Calorimetric, dielectric, and electrocaloric measurements have been performed on single-crystal samples of KH2PO4 in the neighborhood of the ferroelectric phase transition, and show that the transition is of first order, with a discontinuous entropy change of (0.0456-0.0059+0.0045)R and a change in the dielectric constant by a factor of 2. Calorimetric measurements in applied electric fields were also carried out, and show that the effect of an applied field is to shift the transition to higher temperatures and to broaden it. Calorimetric measurements on KD2PO4 are reported which can be combined with previously reported results to give the heat capacity for this material in the range 80-280°K. Comparison of the heat capacity of KH2PO4 and its deuterated isomorph allows estimates of the lattice heat capacity to be made. From this estimate, the entropy change associated with the ferroelectric transition is found to be (0.4000.036)R for KH2PO4 and (0.4570.034)R for KD2PO4. A significant feature of the comparison is the lack of evidence for the heat-capacity contribution above the transition predicted by theories of the Slater type. Comparison of the calorimetric data with the modified Slater theory due to Silsbee, Uehling, and Schmidt shows that this theory describes KD2PO4 better than it does KH2PO4. The differences between the theory and experiment are of the type predicted by the modifications of the theory which include tunneling motion of the protons. © 1969 The American Physical Society.