Hydrated Mg-carbonate minerals form during the weathering of ultramafic rocks, and 2 can be used to sequester atmospheric CO 2 to help combat greenhouse gas-fueled climate change. Optimization of engineered CO 2 sequestration and prediction of the composition and stability of Mg-carbonate phase assemblages in natural and engineered ultramafic environments requires knowledge of the solubility of hydrated Mg-carbonate phases, and the transformation pathways between these metastable phases. In this study, we evaluate the solubility of nesquehonite [MgCO 3 •3H 2 O] and dypingite [Mg 5 (CO 3) 4 (OH) 2 •(5 or 8)H 2 O] and the transformation from nesquehonite to dypingite between 5°C and 35°C, using constanttemperature, batch-reactor experimentals.. The logarithm of the solubility product of nesquehonite was determined to be:-5.03±0.13,-5.27±0.15, and-5.34±0.04 at 5°C, 25°C, and 35°C, respectively. The logarithm of the solubility product of dypingite, never reported before, was determined to be:-34.95±0.58 and-36.04±0.31 at 25°C and 35°C, respectively, with eight waters of hydration. The transformation from nesquehonite to dypingite was temperature-dependent, and was complete within 57 days at 25°C, and 20 days at 35°C, but did not occur during experiments of 59 days at 5°C. This phase transformation appeared to occur via a dissolution-reprecipitation mechanism; external nesquehonite crystal morphology was partially maintained during the phase transformation at 25°C, but was eradicated at 35°C. Together, our results facilitate the improved evaluation of Mg-carbonate mineral precipitation during natural and engineered ultramafic mineral weathering systems that sequester CO , and 20 for the first time allow assessment of the saturation state of dypingite in aqueous solutions. 21