In the title monohydrate salt of ambroxol (AMB) with theophylline-7-acetic acid (TAA), protonation of the secondary amino group of AMB takes place. An hydrogen bond is established between the protonated N atom and an O atom of the carboxylate anion, the same atom as is involved in an N-HO interaction with the aromatic amino group of the cation. The other O atom of the carboxylate anion participates in an hydrogen bond with a symmetry-related salt molecule, giving rise to a dimeric arrangement. The water molecule is linked to a carbonyl O atom of TAA and the aromatic amino group of AMB, and connects the salt molecules in the crystal at the level of the OH group of AMB.

Ambroxol theophylline-7-acetate salt monohydrate

BETTINETTI, GIAMPIERO;SORRENTI, MILENA LILLINA;
1998-01-01

Abstract

In the title monohydrate salt of ambroxol (AMB) with theophylline-7-acetic acid (TAA), protonation of the secondary amino group of AMB takes place. An hydrogen bond is established between the protonated N atom and an O atom of the carboxylate anion, the same atom as is involved in an N-HO interaction with the aromatic amino group of the cation. The other O atom of the carboxylate anion participates in an hydrogen bond with a symmetry-related salt molecule, giving rise to a dimeric arrangement. The water molecule is linked to a carbonyl O atom of TAA and the aromatic amino group of AMB, and connects the salt molecules in the crystal at the level of the OH group of AMB.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/485214
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