scholarly journals Comparison of Detection Effectiveness by Physical Developer, Oil Red O and Nile Red Methods as Reagent for Latent Fingerprints on Porous Surfaces

2015 ◽  
Vol 29 (2) ◽  
pp. 287-315
Author(s):  
Lee Gill Rack ◽  
Chae,Jong-Min
2013 ◽  
Vol 230 (1-3) ◽  
pp. 74-80 ◽  
Author(s):  
Karl Braasch ◽  
Mackenzie de la Hunty ◽  
Janina Deppe ◽  
Xanthe Spindler ◽  
Antonio A. Cantu ◽  
...  

2019 ◽  
Author(s):  
Clara M. Agapie ◽  
Melissa Sampson ◽  
William Gee

The work describes a new chemical means of visualising latent fingerprints (fingermarks) using tropolone. Tropolone reacts with amino acids within the fingermark residue to form adducts that absorb UV radiation. These adducts provide useful contrast on highly-fluorescent prous surfaces will illuminated with UV radiation. The conjugated seven-membered ring of the tropolone adduct can be reacted further diazonium salts, which is demonstrated here with formation of two dyes. The methodology is extremely rapid, occurring in minutes with mild heating, and can be applied before ninhydrin in a chemical detection sequence. <br>


Author(s):  
Somaya Madkour ◽  
Abeer sheta ◽  
Fatma Badr El Dine ◽  
Yasser Elwakeel ◽  
Nermine AbdAllah

2000 ◽  
Vol 45 (4) ◽  
pp. 14768J ◽  
Author(s):  
Claude Roux ◽  
Chris Jones ◽  
Milutin Lennard ◽  
Milutin Stoilovic

2020 ◽  
Vol 14 ◽  
pp. 100383
Author(s):  
Marcela de S. Brandão ◽  
Joilson R. Jesus ◽  
Alyne R. de Araújo ◽  
Juarez G. de Carvalho ◽  
Miguel Peixoto ◽  
...  

2019 ◽  
Author(s):  
Clara M. Agapie ◽  
Melissa Sampson ◽  
William Gee

The work describes a new chemical means of visualising latent fingerprints (fingermarks) using tropolone. Tropolone reacts with amino acids within the fingermark residue to form adducts that absorb UV radiation. These adducts provide useful contrast on highly-fluorescent prous surfaces will illuminated with UV radiation. The conjugated seven-membered ring of the tropolone adduct can be reacted further diazonium salts, which is demonstrated here with formation of two dyes. The methodology is extremely rapid, occurring in minutes with mild heating, and can be applied before ninhydrin in a chemical detection sequence. <br>


2001 ◽  
Vol 79 (11) ◽  
pp. 1632-1654 ◽  
Author(s):  
Richard R Hark ◽  
Diane B Hauze ◽  
Olga Petrovskaia ◽  
Madeleine M Joullié

Ninhydrin is an essential tool in the analysis of amino acids, peptides, and proteins, and the preferred reagent for the detection of latent fingerprints on porous surfaces. The goal of this investigation was to prepare ninhydrin analogs with enhanced chromogenic and fluorogenic properties. Target compounds included structures with extended conjugation and (or) with the presence of sulfur-containing moieties. We have devised general convergent routes for novel heterocyclic and aryl-substituted ninhydrin analogs for use as reagents for amino acid detection.Key words: ninhydrin analogs, synthesis, ketals, Suzuki cross-coupling reactions, Stille cross-coupling reactions.


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