This paper presents a comparison of the absolute infrared absorption intensities in the liquid and gas phases for the four infrared active fundamentals of benzene. In Herzberg’s notation these are nu(12) (similar to 3070 cm(-1)), nu(13) (similar to 1479 cm(-1)), nu(l4) (similar to 1036 cm(-1)), and nu(4) (similar to 675 cm(-1)). Published data are used, including the recently published spectra of liquid benzene that have been accepted by the International Union of Pure and Applied Chemistry as secondary intensity standards. The present results agree qualitatively with the conclusions drawn in 1970 that the intensity A(j) of nu(l2) is much smaller for the liquid than for the gas, and those of nu(13) nu(14), and nu(4) are all larger for the liquid. The inclusion of measurements made since 1970 should make the quantitative results reported here the most reliable. However, two quite different values have been reported in the 1980’s for the intensity of nu(14) in the gas phase, and both are considered. The comparison for nu(14) is also complicated by the existence of weak bands in the spectrum of the liquid that are not observed in that of the gas. It is noted in this work that the traditional comparison, of the areas under the molar absorption coefficient spectra, A(j), for the gas and liquid through the Polo-Wilson equation, has the drawback that the ratio expected if the dipole moment derivative is unchanged is different for each band as well as for each liquid. A much more convenient ratio, that equals unity for all bands of all liquids under the traditional assumptions, is proposed through the imaginary molar polarizability spectrum of the liquid. The magnitudes of the transition moments and the dipole moment derivatives with respect to the normal coordinates under the double harmonic approximation are calculated from the measured intensities for the gas and liquid phases. It is found that the dipole moment derivative of nu(12) is 24% smaller in the liquid than in the gas and that of nu(13) is 18% larger. The dipole moment derivative of nu(4) is unchanged by condensation. The change in the dipole moment derivative of nu(14) is not clear, because of the uncertainty in the gas phase intensity and because of the uncertain origin of the intensity of the additional bands in the liquid.