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About This Item
Empirical Formula (Hill Notation):
C9H6O2
CAS Number:
Molecular Weight:
146.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
Indan-1,2-dione, 97%
InChI
1S/C9H6O2/c10-8-5-6-3-1-2-4-7(6)9(8)11/h1-4H,5H2
SMILES string
O=C1Cc2ccccc2C1=O
InChI key
WFFZGYRTVIPBFN-UHFFFAOYSA-N
assay
97%
form
solid
mp
117-124 °C
functional group
ketone
Quality Level
Related Categories
Application
Indan-1,2-dione is a latent fingerprint reagent widely used in forensic chemistry. It can also be used to synthesize polycyclic arene and heteroarene systems containing five membered rings.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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A Combined Experimental and Theoretical Study of the Ammonium Bifluoride Catalyzed Regioselective Synthesis of Quinoxalines and Pyrido[2,3-b]pyrazines.
Lassagne F, et al.
Synthesis, 47, 2680-2689 (2015)
Chemical development of latent fingerprints: 1, 2-indanedione has come of age.
Wiesner S, et al.
Journal of Forensic Sciences, 46(5), 1082-1084 (2001)
Patrick Fritz et al.
Forensic science international, 257, 20-28 (2015-08-19)
Dimethylaminocinnamaldehyde was re-evaluated as a wet contact reagent for the treatment of latent fingermarks on porous substrates. A new formulation (consisting of 0.028 g p-dimethylaminocinnamaldehyde, 0.84 mL glacial acetic acid, 6.2 mL ethyl acetate and 0.993 L 40-60 °C petroleum
Optimisation and evaluation of 1,2-indanedione for use as a fingermark reagent and its application to real samples.
Wallace-Kunkel C, et al.
Forensic Science International, 168(1), 14-26 (2007)
Niko Nicolasora et al.
Forensic science international, 288, 266-277 (2018-05-25)
This paper contains details of work carried out to identify the most effective processing conditions for the optimized 1,2-indandione/zn formulation developed for use under UK conditions. Using direct measurements of fluorescence taken from test spots of amino acids and eccrine
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