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Febantel: looking for new polymorphs
- Source :
- Journal of Thermal Analysis and Calorimetry. 130:1605-1612
- Publication Year :
- 2017
- Publisher :
- Springer Science and Business Media LLC, 2017.
-
Abstract
- The aim of this work was to search for new polymorphic forms of febantel, an anthelminthic drug of great present interest for the veterinary industry. Solvent-based recrystallization, thermal and mechanical treatments and spray drying were chosen to discover new solid forms. The solids obtained were physicochemically characterized by thermal techniques (DSC and TG), FTIR spectroscopy, laboratory and synchrotron X-ray powder diffraction and scanning electron microscopy. Our work leads to obtain a new solid form never described in the literature. In particular, the new polymorph was obtained by the anti-solvent method and the crystallization from isopropanol. The experimental conditions of crystallization favorable to the formation of the highest amount of the new solid phase were selected. The new phase shows a thermal, spectroscopic and diffractometric behavior unique. Furthermore, the preliminary structure investigation suggests two possible crystal systems: an orthorhombic or a monoclinic one, with really comparable lattice parameters and cell volume. Measurements put into evidence that the new phase is a metastable polymorph that is in monotropic relationship with the stable and known form.
- Subjects :
- Materials science
Crystal system
Recrystallization (metallurgy)
02 engineering and technology
010402 general chemistry
021001 nanoscience & nanotechnology
Condensed Matter Physics
01 natural sciences
0104 chemical sciences
law.invention
Crystallography
law
Spray drying
Metastability
Orthorhombic crystal system
Physical and Theoretical Chemistry
Crystallization
0210 nano-technology
Powder diffraction
Monoclinic crystal system
Subjects
Details
- ISSN :
- 15882926 and 13886150
- Volume :
- 130
- Database :
- OpenAIRE
- Journal :
- Journal of Thermal Analysis and Calorimetry
- Accession number :
- edsair.doi...........8f7c3316e8ae89f28016bfb66fe45464
- Full Text :
- https://doi.org/10.1007/s10973-017-6389-y