4.7 Article

New Saccharin Salt of Chlordiazepoxide: Structural and Physicochemical Examination

Journal

Publisher

MDPI
DOI: 10.3390/ijms231912050

Keywords

chlordiazepoxide; saccharin; organic salt; Powder X-ray Diffraction (PXRD); Single Crystal X-ray Diffraction (SCXRD); Differential Scanning Calorimetry (DSC); Thermogravimetric Analysis (TGA); Fourier Transform Infrared (FT-IR); Raman spectroscopy

Funding

  1. Ministry of Science and Higher Education, Poland [02-0015/07/505]

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The research aimed to prepare an organic salt of chlordiazepoxide with saccharin by obtaining a crystalline salt through grinding and crystallization methods. Various analytical techniques confirmed the structure and properties of the salt formed between chlordiazepoxide and saccharin.
Since the formation of organic salts can improve the solubility, bioavailability, and stability of active pharmaceutical ingredients, the aim of this work was to prepare an organic salt of chlordiazepoxide with saccharin. To achieve this goal, the saccharin salt of chlordiazepoxide was obtained from a physical mixture of both components by grinding them with a small volume of solvent and by crystallizing them with complete evaporation of the solvent. The resulting salt was examined by methods such as Powder X-ray Diffraction (PXRD), Single Crystal X-ray Diffraction (SCXRD), Differential Scanning Calorimetry (DSC), Thermogravimetric Analysis (TGA), Fourier Transform Infrared (FT-IR), and Raman spectroscopy. The results of the studies proved that saccharin salt of chlordiazepoxide crystallizes in the orthorhombic Pbca space group with one chlordiazepoxide cation and one saccharin anion in the asymmetric unit. In the crystal of the title compound, the chlordiazepoxide cation and the saccharin anion interact through strong N-H center dot center dot center dot O hydrogen bonds and weak C-H center dot center dot center dot O hydrogen bonds. The disappearance of the N-H band in the FT-IR spectrum of saccharin may indicate a shift of this proton towards chlordiazepoxide, while the disappearance of the aromatic bond band in the chlordiazepoxide ring in the Raman spectrum may suggest the formation of intermolecular hydrogen bonds between chlordiazepoxide molecules. The melting point of the salts differs from that of the starting compounds. Thermal decomposition of the salt begins above 200 degrees C and shows at least two overlapping stages of mass loss. In summary, the results of the research showed that the crystalline salt of the saccharin and chlordiazepoxide can be obtained by various methods: grinding with the addition of acetonitrile and crystallization from acetonitrile or a mixture of methanol with methylene chloride.

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