Published in

American Chemical Society, Crystal Growth and Design, 2(14), p. 783-791, 2013

DOI: 10.1021/cg401662d

Links

Tools

Export citation

Search in Google Scholar

Furosemide cocrystals : structures, hydrogen bonding, and implications for properties.

Journal article published in 2013 by Bethany I. Harriss, Liana Vella-Zarb, Claire Wilson ORCID, Ivana Radosavljevic Evans
This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Green circle
Preprint: archiving allowed
  • Must obtain written permission from Editor
  • Must not violate ACS ethical Guidelines
Upload
Orange circle
Postprint: archiving restricted
  • Must obtain written permission from Editor
  • Must not violate ACS ethical Guidelines
Upload
Red circle
Published version: archiving forbidden
Policy details
Data provided by SHERPA/RoMEO

Abstract

Four new crystal structures of pharmaceutical molecule furosemide with GRAS coformers are reported and correlated with the known pharmacologically relevant properties of these materials. Furosemide carboxylic acid oxygen donor−coformer aromatic nitrogen acceptor is the dominant synthon, leading to the key intermolecular interactions in the cocrystals studied.