Variations in the molar retention volume of organic solutes on thirteen tetra-n-butylammonium salts with a common liquid temperature range are correlated with the properties of the anion. The anions studied include the chloride, bromide, nitrate, nitrite, methanesulfonate, trifluoromethanesulfonate, ethanesulfonate, 4-toluenesulfonate, sulfamate, thiocyanate, picrate, pentacyanopropenide, and tetra-n-butylborate. The high melting points and poor thermal stabilities of camphorsulfonate, dihydrogenphosphate, hydrogensulfate,
and perrhenate precluded their use. The properties of the anions have only small influences on the magnitudes of dispersive, orientative, and proton-donor interactions with the test solutes. Orientative interactions are strong for polar solutes but vary little with anion structure. There was no correlation between the dipole moment of the tetra-n-butylammonium salts and the retention of polar solutes. The structures of the anion do, however, have large influences on the retention of proton-donor solutes. For these solutes, a good correlation was found between molar retention volume and the basicity of the anions, represented by their pKa values in aqueous solution.