Abstract
The crystal structure of α-(N-benzoxazoline-2-one) acetic acid is studied in the following forms: hydrate, solvate with formic acid, organic monoethanolammonium salt (NН2(CH2)2OH) in two polymorphs produced by minor changes in the crystallization temperature, and also its ethylenediammonium salt (NН2(CH2)2NH2) in the 2:1 ratio, where amino groups participate in the deprotonation of two molecules of α-(N-benzoxazoline-2-one) acetic acid. Weak intermolecular hydrogen and dative bonds in the crystals consisting of different molecules are analyzed.
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