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Merck

A77989

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-988-4
Beilstein/REAXYS Number:
105785
MDL number:
Assay:
≥99%
Form:
crystals
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InChI key

ICSNLGPSRYBMBD-UHFFFAOYSA-N

InChI

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

SMILES string

Nc1ccccn1

assay

≥99%

form

crystals

bp

204-210 °C (lit.)

mp

54-58 °C (lit.)

Quality Level

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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

Skull and crossbonesCorrosion

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

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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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)
A combined strategy for glycan profiling: a model study with pyridylaminated oligosaccharides.
Kamekawa N, et al.
Journal of Biochemistry, 140(3), 337-347 (2006)
Inhibitive effect of some Schiff bases on corrosion of aluminium in hydrochloric acid solutions.
Bansiwal A, et al.
Corrosion Engineering, Science and Technology, 35(4), 301-303 (2000)
Synthesis, characterization and antibacterial properties of symmetric 1, 1??ferrocene derived Schiff?base ligands and their Co (II), Cu (II), Ni (II) and Zn (II) chelates.
Chohan ZH and Praveen M
Applied Organometallic Chemistry, 14(7), 376-382 (2000)
Antimicrobial activity studies of the binuclear metal complexes derived from tridentate Schiff base ligands.
Tumer M, et al.
Transition Metal Chemistry, 24(4), 414-420 (1999)

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