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Preferred IUPAC name 9H-Cyclopentadipyridin-9-one | |
Other names
DFO 9H-1,8-Diazafluoren-9-one 9H-Pyridocyclopentapyridin-9-one | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChemSpider | |
PubChem CID | |
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CompTox Dashboard (EPA) | |
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Properties | |
Chemical formula | C11H6N2O |
Molar mass | 182.182 g·mol |
Appearance | Yellow powder |
Melting point | 229–233 °C (444–451 °F; 502–506 K) |
Hazards | |
GHS labelling: | |
Pictograms | |
NFPA 704 (fire diamond) | 2 1 0 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references |
1,8-Diazafluoren-9-one (DFO) is an aromatic ketone first synthesized in 1950. It is used to find fingerprints on porous surfaces. It makes fingerprints glow when they are lit by blue-green light.
DFO reacts with amino acids present in the fingerprint to form highly fluorescent derivatives. Excitation with light at ~470 nm results in emission at ~570 nm.
References
- Lewkowicz, Aneta; Baranowska, Karolina; Bojarski, Piotr; Józefowicz, Marek (2019). "Solvent dependent spectroscopic properties of fingerprint reagent - 1,8-Diazafluoren-9-one". Journal of Molecular Liquids. 285: 754–765. doi:10.1016/j.molliq.2019.04.110. S2CID 149852434.
- ^ Pounds, C. Anthony; Grigg, Ronald; Mongkolaussavaratana, Theeravat (1 January 1990). "The Use of 1,8-Diazafluoren-9-one (DFO) for the Fluorescent Detection of Latent Fingerprints on Paper. A Preliminary Evaluation". Journal of Forensic Sciences. 35 (1): 169–175. doi:10.1520/JFS12813J.
External links
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