In this paper, the formation of colloidal species of fullerene C 70 in organic solvents was studied. The examining of the UV-visible spectra was accompanied by particle size analysis using dynamic light scattering, DLS. Stock solutions of C 70 in non-polar toluene and n-hexane were diluted with polar solvents acetonitrile and methanol. The appearance of colloidal species with a size within the range of ≈ 50-500 nm is accompanied by alterations of the absorption spectra. In the toluene-acetonitrile and toluene-methanol binary mixed solvents at 25 o C, the absorption spectra of C 70 (5×10-6 M) tend to retain the features of the spectrum in neat aromatic solvent even if the C 70 molecules are gathered into colloidal aggregates. Earlier such phenomenon was observed for C 60 in benzeneacetonitrile and toluene-methanol solvent systems. This gives support to the idea of rather stable primary solvate shells formed by aromatic molecules around the fullerene molecules. The behavior of C 70 in toluene mixtures with methanol was compared with the earlier reported results from this laboratory for the C 60 fullerene in the same solvent system. The study of n-hexane-methanol mixtures was performed at elevated temperature because of limited miscibility of these solvents at 25 o C. Accordingly, the C 70-toluene-methanol system was also examined at 40 o C. A small but distinctly noticeable difference was revealed. Whereas in the case of the last-named system, the absorption spectrum typical for molecular form of C 70 is still observable when colloidal species are already present in the solution, the turning-point between molecules and colloids as determined by both UVvisible spectra and DLS coincides for the n-hexane-methanol binary mixed solvent. Hence, the solvation shells formed by the aliphatic solvent around C 70 are less stable as compared with those formed by toluene. Finally, the absorption spectra of C 70 in the mixed solvents toluene-n-hexane were analyzed. These data give some support to the assumption of preferable solvation of the C 70 molecules by the aromatic co-solvent.