“…The penicillins can be considered as hydrotropes or hydrotropic agents if we considered that the term comprises hydrophilic and hydrophobic moieties, with the hydrophobic moiety being typically too small to induce micelle formation [33], and that the hydrotrope molecules are assumed to aggregate by a stacking mechanism of the planar aromatic ring present in their chemical structure, as is the case for the two penicillins [33]. The two penicillins differ in one extra chlorine atom in the meta position with respect to the first on the aromatic benzene ring of dicloxacillin if compared to cloxacillin, which has been key in providing different psychochemical properties for the two hydrotropes [34][35][36]. Previous studies have shown that these penicillins aggregate in aqueous solution by stacking with a low aggregation number that can be detected as a discontinuity of the concentration dependence of the physicochemical properties of the solution: conductivity, sound velocity, light scattering, etc.…”