The
solubility of pharmaceutical compounds in solvents and their
mixtures determines their separation and purification in the chemical
industries. In this work, the solid–liquid equilibria measurements
for solubility of cetirizine hydrochloride and deferiprone in five
single pure solvents as acetonitrile, ethanol, acetic acid, sulfolane,
and ethyl acetate, and their binary mixtures, including ethanol +
ethyl acetate, acetonitrile + ethanol, acetonitrile + acetic acid,
and acetonitrile + sulfolane, were made at temperatures of 283.15–323.15
K and atmospheric pressure. The mole fraction solubility of both pharmaceuticals
in all monosolvents is enhanced by an increase in temperature. In
addition, two empirical equations of modified Apelblat and λh, and three local composition models of Wilson, nonrandom
two-liquid (NRTL), and universal quasi-chemical (UNIQUAC) were employed
to correlate the measured solubility data. The UNIQUAC model and the
modified Apelblat equation showed the most proper functions that could
be used to correlate the solubility data for the present pure and
mixed-solvent systems, respectively.