posted on 2020-01-21, 21:12authored byMarwah Aljohani, Patrick McArdle, Andrea Erxleben
Vanillin
and vanillate esters are widely used as flavorings in
the food industry, and the vanillin derivative zingerone is one of
the compounds found in the spice ginger. Neither the growth of single
crystals of zingerone or methyl or ethyl vanillate nor their crystal
structures or the crystal structures of their hydrates have been reported.
In this paper a detailed study of the crystallization of methyl vanillate,
ethyl vanillate, and zingerone is described and the relationship among
crystal growth, habit, and intermolecular interactions in the crystal
lattice is discussed. Adventitious or deliberately added water suppressed
the crystal nucleation and growth of zingerone from cyclohexane solution.
Good-quality single crystals of zingerone can be grown from a cyclohexane
solution in closed vials if water is excluded. It was not possible
to isolate a hydrate of zingerone. In contrast, the crystallization
of methyl and ethyl vanillates from cyclohexane is not affected by
adventitious water from the air and monohydrates are easily isolated.
The crystal structures of zingerone, methyl and ethyl vanillates,
and the monohydrates of the vanillates have been determined and analyzed
using the PIXEL program. Observed crystal morphologies have been rationalized
using intermolecular interaction energies and slice attachment energy
calculations.