1,2-Indandione
1,3-Indandione is an organic compound with the molecular formula C9H6O2. Chemically, it is a vicinal diketone on an indane framework.
![]() | |
| Names | |
|---|---|
Other names
| |
| Identifiers | |
| |
3D model (JSmol) |
|
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.153.649 |
| EC Number |
|
PubChem CID |
|
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C9H6O2 | |
| Molar mass | 146.145 g·mol−1 |
| Melting point | 117–124 °C (243–255 °F; 390–397 K) |
| Boiling point | 273.8 °C (524.8 °F; 547.0 K) |
| log P | 0.32 |
| Hazards | |
| GHS classification and labelling: | |
![]() ![]() | |
| Danger | |
| H302, H315, H317, H318, H335 | |
| P261, P264, P270, P271, P272, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P330, P332+P313, P333+P313, P362, P363, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
1,2-Indandione is used in the first stage of forensic identification of latent fingerprints. It is particularly useful for paper, and for items printed with thermal inks such as receipts. Amino acids left behind by the human hand may be developed into fingerprints by the use of it; the results, photographed with a special filter under a strong yellow-green fluorescent or green laser. It is usually the first method employed in a sequential analysis aimed at the production of evidence of a grade suitable for use in the courtroom. [1]
References
- Sequential Processing 2010 : 01 : History of Indanedione. Sequential Processing of Documents For Fingerprints. NFSTC. Retrieved August 2, 2013.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.


