Single phase mixed zirconium phosphate phenylphosphonates, ZrP(PP)(x), were prepared by two different synthetic approaches: reaction of gels of nanosized alpha-zirconium phosphate in propanol with solutions of phenylphosphonic acid (H2PP), leading to the topotactic exchange of monohydrogen phosphate groups with phenylphosphonate groups, and precipitation from propanol solutions of H2PP, phosphoric acid, and zirconyl propionate. In both cases, propanol intercalated compounds were obtained. The x values of the ZrP(PP)(x) materials prepared by topotactic anion exchange ranged from 0.37 to 0.56 for (H2PP/Zr) molar ratios in the range 0.52-4.16 and [H2PP] = 0.1 M, while a maximum x value of 0.73 was only reached at 60 degrees C, with (H2PP/Zr) = 4.16 and [H2PP] = 0.31 M. Direct precipitation of ZrP(PP)(x) provided samples with 0.13 <= x <= 1.54, for H2PP molar fractions in the range 0.05-0.5 and (P/Zr) molar ratio = 6. At 90% relative humidity, the (H2O/Zr) molar ratio for the precipitated ZrP(PP)(x) powder samples increased in the range 1.3-3.0 with increasing x and resulted in being higher than that of nanosized ZrP (0.8). The analysis of the X-ray diffraction patterns of the gel and powder samples, together with the hydration data of the powder samples, suggested a structural model in which the random distribution of the phosphate and phenylphosphonate groups creates cavities which can accommodate propanol molecules in the gel samples and water molecules in the hydrated powder samples.