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dc.contributor.author
Brusau, Elena Virginia  
dc.contributor.author
Camí, Gerardo Enrique  
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Narda, Griselda Edith  
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Cuffini, Silvia Lucia  
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Ayala, A. P.  
dc.contributor.author
Ellena, J.  
dc.date.available
2024-08-12T11:57:32Z  
dc.date.issued
2008-01  
dc.identifier.citation
Brusau, Elena Virginia; Camí, Gerardo Enrique; Narda, Griselda Edith; Cuffini, Silvia Lucia; Ayala, A. P.; et al.; Synthesis and Characterization of a New Mebendazole Salt: Mebendazole Hydrochloride; John Wiley & Sons; Journal of Pharmaceutical Sciences; 97; 1; 1-2008; 542-552  
dc.identifier.issn
0022-3549  
dc.identifier.uri
http://hdl.handle.net/11336/242252  
dc.description.abstract
Mebendazole hydrochloride [(5‐benzoyl‐1H‐benzimidazole‐2‐yl)‐carbamic acid methyl ester hydrochloride, MBZ·HCl], a new stable salt of mebendazole (MBZ), has been synthesized and characterized. It can easily be obtained from recrystallization of forms A, B, or C of MBZ in diverse solvents with the addition of hydrochloric acid solution. Crystallographic data reveals that the particular conformation adopted by the carbamic group contributes to the stability of the network. The crystal packing is stabilized by the presence of three N–H…Cl intermolecular interactions that form chains along the b axis. The XRD analyses of the three crystalline habits found in the crystallization process (square‐based pyramids, pseudohexagonal plates, and prismatic) show equivalent diffraction patterns. The vibrational behavior is consistent with crystal structure. The most important functional groups show shifts to lower or higher frequencies in relation to the MBZ polymorphs. The thermal study on MBZ·HCl indicates that the compound is stable up to 160°C approximately. Decomposition occurs in four steps. In the first step the HCl group is eliminated, and after that the remaining MBZ polymorph A decomposes in three steps, as happens with polymorphs B and C.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
John Wiley & Sons  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Mebendazole hydrochloride  
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Polymorphism  
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Salt formation  
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Otras Ciencias Químicas  
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Ciencias Químicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Synthesis and Characterization of a New Mebendazole Salt: Mebendazole Hydrochloride  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2024-08-08T15:50:18Z  
dc.journal.volume
97  
dc.journal.number
1  
dc.journal.pagination
542-552  
dc.journal.pais
Estados Unidos  
dc.description.fil
Fil: Brusau, Elena Virginia. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia; Argentina  
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Fil: Camí, Gerardo Enrique. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia; Argentina  
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Fil: Narda, Griselda Edith. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Investigaciones en Tecnología Química. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Investigaciones en Tecnología Química; Argentina  
dc.description.fil
Fil: Cuffini, Silvia Lucia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; Argentina  
dc.description.fil
Fil: Ayala, A. P.. Universidade Federal do Ceara; Brasil  
dc.description.fil
Fil: Ellena, J.. Universidade de Sao Paulo; Brasil  
dc.journal.title
Journal of Pharmaceutical Sciences  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://linkinghub.elsevier.com/retrieve/pii/S0022354916324625  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/jps.21164