Reagents for the Chemical Development of Latent Fingerprints: Synthesis and Properties of Some Ninhydrin Analogues

Joseph Almog, Amiram Hirshfeld

Journal of Forensic Sciences · 1982 · 63 citations · 8 references

Concepts

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.

References

8