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A78209

Sigma-Aldrich

3-Aminopyridine

99%

Synonym(s):

3-Pyridinamine

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About This Item

Empirical Formula (Hill Notation):
C5H6N2
CAS Number:
462-08-8
Molecular Weight:
94.11
Beilstein/REAXYS Number:
105692
EC Number:
207-322-2
MDL number:
MFCD00006400
UNSPSC Code:
12352100
PubChem Substance ID:
24891284
NACRES:
NA.22

assay

99%

form

flakes

bp

248 °C (lit.)

mp

60-63 °C (lit.)

SMILES string

Nc1cccnc1

InChI

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

InChI key

CUYKNJBYIJFRCU-UHFFFAOYSA-N

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pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

190.4 °F - closed cup

flash_point_c

88 °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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Chao Fang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 71(4), 1588-1593 (2008-07-22)
Our algorithm [B. Tian, G. Wu, G. Liu, J. Chem. Phys. 87 (1987) 7300] is introduced to obtain the temporal bond polarizabilities of 2- and 3-aminopyridine from their Raman intensities, which supply fruitful electronic information of the nonresonant Raman excited
Elizabeta Sauer et al.
Antimicrobial agents and chemotherapy, 48(12), 4532-4541 (2004-11-25)
The utilization pathway for the uptake of NAD and nicotinamide riboside was previously characterized for Haemophilus influenzae. We now report on the cellular location, topology, and substrate specificity of PnuC. pnuC of H. influenzae is only distantly related to pnuC
Effects of chronic, intrauterine organic and inorganic mercury intoxication on the epileptogenicity of developing rat.
B Barna et al.
Central European journal of public health, 8 Suppl, 73-75 (2000-08-16)
B Barna et al.
Acta biologica Hungarica, 50(1-3), 257-267 (1999-11-26)
The effect of GYKI 52466, a selective, non-competitive antagonist of the AMPA glutamate receptor subtype was investigated on the development, expression and propagation of 3-aminopyridine-induced cortical ictal activity, both in the primary and secondary focus. In one group of animals
Nitric oxide synthase inhibitor facilitates aminopyridine induced neocortical seizure.
B Boda et al.
Neurobiology (Budapest, Hungary), 4(1-2), 103-104 (1996-01-01)
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