Journal of Pharmacy and Pharmacology p. 441 - 443 (1979)
Update date:2022-08-31
Topics:
Lebelle
Vilim
Wilson
A fluorescent impurity in ampicillin has been isolated and identified as 2-hydroxy-3-phenyl-pyrazine. The product is formed under acidic conditions similar to those employed in some fluorometric assay procedures. The mechanism of the reaction is proposed to involve cyclization by condensation of the penilloaldehyde of ampicillin. The structure was confirmed by independent synthesis.
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