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A77989

Sigma-Aldrich

2-Aminopyridine

≥99%

Synonym(s):

o-Aminopyridine, 2-AP, 2-Pyridinamine, 2-Pyridylamine

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About This Item

Empirical Formula (Hill Notation):
C5H6N2
CAS Number:
Molecular Weight:
94.11
Beilstein/REAXYS Number:
105785
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥99%

form

crystals

bp

204-210 °C (lit.)

mp

54-58 °C (lit.)

SMILES string

Nc1ccccn1

InChI

1S/C5H6N2/c6-5-3-1-2-4-7-5/h1-4H,(H2,6,7)

InChI key

ICSNLGPSRYBMBD-UHFFFAOYSA-N

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General description

2-Aminopyridine is a basic building block of several heterocyclic compounds and Schiff bases.

Application

2-Aminopyridine (2AP) is a derivatizing agent which can be used as a fluorescent label for oligosaccharide detection, chromatographic separation, fluorometric or mass spectrometric analysis.
2AP and its derivatives are good candidates for antimicrobial, anticorrosion and molecular sensing applications.

pictograms

CorrosionSkull and crossbones

signalword

Danger

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_germany

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


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Aminopyrimidine derivatives as inhibitors for corrosion of 1018 carbon steel in nitric acid solution.
Abdallah M, et al.
Corrosion Science, 48(7), 1639-1654 (2006)
Application of 2-aminopyridine fluorescence labeling in the analysis of in vivo and in vitro metabolism of dextran sulfate sodium by size-exclusion high-performance liquid chromatography.
Araki Y, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 753(2), 209-215 (2001)
De facto molecular weight distributions of glucans by size-exclusion chromatography combined with mass/molar-detection of fluorescence labeled terminal hemiacetals.
Praznik W and Huber A
Journal of Chromatography. B, Biomedical Applications, 824(1-2), 295-307 (2005)
Structure analyses of oligosaccharides by tagging of the reducing end sugars with a fluorescent compound.
Hase S, et al.
Biochemical and Biophysical Research Communications, 85(1), 257-263 (1978)
Assignment and quantification of 2-aminopyridine derivatized oligosaccharide isomers coeluted on reversed-phase HPLC/MS by MS n spectral library.
Takegawa Y, et al.
Analytical Chemistry, 76(24), 7294-7303 (2004)

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