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Investigation of the solid-state polymorphic transformations of piracetam

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posted on 2023-01-04, 11:46 authored by Anthony Maher, Colin C. Seaton, Sarah HudsonSarah Hudson, Denise M. Croker, Åke C. Rasmuson, Benjamin K. Hodnett
The solid-state polymorphic transformations of 2-oxo-1-pyrrolidine acetamide (Piracetam) were investigated using a combination of off-line and on-line techniques; Differential Scanning Calorimetry (DSC), High Temperature X-ray Diffraction (HT-XRD), thermal analysis and Hot Stage Optical Microscopy. Form II and Form III were each observed to transform directly to Form I upon heating, with Form II transforming at a slightly lower temperature. The transformation of both polymorphs to Form I was observed to cause physical cracking of the crystals as well as changing the optical properties. Form I consistently transformed to Form II when cooled. The molecular rearrangements required for the transformation from Form I to Form II were found to be more energetically favourable than those required for the transformation to Form III. The transformation from the metastable Form II to the stable Form III was not observed in the solid state, while the Form II – Form III transition temperature was found to be higher than the transition temperature of both polymorphs to Form I.

History

Publication

Crystal Growth & Design;12(12), pp 6223-6233

Publisher

American Chemical Society

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peer-reviewed

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SFI

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This is the author’s version of a work that was accepted for publication in Crystal Growth & Design. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Cryst. Growth Des, 12(12), pp. 6223-6233, http://dx.doi.org/10.1021/cg301418c. Reprinted with permission from American Chemical Society ©2012 ACS

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English

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