4-Amino­pyridinium 5-carb­oxy­penta­noate monohydrate

In the title hydrated salt, C(5)H(7)N(2) (+)·C(6)H(9)O(4) (−)·H(2)O, the carb­oxy H atom is disordered over two positions with equal occupancy. In the crystal, O atoms of the 5-carb­oxy­penta­noate anion link the 4-amino­pyridinium cations and water mol­ecules into a three-dimensional network via N—...

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Detalles Bibliográficos
Autores principales: Raj, S. Alfred Cecil, Sinthiya, A., Varghese, Babu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393984/
https://www.ncbi.nlm.nih.gov/pubmed/22798849
http://dx.doi.org/10.1107/S1600536812027638
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author Raj, S. Alfred Cecil
Sinthiya, A.
Varghese, Babu
author_facet Raj, S. Alfred Cecil
Sinthiya, A.
Varghese, Babu
author_sort Raj, S. Alfred Cecil
collection PubMed
description In the title hydrated salt, C(5)H(7)N(2) (+)·C(6)H(9)O(4) (−)·H(2)O, the carb­oxy H atom is disordered over two positions with equal occupancy. In the crystal, O atoms of the 5-carb­oxy­penta­noate anion link the 4-amino­pyridinium cations and water mol­ecules into a three-dimensional network via N—H⋯O hydrogen bonds. The crystal structure is further consolidated by O—H⋯O hydrogen bonds involving the anion and the solvent water mol­ecule.
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spelling pubmed-33939842012-07-13 4-Amino­pyridinium 5-carb­oxy­penta­noate monohydrate Raj, S. Alfred Cecil Sinthiya, A. Varghese, Babu Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title hydrated salt, C(5)H(7)N(2) (+)·C(6)H(9)O(4) (−)·H(2)O, the carb­oxy H atom is disordered over two positions with equal occupancy. In the crystal, O atoms of the 5-carb­oxy­penta­noate anion link the 4-amino­pyridinium cations and water mol­ecules into a three-dimensional network via N—H⋯O hydrogen bonds. The crystal structure is further consolidated by O—H⋯O hydrogen bonds involving the anion and the solvent water mol­ecule. International Union of Crystallography 2012-06-23 /pmc/articles/PMC3393984/ /pubmed/22798849 http://dx.doi.org/10.1107/S1600536812027638 Text en © Raj et al. 2012 http://creativecommons.org/licenses/by/2.0/uk/ 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.
spellingShingle Organic Papers
Raj, S. Alfred Cecil
Sinthiya, A.
Varghese, Babu
4-Amino­pyridinium 5-carb­oxy­penta­noate monohydrate
title 4-Amino­pyridinium 5-carb­oxy­penta­noate monohydrate
title_full 4-Amino­pyridinium 5-carb­oxy­penta­noate monohydrate
title_fullStr 4-Amino­pyridinium 5-carb­oxy­penta­noate monohydrate
title_full_unstemmed 4-Amino­pyridinium 5-carb­oxy­penta­noate monohydrate
title_short 4-Amino­pyridinium 5-carb­oxy­penta­noate monohydrate
title_sort 4-amino­pyridinium 5-carb­oxy­penta­noate monohydrate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393984/
https://www.ncbi.nlm.nih.gov/pubmed/22798849
http://dx.doi.org/10.1107/S1600536812027638
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