posted on 2012-08-01, 00:00authored byRanjit Thakuria, Suryanarayan Cherukuvada, Ashwini Nangia
The solid-state structural landscape of bioactive compound
pyrogallol (1,2,3-benzenetriol) is studied. We report crystal structures
of pyrogallol, its 0.25 hydrate, and a few cocrystals with aromatic
N-heterocycles. The hydroxyl groups of pyrogallol can adopt different
conformations in the gas phase and in crystalline modifications, for
example, stable conformer “A” in pyrogallol and its
hydrate, whereas metastable conformer “C” in cocrystals
with isonicotinamide and nicotinamide. The occurrence of high Z′ (maximum of five quinoline and three pyrogallol
molecules in cocrystal 6a) and variable stoichiometry
of components in cocrystals (e.g., pyrogallol–isonicotinamide
1:2 and 2:1 in 4a and 4b, pyrogallol–quinoline
3:5 and 2:3 in 6a and 6b) is a unique and
novel observation in these structures. Grinding and slurry experiments
confirmed that the high Z′ cocrystal is quite
stable and it does not transform to a low Z′
higher symmetry structure. Given the biological and pharmacological
functions of pyrogallol, a naturally occurring ingredient of the Indian
gooseberry, solubility and dissolution rates of pyrogallol and its
cocrystals were compared in water.