Phenanthridine
| Names | |
|---|---|
| Preferred IUPAC name
Phenanthridine | |
| Other names
Benzo[c]quinoline
6-Phenanthridine 3,4-Benzoquinoline 9-Azaphenanthrene 3,4-Benzoisioquinoline 5-Azaphenanthrene CCRIS 1234 | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.005.396 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C13H9N | |
| Molar mass | 179.222 g·mol−1 |
| Appearance | colorless solid |
| Density | 1.341 g/cm3 |
| Melting point | 104–107 °C |
| Boiling point | 349 °C at 1.025 hPa |
| almost insoluble (7.7 μg/mL at pH 7.4) | |
| Vapor pressure | 0.0000208 mmHg |
| Acidity (pKa) | 4.61 |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H301, H315, H318, H335 | |
| P261, P264, P264+P265, P270, P271, P280, P301+P316, P302+P352, P304+P340, P305+P354+P338, P317, P319, P321, P330, P332+P317, P362+P364, P403+P233, P405, P501 | |
| Flash point | 100 °C (closed cup) |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose) |
oral, rat: 100 mg/kg (acute toxic) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Phenanthridine is a nitrogen heterocyclic compound with the formula C13H9N. It is a colorless solid, although impure samples can be brownish. It is a precursor to DNA-binding fluorescent dyes through intercalation. Examples of such dyes are ethidium bromide and propidium iodide. Phenanthridine was discovered by Amé Pictet and H. J. Ankersmit in 1891.