Rotational and vibrational spontaneous Raman scattering (SRS) spectra of H 2 , N 2 and H 2 O have been measured in H 2 -air flames at pressures up to 30.4 bar as a first step towards establishing a comprehensive Raman spectral database for temperatures and species in high-pressure combustion. We have obtained an initial set of measurements that indicate the spectra are of sufficient quality in terms of spectral resolution, wavelength coverage and signal-to-noise ratio for use in the development of transferable standards for the cross-talk calibration matrix. The fully resolved Stokes and anti-Stokes shifted spectra were collected in the visible wavelength range (400-700 nm) using pulse-stretched 532 nm excitation and a spectrograph fitted with a non-intensified CCD detector and a high-speed shutter. Temperatures were determined via the intensity distribution of rotational H 2 lines at stoichiometric and fuel-rich conditions. A discussion of the temperature measurement accuracy in terms of the number of laser shots, including a single-shot measurement, is presented. Theoretical Raman spectra of hydrogen were calculated using a semi-classical anharmonic-oscillator model with recent pressure broadening data and were compared with experimental data. The data and simulation showed good agreement at different equivalence ratios and pressures and indicate that high-J rotational lines of H 2 may interfere with the N 2 vibrational Q-branch lines, which could lead to errors in N 2 -Raman thermometry based on the line-fitting method. In addition, the relative intensities of the O-and S-branches to the Q-branch were determined theoretically and the result indicates that further studies of spectral interferences including contributions from O-and S-branches should be pursued. Finally, from a comparison of N 2 Q-branch spectra in lean H 2 -air flames at nearly atmospheric (1.2 bar) and high pressure (30.4 bar), we found no significant line-narrowing or -broadening effects at a spectral resolution of 0.04 nm.