The solubilities of aminocaproic
acid in four monosolvents (isopropanol,
methyl acetate, ethyl acetate, and water) and three binary solvents
(methanol–water, ethanol–water, and dimethylformamide–water)
were measured by the static analytical method from 283.15 to 323.15
K at atmospheric pressure. In monosolvents, the solubility increases
with the increase of temperature. Also, the solubility of aminocaproic
acid in water is much higher than that in other organic solvents.
In binary solvents, the solubility increases with the increase of
the temperature and the mole fraction of water. The solubility data
was well correlated by the Apelblat equation, λh equation, and NRTL equation, and the mixing properties of enthalpy,
Gibbs energy, and entropy have also been discussed.