Misplaced Pages

2-Pyridylethylamine

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
2-Pyridylethylamine
Kekulé, skeletal formula of 2-pyridylethylamine
Names
Preferred IUPAC name 2-(Pyridin-2-yl)ethan-1-amine
Identifiers
CAS Number
3D model (JSmol)
Beilstein Reference 111208
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.018.450 Edit this at Wikidata
EC Number
  • 220-295-1
IUPHAR/BPS
MeSH 2-(2-Aminoethyl)pyridine
PubChem CID
UNII
UN number 2735
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C7H10N2/c8-5-4-7-3-1-2-6-9-7/h1-3,6H,4-5,8H2Key: XPQIPUZPSLAZDV-UHFFFAOYSA-N
  • InChI=1/C7H10N2/c8-5-4-7-3-1-2-6-9-7/h1-3,6H,4-5,8H2Key: XPQIPUZPSLAZDV-UHFFFAOYAY
SMILES
  • NCCc1ccccn1
  • NCCC1=CC=CC=N1
Properties
Chemical formula C7H10N2
Molar mass 122.171 g·mol
Density 1.021 g cm
Boiling point 93 °C; 199 °F; 366 K at 1.6 kPa
log P -0.11
Refractive index (nD) 1.536
Hazards
GHS labelling:
Pictograms GHS07: Exclamation mark
Signal word Warning
Hazard statements H315, H319, H335
Precautionary statements P261, P305+P351+P338
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1 1 0
Flash point 100 °C (212 °F; 373 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

2-Pyridylethylamine is a histamine agonist which is selective for the H1 subtype.

References

  1. 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.
Histamine receptor modulators
H1
Agonists
Antagonists
H2
Agonists
Antagonists
H3
Agonists
Antagonists
H4
Agonists
Antagonists
See also
Receptor/signaling modulators
Monoamine metabolism modulators
Monoamine reuptake inhibitors
Stub icon

This article about an amine is a stub. You can help Misplaced Pages by expanding it.

Stub icon

This article about a heterocyclic compound is a stub. You can help Misplaced Pages by expanding it.

Categories: