The recent discovery of organic matter exposed in patches on the surface of the asteroid Ceres has sparked considerable interest in its prospect as an emerging astrobiological target. The dwarf planet's surface is also characterized by a pervasive display of salt minerals, which are suggestive of briny fluids at depth and ongoing geological activity that resulted in their emplacement. While these salt-rich subsurface liquid reservoirs can present enticing conditions for prebiotic chemistry to emerge, the connection between dissolved organic materials and the associated salt minerals upon exposure to Ceres' surface environment has not yet been established. Here, we explore this fundamental relationship by investigating the chemistry of putative organicbearing brines relevant to Ceres (composed of sodium, ammonium, carbonate, and chloride ions) upon freezing using infrared (IR) reflectance and Raman spectroscopies, specifically focusing on two representative amino acids (glycine and aspartic acid) and an N-containing aliphatic compound (hexylamine). The results indicate that the presence of these organic species in the brines leads to the formation of CO 2 (isolated in the water ice matrix) when flash-freezing to liquid nitrogen temperatures. In particular, the two amino acids produce significantly more CO 2 compared to the hexylamine-brine mixture. Slow-freezing conditions, on the other hand, do not exhibit such a behavior. The bicarbonate anions in solution (rather than the amino acids themselves) are confirmed to be the source of CO 2 by isotopic substitution experiments. Raman measurements subsequently hint at a possible reaction pathway involving the formation of a carbamate intermediate. These results not only exemplify the potentially important role of organic-salt interactions in Ceres' evolution, but also provide insights into the fate of organics and future detection strategies of organic deposits on ocean worlds.