Skip to Content
Merck
CN
All Photos(2)

Key Documents

Safety Information

A77989

Sigma-Aldrich

2-Aminopyridine

≥99%

Synonym(s):

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

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C5H6N2
CAS Number:
Molecular Weight:
94.11
Beilstein:
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

Looking for similar products? Visit Product Comparison Guide

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

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1A

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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)
Glycan analysis by modern instrumental methods.
Pabst M and Altmann F
Proteomics, 11(4), 631-643 (2011)
2-Aminopyridine derivative as fluorescence `On?Off?molecular switch for selective detection of Fe3+/Hg2+.
Koner RR, et al.
Tetrahedron Letters, 53(18), 2302-2307 (2012)

Protocols

Explore mass spectrometry analysis of glycans for glycomic & glycoproteomic neutral & acidic glycan analysis. See a general mass spec glycan analysis procedure.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service