Magnesium potassium phosphate cements (MKPCs) are prepared by the acid-base reaction of dead burned magnesia (MgO) and monopotassium phosphate (KH2PO4). Low-pH cementitious materials such as MKPCs are currently of interest for the geological disposal of nuclear waste. MKPCs have advantages such as high early strength, high bonding strength, small drying shrinkage, low permeability, and high sulfate resistance. According to the results of previous studies, it is known that cesium, strontium, and cobalt are immobilized in the form of MgCsxK1−xPO4·6H2O, MgxSr1−xKPO4·6H2O, and Co3(PO4)2, respectively, in MKPCs. However, these results were predicted based on thermodynamic data, not directly observed precipitates to clearly show the evidence. Therefore, in this study, we directly analyzed the immobilized forms of Cs, Sr, and Co, respectively. CsNO3, Sr(NO3)2, and Co(NO3)2·6H2O powders (0.3 mol each) were mixed individually in each of the MKPC suspensions. The suspensions in which KH2PO4 was dissolved were pH 4.3 and the dissolution of MgO decreased the H+ concentration, raising the pH close to 11. The hydration products according to pH evolution in the MKPC suspensions were analyzed, and the change in the concentration of ions in the aqueous solution was also measured. An aqueous solution was obtained using a syringe filter (0.45 μm) to analyze the ion concentrations in the solution of the suspension. The collected solutions were diluted with nitric acid and analyzed using inductively coupled plasma mass spectrometry. To characterize the solid phases, the suspensions were obtained with a pipette at specific times and filtered under a vacuum in a Buchner funnel. Because the amounts of hydration products including Cs, Sr, and Co were small, it was not observed by XRD and TGA analysis, but their components could be analyzed by SEM-EDS. The final precipitate forms of Cs, Sr, and Co in the MKPC matrix are MgCsPO4·6H2O, SrHPO4, and Co3(PO4)2·8H2O, respectively.