The design of chemical compounds for development of latent fingerprints is
explored computationally. Our main findings are: (a) We show why past attem
pts to improve the widely used ninhydrin gave relatively small improvements
(referring to color only). The optical transition is connected with a "tra
nsition core" and therefore is influenced little by substitution on the aro
matic rings. (b) We propose new analogues of ninhydrin with a significant p
otential such as thiono derivatives.