Supported chromium catalysts with different support composition are studied by electron spin resonance spectroscopy (ESR), thermogravimetrical analysis (TGA), and Al-27 magic angle spinning nuclear magnetic resonance (MAS-NMR). With ESR, the presence of Cr5+ (gamma-signal) and two types of Cr3+ (delta- and beta-signals) are observed; however, their concentrations are support-, loading-, and pretreatment-dependent. The Cr5+ loading increases with the alumina content of the support and can be maximized after moderate reduction temperatures and by using relatively low Cr loadings. Dispersed Cr3+ (delta-signal) is formed by reduction, and its amount increases with Al content of the support, Cr loading, and reduction temperature. On silica-alumina and alumina it is stable against recalcination. Cr2O3-like clusters (beta-signal) are observed only on Cr/alumina after reduction and recalcination. TGA analysis indicates an increasing interaction strength between Cr and the support from silica over silica-alumina to alumina. The quenching of the Al-27 lines by paramagnetic Cr3+ was observed by Al-27 MAS-NMR measurements on the recalcined samples. This quenching effect was stronger on the Cr/alumina sample than on the Cr/silica-alumina samples, indicating Cr3+ substitution in octahedral Al sites. The observed differences in redox behavior and dispersion of Cr between the catalysts are discussed in terms of the support properties and in relation with previous results obtained by diffuse reflectance spectroscopy (DRS).