2000
DOI: 10.1520/jfs14726j
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Reagents for the Chemical Development of Latent Fingerprints: Scope and Limitations of Benzo[f]ninhydrin in Comparison to Ninhydrin

Abstract: Benzo[f]ninhydrin was compared to ninhydrin for fingerprint development on paper. Overall, the performance of ninhydrin on exhibits was slightly better than that of benzo[f]ninhydrin. The significant advantages of the benzo[f]ninhydrain over ninhydrin were the much stronger fluorescence it gave after treatment with zinc salts and a slightly quicker reaction under ambient conditions. This fluorescence is, however, similar to that obtained with other reagents, such as DFO or ninhydrin analogs. These advantages a… Show more

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Cited by 27 publications
(9 citation statements)
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“…Modifications of ninhydrin have been another focus of research, with many analogues produced and evaluated including 5-methylthioninhydrin (Almog et al, 1992), 5-methoxyninhydrin (Lennard, Margot, Stoilovic, & Warrener, 1986), and benzo[f]ninhydrin (Almog et al, 2000). Of all of these analogues, 5-methylthioninhydrin (5MTN) has proved most useful.…”
Section: Amino Acidsmentioning
confidence: 99%
“…Modifications of ninhydrin have been another focus of research, with many analogues produced and evaluated including 5-methylthioninhydrin (Almog et al, 1992), 5-methoxyninhydrin (Lennard, Margot, Stoilovic, & Warrener, 1986), and benzo[f]ninhydrin (Almog et al, 2000). Of all of these analogues, 5-methylthioninhydrin (5MTN) has proved most useful.…”
Section: Amino Acidsmentioning
confidence: 99%
“…Ninhydrin is recognised as the predominant reagent for the visualisation of latent fingermarks on porous surfaces to aid criminal investigations [49][50][51][52]. On reaction with amino acids, ninhydrin (2,2-dihydroxy-1,3-indanedione) forms a non-fluorescent purple product.…”
Section: Ninhydrinmentioning
confidence: 99%
“…The reagent was first synthesised and discovered to react with amino acids in 1910 by Siegfried Ruhemann. A colour change was observed after the reagent contacted his skin, with the formation of a purple compound that was subsequently named "Ruhemann's purple" [49,52]. It took until the mid 1950s before the suggestion was made, by Oden and von Hofsten, that ninhydrin could be used as a means to detect latent fingermarks on porous substrates [7].…”
Section: Ninhydrinmentioning
confidence: 99%
“…Over the past century, many fingerprint development approaches have been studied, including optical, physical, and chemical processes. [7,8] If a latent fingerprint left at a crime scene cannot be developed clearly by a valid method, proper fingerprint analysis and identification will be difficult to achieve. Therefore, latent fingerprint development is crucial to identifying individuals in forensic sciences.…”
Section: Introductionmentioning
confidence: 99%