Abstract:In the present study, we have described the synthesis and characterisation of the theophylline hydrate (Theo hydrate), cocrystal (Theo–Phen·2H2O) and hydrated sodium co-crystal of theophylline (Na–(Theo)2ClO·2H2O), where Theo = theophylline and Phen = 1,10-phenathroline.
“…2c) that contribute to a significant stabilization of this hydrated sodium cocrystal (Na–(Theo) 2 –ClO·2H 2 O), compared with the traditional hydrated cocrystal without the participation of sodium (Theo–Phen·2H 2 O). 86 Furthermore, the employment of halogen-bond synthons in cocrystal design (Fig. 2d) also successfully transformed the highly volatile liquid iodoperfluoroalkanes into crystalline materials with long-term stability.…”
Section: Cocrystal Strategy To Different Environmental Stressmentioning
Cocrystallization has been recognized as one of the most successful approaches to address stability problems of active pharmaceutical ingredients (APIs) in the past few decades. However, scant attention has been...
“…[24][25][26] Its modulation has enabled the enhancement of the thermal stability and processability of the determined molecules through the formation of cocrystals. [27][28][29] Indeed, our group has previously studied the formation of cocrystals based on the acid⋯amide 30 and acid⋯pyridine heterosynthons 31 and the correlation of the crystal packing with their melting point values. 31 Therefore, aiming to extend our knowledge on the structure-property relationship of cocrystals focusing on the melting point, we have selected a liquid and a solid pyridine derivative (dPy), namely 4-acetylpyridine (4-Acpy) and 2-hydroxypyridine (2-OHpy), respectively.…”
The melting point of a liquid and a solid pyridine derivative has been modified using the cocrystal formation approach by combination with two carboxylic acids. Their crystal packings have been analyzed and correlated with their thermal stability.
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