixtures, as follows:where R is the universal gas constant in cal/mol-K and T is the temperature in K. Final mechanism predictions were compared with experiments at low and high pressures, with good agreement at both conditions for the temperature dependence of the peak CO 2 * and the CO 2 * species time histories. Comparisons were also made with previous experiments in methane-oxygen mixtures, where there was slight overprediction of CO 2 * experimental trends, but with the results otherwise showing a dramatic improvement over an earlier mechanism. Experimental results and model predictions were also compared with past literature rates for CO 2 *, with good agreement for peak CO 2 * trends and slight discrepancies in CO 2 * species time histories. Overall, the ability of the CO 2 * mechanism developed in this work to reproduce a range of experimental trends represents an important improvement over the existing knowledge base on chemiluminescence chemistry. C