The rotational dynamics of nile red has been studied in polar protic, polar aprotic and non-polar solvents. In the non-polar and the aprotic solvents, with the exception of long alkanenitriles, the rotation dynamics is consistent with the prediction of the Stokes-Einstein-Debye hydrodynamics theory for slip and close to the stick boundary condition, respectively. However in protic solvents, the rotation dynamics can be explained in terms of the Stokes-Einstein-Debye hydrodynamics theory under stick boundary condition only if solvent attachment via hydrogen bonding is assumed. The anomalous behaviour observed in longer alkanenitriles has been assigned to the formation of a reverse micelle-like solvation layer around nile red.