The present work takes advantage of the self-assembly process occuring along organogelation, to organize Second Harmonic Generation (SHG) active chromophores. To do so, three push-pull chromophores endowed with a dodecyl urea chain were synthesized and characterized. Their organogelating properties were studied in a wide range of solvents. Despite similar architectures, these derivatives exhibit very different gelling properties, from supergelation to absence of gelling ability. The utilization of the Hansen solubility parameters allows for observing clear relationships between the gelled solvents and critical gelation concentrations. By evaporating the solvents from the organogels, xerogel materials were prepared and systematically studied by means of optical and electron microscopies as well as SHG microscopy. These studies demonstrate the critical role of the solvent over materials structuring and allow generalizing the approach exploiting organogelation as a structuring tool to spontaneously organize push-pull chromophores into SHG-active materials.