| Literature DB >> 7175471 |
J Almog, A Hirshfeld, J T Klug.
Abstract
In an attempt to design new reagents for the chemical development of latent fingerprints, a number of ninhydrin analogues were synthesized and their reactions with latent fingerprints on paper were studied. The ring-fused and substituted ninhydrins developed latent fingerprints with a sensitivity similar to that of ninhydrin. The most promising of the group was 2,2-dihydroxybenz[f]indane-1,3-dione, which developed latent fingerprints as dark green images with excellent resolution.Entities:
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Year: 1982 PMID: 7175471
Source DB: PubMed Journal: J Forensic Sci ISSN: 0022-1198 Impact factor: 1.832