1,8-Diazafluoren-9-one
| Names | |
|---|---|
| Preferred IUPAC name
9H-Cyclopenta[1,2-b:4,3-b′]dipyridin-9-one | |
| Other names
DFO 9H-1,8-Diazafluoren-9-one 9H-Pyrido[3′,2′:3,4]cyclopenta[1,2-b]pyridin-9-one | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C11H6N2O | |
| Molar mass | 182.182 g·mol−1 |
| Appearance | Yellow powder |
| Melting point | 229–233 °C (444–451 °F; 502–506 K) |
| Hazards | |
| GHS labelling: | |
| NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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.