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      2-Amino-5-bromo­pyridinium hydrogen succinate

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          Abstract

          In the title compound, C5H6BrN2 +·C4H5O4 −, the pyridine N atom of the 2-amino-5-bromo­pyridine mol­ecule is protonated. The protonated N atom and the amino group are linked via N—H⋯O hydrogen bonds to the carboxyl­ate O atoms of the singly deprotonated succinate anion. The hydrogen succinate anions are linked via O—H⋯O hydrogen bonds. A weak inter­molecular C—H⋯O hydrogen bond is also observed.

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          Author and article information

          Affiliations
          [a ]X-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, 11800 USM, Penang, Malaysia
          Author notes
          Correspondence e-mail: hkfun@ 123456usm.my
          [‡]

          Thomson Reuters ResearcherID: A-3561-2009.

          Journal
          Acta Crystallogr Sect E Struct Rep Online
          Acta Cryst. E
          Acta Crystallographica Section E: Structure Reports Online
          International Union of Crystallography
          1600-5368
          01 March 2010
          27 February 2010
          27 February 2010
          : 66
          : Pt 3 ( publisher-idID: e100300 )
          : o689-o690
          2983627
          21580432
          is2526
          10.1107/S1600536810006495
          ACSEBH S1600536810006495
          © Hemamalini and Fun 2010

          This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

          Categories
          Organic Papers

          Materials characterization

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