Skip to Content
Merck
All Photos(4)

Key Documents

G1639

Sigma-Aldrich

D-(+)-Galactosamine hydrochloride

BioReagent, suitable for cell culture

Synonym(s):

2-Amino-2-deoxy-D-galactopyranose hydrochloride, D-Chondrosamine hydrochloride

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C6H13NO5 · HCl
CAS Number:
Molecular Weight:
215.63
Beilstein:
3697825
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.75

biological source

fish cartilage (shark)

Quality Level

product line

BioReagent

Assay

≥99%

technique(s)

cell culture | mammalian: suitable

impurities

Glucosamine, essentially free

solubility

water: 50 mg/mL, clear to very slightly hazy, colorless to very faintly yellow

shipped in

ambient

storage temp.

room temp

SMILES string

Cl.N[C@@H](C=O)[C@@H](O)[C@@H](O)[C@H](O)CO

InChI

1S/C6H13NO5.ClH/c7-3(1-8)5(11)6(12)4(10)2-9;/h1,3-6,9-12H,2,7H2;1H/t3-,4+,5+,6-;/m0./s1

InChI key

CBOJBBMQJBVCMW-NQZVPSPJSA-N

Looking for similar products? Visit Product Comparison Guide

Application

D-(+)-Galactosamine hydrochloride has been used to:
  • induce livery injury
  • inflammatory liver injury
  • acute liver failure (ALF) in mice

Biochem/physiol Actions

Galactosamine (D-GalN) is synthesized from galactose and is potential hepatotoxic agent. D-GalN in combination with lipopolysaccharide leads to the development of lethal liver injury and hepatic failure. It sensitizes cells to the toxic effects of the cytokine in particular the tumor necrosis factor(TNF).

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

Already Own This Product?

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

Visit the Document Library

Yao Wang et al.
Journal of inflammation research, 14, 1473-1485 (2021-04-23)
The glycolysis pathway of M1 macrophages is a key factor affecting the inflammatory response. The aim of this article is to investigate the role of histone deacetylase 6 (HDAC6) in the M1 macrophage glycolysis pathway during acute liver failure (ALF).
GABA, gamma-Aminobutyric Acid, Protects Against Severe Liver Injury
Hata T, et al.
The Journal of Surgical Research, 236, 172-183 (2019)
Voluntary distance running prevents TNF-mediated liver injury in mice through alterations of the intrahepatic immune milieu
Huber Y, et al.
Cell Death & Disease, 8(6), e2893-e2893 (2017)
D-galactosamine lethality model: scope and limitations
Silverstein R
Journal of endotoxin research, 10(3), 147-162 (2004)
The protective effect of the natural compound hesperetin against fulminant hepatitis in vivo and in vitro
Bai X, et al.
British Journal of Pharmacology, 174(1), 41-56 (2017)

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