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Hydrogen-bonding interactions in the 4-aminobenzoic acid salt of atenolol monohydrate

Lou, Benyong (author)
Luleå tekniska universitet,Medicinsk vetenskap
Boström, Dan (author)
Umeå universitet,Energiteknik och termisk processkemi,Energy Technology and Thermal Process Chemistry, Umeå University
Velaga, Sitaram (author)
Luleå tekniska universitet,Medicinsk vetenskap
 (creator_code:org_t)
International Union of Crystallography, 2007
2007
English.
In: Acta Crystallographica Section C. - : International Union of Crystallography. - 0108-2701 .- 1600-5759. ; 63:12, s. 714-716
  • Journal article (peer-reviewed)
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  • Atenolol {or 4-[2-hydroxy-3-(isopropylamino)propoxy]phenyl-acetamide} crystallizes with 4-aminobenzoic acid to give the salt {3-[4-(aminocarbonylmethyl)phenoxy]-2-hydroxypropy1}- isopropylammonium 4-aminobenzoate monohydrate, C14H23- N2O3*C7H6NO2-*H2O. In the crystal structure, the water molecule, the carboxylate group of 4-aminobenzoate, and the hydroxy and ether O atoms of atenolol form a supramolecular R33(11) heterosynthon. Three other types of supramolecular synthons link the asymmetric unit into a two-dimensional structure.

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