8-Hydroxyquinoline
| Names | |
|---|---|
| Preferred IUPAC name
Quinolin-8-ol | |
| Other names
1-Azanaphthalene-8-ol, Fennosan H 30, Hydroxybenzopyridine, Oxybenzopyridine, Oxychinolin, Oxyquinoline, Phenopyridine, Quinophenol, Oxine, 8-Quinolinol | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.005.193 |
| KEGG | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C9H7NO | |
| Molar mass | 145.16 g/mol |
| Appearance | White crystalline powder |
| Density | 1.034 g/cm3 |
| Melting point | 76 °C (169 °F; 349 K) |
| Boiling point | 276 °C (529 °F; 549 K) |
| Pharmacology | |
| G01AC30 (WHO) A01AB07 (WHO) D08AH03 (WHO) R02AA14 (WHO) | |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H301, H317, H318, H360D, H410 | |
| P202, P273, P280, P301+P310, P302+P352, P305+P351+P338 | |
| 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).
Infobox references | |
8-Hydroxyquinoline (also known as oxine) is an organic compound derived from the heterocycle quinoline. A colorless solid, its conjugate base is a chelating agent, which is used for the quantitative determination of metal ions.
In aqueous solution 8-hydroxyquinoline has a pKa value of ca. 9.9 It reacts with metal ions, losing the proton and forming 8-hydroxyquinolinato-chelate complexes.
The aluminium complex, is a common component of organic light-emitting diodes (OLEDs). Substituents on the quinoline ring affect the luminescence properties.
In its photo-induced excited-state, 8-hydroxyquinoline converts to zwitterionic isomers, in which the hydrogen atom is transferred from oxygen to nitrogen.