Artigo Revisado por pares

Comparison of Solid-State 13 C NMR Spectroscopy and Powder X-ray Diffraction for Analyzing Mixtures of Polymorphs of Neotame

1999; American Chemical Society; Volume: 71; Issue: 16 Linguagem: Inglês

10.1021/ac9902446

ISSN

1520-6882

Autores

Brian E. Padden, Mark T. Zell, Zedong Dong, Stephen A. Schroeder, David Grant, Eric J. Munson,

Tópico(s)

NMR spectroscopy and applications

Resumo

Polymorphism is defined as the ability of a compound to adopt two or more conformations and/or arrangements in its crystalline state. Polymorphism and pseudopolymorphism (i.e., a change in solvation state) are important because the different crystal forms of a compound can have different physical properties, such as density, melting point, and solubility. Powder X-ray diffraction is currently the most common method for determining the existence of polymorphism in crystalline organic compounds. Solid-state 13C NMR spectroscopy has emerged as another powerful analytical technique for determining polymorphism. Both solid-state 13C NMR spectroscopy and powder X-ray diffraction have been used to analyze mixtures of the solid forms of neotame. Neotame, N-(3,3-dimethylbutyl)-l-aspartyl-l-phenylalanine methyl ester, is a new high-potency sweetener that exists in multiple solid forms. The most stable form of neotame under ambient conditions in the presence of moisture is a monohydrate. Altering the crystallization and drying conditions can generate mixtures of solid forms of neotame. A systematic study has been performed to observe the conversion under vacuum of the monohydrate to a mixture of forms and then reconversion to the monohydrate upon exposure to moisture under ambient conditions. No significant changes were observed in the powder X-ray diffraction patterns during part of the reconversion process, suggesting that no change in form had occurred. The solid-state 13C NMR spectra, however, indicated the presence of many forms of neotame during the reconversion. One possible reason that solid-state 13C NMR spectroscopy detected the changes in forms and powder X-ray diffraction did not is that the conformation of the neotame molecules changes between forms but the unit cell parameters do not change significantly.

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