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216879

6-Aminopyridine-3-carboxylic acid

Name: 6-Aminopyridine-3-carboxylic acid
Brand: ALDRICH

97%

Synonym(s):

6-Aminonicotinic acid

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About This Item

Empirical Formula (Hill Notation):

C₆H₆N₂O₂

CAS Number:

3167-49-5

Molecular Weight:

138.12

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24852983

EC Number:

221-630-4

Beilstein/REAXYS Number:

115992

MDL number:

MFCD00006326

Assay:

97%

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Properties

Quality Level

100

assay

97%

mp

>300 °C (lit.)

functional group

carboxylic acid

SMILES string

Nc1ccc(cn1)C(O)=O

InChI

1S/C6H6N2O2/c7-5-2-1-4(3-8-5)6(9)10/h1-3H,(H2,7,8)(H,9,10)

InChI key

ZCIFWRHIEBXBOY-UHFFFAOYSA-N

Description

General description

Electrosynthesis of 6-aminopyridine-3-carboxylic acid (6-aminonicotinic acid) by electrochemical reduction of 2-amino-5-bromo and 2-amino-5-chloropyridine in the presence of CO₂at silver electrode has been reported.

Application

6-Aminopyridine-3-carboxylic acid (6-Aminonicotinic acid) was used in the preparation of resin-bound 2-aminoazine.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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A three-component solid-phase synthesis of 3-aminoimidazo [1, 2-a] azines.

Blackburn C.

Tetrahedron Letters, 39(31), 5469-5472 (1998)

Two genetically distinct pathways for transcriptional regulation of anaerobic gene expression in Salmonella typhimurium.

D J Jamieson et al.

Journal of bacteriology, 168(1), 389-397 (1986-10-01)

Expression of the tripeptide permease gene tppB is anaerobically induced. This induction is independent of the fnr (oxrA) gene product, which is known to be required for the anaerobic induction of several respiratory enzymes. We isolated, characterized, and mapped mutations

Metabolism and excretion of (S)-6-(3-cyclopentyl-2-(4-trifluoromethyl)-1H-imidazol-1-yl)propanamido)nicotinic acid (PF-04991532), a hepatoselective glucokinase activator, in humans: confirmation of the MIST potential noted in first-in-Human metabolite scouting studies.

Raman Sharma et al.

Xenobiotica; the fate of foreign compounds in biological systems, 49(12), 1447-1457 (2019-02-13)

1. The absorption, metabolism, and excretion of a single oral 450-mg dose of [14C]-(S)-6-(3-cyclopentyl-2-(4-trifluoromethyl)-1H-imidazol-1-yl)propanamido)nicotinic acid (PF-04991532), a hepatoselective glucokinase activator, was investigated in humans. Mass balance was achieved with ∼94.6% of the administered dose recovered in urine and feces. The

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Global Trade Item Number

SKU	GTIN
216879-5G	04061833070802
216879-1G	04061838774675