In this contribution,
the 5,7-dibromo-8-hydroxyquinoline
solubility in neat N,N-dimethylaniline
(DMA), n-butanol, methanol, N,N-dimethylformamide (DMF), ethanol, 2-butanone, n-propanol, ethyl acetate, isopropanol, acetone, 1-methyl-2-pyrrolidinone
(NMP), toluene, and 1,4-dioxolane was experimentally obtained using
the shake-flask method covering a temperature range from 288.15 to
328.15 (333.15) K under ambient pressure of p = 101.2
kPa. The solubility values in the mole fraction scale of 5,7-dibromo-8-hydroxyquinoline
in the studied thirteen solvents increased as the experimental temperature
increased and ranked as NMP > DMA > DMF > 1,4-dioxane >
ethyl acetate > toluene > acetone > 2-butanone > n-butanol > n-propanol > ethanol
> isopropanol > methanol. The influence of interactions of solvent–solvent
molecules and solvent–solute molecules on the 5,7-dibromo-8-hydroxyquinoline
solubility was examined by the use of the linear solvation energy
relationship according to the solvent descriptors. The obtained solubility
data was correlated mathematically through the NRTL model, λh equation, Apelblat equation, and Wilson model. The acquired
values of root-mean-square deviation and relative average deviation
were no more than 23.53 × 10–4 and 5.18 ×
10–2, respectively. In general, the values of relative
average deviation attained through the Apelblat equation were smaller
than that attained through the other models/equations for a certain
neat solvent. The mixing property, infinitesimal concentration activity
coefficient, and reduced excess enthalpy were resulted as well.