Journal of Pharmaceutical and Biomedical Analysis 2014-09-01

Detection by HPLC and structural characterization by NMR and MS of a natural deuterium isotopologue of ulipristal acetate.

Zoltán Béni, Judit Orgoványi, János Kóti, Csaba Sánta, János Horváth, Sándor Mahó, Csaba Szántay

Index: J. Pharm. Biomed. Anal. 98 , 279-86, (2014)

Full Text: HTML

Abstract

Herein we discuss the structure elucidation of an unknown peak detected by HPLC in the active pharmaceutical ingredient ulipristal acetate during analytical method development. An extensive chromatographic, MS and NMR spectroscopic study gave the surprising result that the detected component is the natural-abundance mono-deuterium isotopologue of the API. To the best of our knowledge this is the first example where such a mono-deuterium isotopologue could be resolved from its mother component by HPLC and structurally fully characterized by NMR and MS. The reason for this separation could be rationalized in terms of some special structural features of the molecule. Copyright © 2014 Elsevier B.V. All rights reserved.

Related Compounds

Structure Name/CAS No. Articles
Formic Acid Structure Formic Acid
CAS:64-18-6
Chloroform Structure Chloroform
CAS:67-66-3
Acetonitrile Structure Acetonitrile
CAS:75-05-8
Formic acid ammonium salt Structure Formic acid ammonium salt
CAS:540-69-2
Triethylamine Phosphate Structure Triethylamine Phosphate
CAS:35365-94-7