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Self-diffraction is a four-wave mixing process proportional to the square modulus of third-order nonlinearity susceptibility χ (3) , which is related to the material’s electronic and thermal properties. In this study, we investigate the wavelength dependence of the self-diffracted signal generated by a femtosecond pulsed laser in a dye solution to directly evaluate the electronic third-order nonlinear susceptibility spectrum. By accounting for absorption effects and phase matching conditions, we determine the | χ (3) | for different concentrations. Experimental results complemented with theoretical predictions show that, in the low absorption and thin sample limits, the signal reproduces the | χ (3) | spectral profile. These findings demonstrate the feasibility of measuring nonlinear susceptibility spectra arising solely from the bound-electronic response across a wide spectral range and for various compounds.