Raman spectroscopy of dispersed vitrinites needs polished surfaces to safely identify organic particles in whole rock samples. Carbonaceous matter (CM) is very sensitive to the polishing process which leads to erroneous Raman spectra of these materials. It is unknown to which extent Raman spectra of low ordered CM are influenced by the polishing process. Therefore, vitrinites of high volatile bituminous coal, through anthracite to semi graphite rank to graphitic CM were analyzed by multi-wavelength Raman spectroscopy and measured for minimum and maximum reflectance. A step-wise preparation and measuring protocol allows us to access at which point the Raman spectra are altered by sample preparation. The effect of polishing on the Raman spectra of vitrinites is not significant up to maximum reflectance values of similar to 7%. The multi-wavelength approach shows that short-wavelength lasers (488 nm and less) invoke far less fluorescence background than long-wavelength lasers, which permits us to measure very low mature vitrinites. Wavelength-dependent frequency shifts in the vitrinite Raman spectra reconstruct a two stage evolution of aromatic compounds during organic metamorphism. The first stage shows a wavelength independent downshift of the defect-band (D -band) from similar to 1370 to 1330 cm(-1), which is assumed to be related to the progressive growth of linear aromatic structures. The second stage is characterized by diverging D -band positions, which is caused by the growth of compact polycyclic aromatic hydrocarbons. Consequently, a strong linear correlation between the reflectance values and the derived Raman spectroscopic parameters was found. Because the comparison was conducted on the single grain level, it is shown that the scaled total area (STA) Raman parameter relates to the true maximum vitrinite reflectance. Thus, a linear and robust maturity index, which covers a maximum vitrinite reflectance range of ca. 1 to 7%, is established. (C) 2015 Elsevier B.V. All rights reserved.