A detailed analysis is reported of high resolution I.R. spectra of CF3C1 (Freon 13, chlorotrifluoromethane) in the 750-800cm -1 range obtained by Fourier transform and diode laser spectroscopy. A comparison is made between hot-band transitions starting from a non-degenerate vibrational level (V 2 "~ ' i~ 3 --lP3) and those from two-fold degenerate levels (v 2 + v 5 -v 5 and v2 + v6 -v6). For the latter the effect of vibrational excitation on the Coriolis constant A( has been observed. The rotational analysis of the v2 + v6 -v6 band of CF33SC1 has been performed in the P-and R-branches up to J = 32 and 34 respectively. Rotational/-doubling in both v 6 and v 2 + v 6 state causes a splitting of the kl = 1 transitions and observable shifts in transitions with other (low) kl. A least-squares fit of more than 500 lines yielded molecular constants for the v 2 + v 6 state.