Journal of Forensic Sciences · 1992 · 29 citations · 11 references
PharmacyMedicinal ChemistryDrug DiscoveryImpurity ProfilingOrganic ChemistryChemical FingerprintingToxicological Drug ScreeningChemical Reagent DevelopmentCompound Fingerprinting
Abstract Ninhydrin derivatives bearing sulfur-containing groups at position 5 exhibit excellent properties as fluorogenic fingerprint reagents on paper. Their sensitivity markedly exceeds that of ninhydrin and even that of 5-methoxy ninhydrin. Preliminary experiments indicate it as equal to or better than 1–8-diazafluorene-9-one (DFO). One member of this group, 5-methylthio ninhydrin, has been recently declared an operational fingerprint developer in our laboratory.
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