Names | |
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Preferred IUPAC name
2,2-Dihydroxy-1H-indene-1,3(2H)-dione | |
Other names
2,2-Dihydroxyindane-1,3-dione
1,2,3-Indantrione hydrate | |
Identifiers | |
3D model (JSmol)
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ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.006.926 |
EC Number |
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PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C9H6O4 | |
Molar mass | 178.143 g·mol−1 |
Appearance | White solid |
Density | 0.862 g/cm3 |
Melting point | 250 °C (482 °F; 523 K) (decomposes) |
20 g L−1[1] | |
Hazards | |
GHS labelling: | |
Warning | |
H302, H315, H319, H335 | |
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Safety data sheet (SDS) | External MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Ninhydrin (2,2-dihydroxyindane-1,3-dione) is an organic compound with the formula C6H4(CO)2C(OH)2. It is used to detect ammonia and amines. Upon reaction with these amines, ninhydrin gets converted into deep blue or purple derivatives, which are called Ruhemann's purple. Ninhydrin is most commonly used to detect fingerprints in forensic cases, as the terminal amines of lysine residues in peptides and proteins sloughed off in fingerprints react with ninhydrin.[2][3]
Ninhydrin is a white solid that is soluble in ethanol and acetone.[1] Ninhydrin can be considered as the hydrate of indane-1,2,3-trione.