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Chemical compound From Wikipedia, the free encyclopedia
3-Aminopyridine is an aminopyridine. It is a colorless solid.[1]
Names | |
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Preferred IUPAC name
Pyridin-3-amine | |
Other names
3-Pyridinamine; 3-Pyridylamine | |
Identifiers | |
3D model (JSmol) |
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ChemSpider | |
ECHA InfoCard | 100.006.658 |
PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C5H6N2 | |
Molar mass | 94.117 g·mol−1 |
Appearance | [citation needed] |
Melting point | 65 °C (149 °F; 338 K) |
Boiling point | 248 °C (478 °F; 521 K) |
Soluble[vague] | |
Solubility in alcohol and benzene | Soluble[vague] |
Hazards | |
Flash point | 124 °C (255 °F; 397 K) |
628 °C (1,162 °F; 901 K) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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3-Aminopyridine is prepared by heating nicotinamide with sodium hypobromite (Hofmann rearrangement), which is in turn prepared in situ by the reaction of sodium hydroxide and bromine at 70 °C.[2]
It can be used in the synthesis of organic ligand 3-pyridylnicotinamide. Troxipide is another synthesis that uses 3-AP.
The acute toxicity is indicated by the LD50 = 178 mg/kg (quail, oral).[1]
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