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A55306

Sigma-Aldrich

2-(2-Pyridyl)ethylamine

95%

Synonym(s):

2-(2-Aminoethyl)pyridine

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About This Item

Empirical Formula (Hill Notation):
C7H10N2
CAS Number:
2706-56-1
Molecular Weight:
122.17
Beilstein:
111208
EC Number:
220-295-1
MDL number:
MFCD00006367
UNSPSC Code:
12352100
PubChem Substance ID:
24890987
NACRES:
NA.22

Assay

95%

form

liquid

refractive index

n20/D 1.536 (lit.)

bp

92-93 °C/12 mmHg (lit.)

density

1.021 g/mL at 25 °C (lit.)

SMILES string

NCCc1ccccn1

InChI

1S/C7H10N2/c8-5-4-7-3-1-2-6-9-7/h1-3,6H,4-5,8H2

InChI key

XPQIPUZPSLAZDV-UHFFFAOYSA-N

Gene Information

human ... HRH1(3269)

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Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

212.0 °F - closed cup

Flash Point(C)

100 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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E Nakazato et al.
Life sciences, 67(10), 1139-1147 (2000-08-23)
Intrahippocampal administration of the histamine H1 receptor antagonist pyrilamine (3.2-32 ug/ side) but not the histamine H2 receptor antagonist cimetidine (1.0-10 microg/side) increased the number of errors in the working memory task with a three-panel runway setup. The increase in
S Itoh et al.
Journal of the American Chemical Society, 123(45), 11168-11178 (2001-11-08)
Bis(mu-oxo)dinickel(III) complexes supported by a series of bis[2-(2-pyridyl)ethyl]amine ligands have been successfully generated by treating the corresponding bis(mu-hydroxo)dinickel(II) complexes or bis(mu-methoxo)dinickel(II) complex with an equimolar amount of H(2)O(2) in acetone at low temperature. The bis(mu-oxo)dinickel(III) complexes exhibit a characteristic UV-vis
T Ishikawa et al.
The Journal of physiology, 468, 379-400 (1993-08-01)
1. The modulation of whole-cell K+ and Ca2+ currents by stimulation of histamine H1-receptors in freshly isolated single smooth muscle cells from the rabbit coronary artery was characterized using the patch-clamp technique at 35 degrees C. Single-channel K+ currents were
Susanne Mommert et al.
British journal of pharmacology, 177(3), 600-613 (2019-07-23)
Human monocyte-derived M1 macrophages develop in relation to growth factors, bacterial products, and cytokines in a local micro-environment. M1 macrophages produce pro-inflammatory mediators, in particular, oncostatin M (OSM), which is secreted from the cells in response to the active complement
H C Liang et al.
Inorganic chemistry, 39(26), 5884-5894 (2001-02-24)
Copper-dioxygen interactions are of interest due to their importance in biological systems as reversible O2- carriers, oxygenases, or oxidases and also because of their role in industrial and laboratory oxidation processes. Here we report on the kinetics (stopped-flow, -90 to
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