09340
2-Aminopyridine
purum, ≥98.0% (NT)
Synonym(s):
2-AP, 2-Pyridinamine, 2-Pyridylamine
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About This Item
Empirical Formula (Hill Notation):
C5H6N2
CAS Number:
Molecular Weight:
94.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-988-4
Beilstein/REAXYS Number:
105785
MDL number:
Assay:
≥98.0% (NT)
grade
purum
Quality Level
assay
≥98.0% (NT)
bp
204-210 °C (lit.)
mp
54-58 °C (lit.), 54-59 °C
SMILES string
Nc1ccccn1
InChI
1S/C5H6N2/c6-5-3-1-2-4-7-5/h1-4H,(H2,6,7)
InChI key
ICSNLGPSRYBMBD-UHFFFAOYSA-N
Application
Used to label neutral and acidic glycans for fluorescent and UV detection in HPLC. 2-AP has also been used to derivatize sialyloligosaccharides for detection in FAB-MS.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1A
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
197.6 °F - closed cup
flash_point_c
92 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
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Fotini N Lamari et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 793(1), 15-36 (2003-07-26)
Carbohydrates, either alone or as constituents of glycoproteins, proteoglycans and glycolipids, are mediators of several cellular events and (patho)physiological processes. Progress in the "glycome" project is closely related to the analytical tools used to define carbohydrate structure and correlate structure
M Okamoto
Bioscience, biotechnology, and biochemistry, 65(11), 2519-2527 (2002-01-17)
To establish a new protocol for sensitive detection and structural characterization of sialyl oligosaccharides, their sensitivities and structural information from mass spectrometry and tandem mass spectrometry with FAB-, ESI-, and MALDI were evaluated in detail. Among these ionization methods, FAB-MS
Honggen Wang et al.
Journal of the American Chemical Society, 132(38), 13217-13219 (2010-09-09)
A novel and efficient synthesis of pyrido[1,2-a]benzimidazoles through direct intramolecular aromatic C-H amination of N-aryl-2-aminopyridines has been developed. The reaction, cocatalyzed by Cu(OAc)(2) and Fe(NO(3))(3)·9H(2)O, is carried out in DMF under a dioxygen atmosphere. Diversified pyrido[1,2-a]benzimidazoles containing various substitution patterns