2-Pyridylethylamine
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| Names | |
|---|---|
|  IUPAC name
 2-Pyridin-2-ylethanamine[1]  | |
| Identifiers | |
|  2706-56-1  | |
| 3D model (Jmol) |  Interactive image Interactive image  | 
| 111208 | |
| ChEBI |  CHEBI:147599  | 
| ChEMBL |  ChEMBL32813  | 
| ChemSpider |  68424  | 
| ECHA InfoCard | 100.018.450 | 
| EC Number | 220-295-1 | 
| 1197 | |
| MeSH | 2-(2-Aminoethyl)pyridine | 
| PubChem | 75919 | 
| UN number | 2735 | 
 
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  | |
| Properties | |
| C7H10N2 | |
| Molar mass | 122.17 g·mol−1 | 
| Density | 1.021 g cm−3 | 
| Boiling point | 93 °C; 199 °F; 366 K at 1.6 kPa | 
| log P | -0.11 | 
|   Refractive index (nD)  | 
1.536 | 
| Hazards | |
| GHS pictograms |  ![]()  | 
| GHS signal word | WARNING | 
| H315, H319, H335 | |
| P261, P305+351+338 | |
|   EU classification (DSD)  | 
  | 
| R-phrases | R36/37/38 | 
| S-phrases | S26, S36 | 
| NFPA 704 | |
| Flash point | 100 °C (212 °F; 373 K) | 
|   Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).  | |
|   | |
| Infobox references | |
2-Pyridylethylamine is a histamine agonist which is selective for the H1 subtype.[2]
References
- ↑ CID 75919 from PubChem
 - ↑  Flynn SB, Gristwood RW, Owen DA (January 1979). "Differentiation of the roles of histamine H1- and H2-receptors in the mediation of the effects of histamine in the isolated working heart of the guinea-pig". Br. J. Pharmacol. 65 (1): 127–37. doi:10.1111/j.1476-5381.1979.tb17341.x. PMC 1668480
. PMID 32943. 
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