Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

860843P

Avanti

18:0(2S-OH) Sulfo GalCer

Avanti Research™ - A Croda Brand 860843P, powder

Synonym(s):

3-O-sulfo-D-galactosyl-β1-1′-N-[2"(S)-hydroxystearoyl]-D-erythro-sphingosine (ammonium salt), (synthetic)

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C42H84N2O12S
CAS Number:
2260670-28-6
Molecular Weight:
841.19
UNSPSC Code:
12352211
NACRES:
NA.25

form

powder

packaging

pkg of 1 × 1 mg (860843P-1mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 860843P

lipid type

sphingolipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

[H][C@](/C=C/CCCCCCCCCCCCC)(O)[C@@]([H])(NC([C@@H](O)CCCCCCCCCCCCCCCC)=O)CO[C@H](O1)[C@H](O)[C@@H](OS([O-])(=O)=O)[C@H]([C@H]1CO)O.[NH4+]

General description

18:0(2S-OH) Sulfo GalCer, also known as 3-O-sulfo-D-galactosyl-β1-1′-N-[2"(S)-hydroxystearyl]-D-erythro-sphingosine, is a sulfatide derived from 18:0(2S-OH) GalCer via esterification of a sulfate group to 3-hydroxyl of the galactose moiety. It is a vital constituent of the membranous myelin sheath.

Biochem/physiol Actions

Sulfatides or sulfo-galactosylceramide (S-GalCer) plays a vital role in protein trafficking, signal transduction and neuronal cell differentiation. Elevated levels of S-GalCer in lysosomes due to arylsulfatase A (ASA) deficiency leads to the development of metachromatic leukodystrophy in humans.

Packaging

5 mL Amber Glass Screw Cap Vial (860843P-1mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class

11 - Combustible Solids

flash_point_f

No data available

flash_point_c

No data available

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

Analysis of complex lipidomes
Medical Applications of Mass Spectrometry, 116(2), 223-249 (2008)
Analysis of complex lipidomes
Medical Applications of Mass Spectrometry, 116(2), 223-249 (2008)
R Lüllmann-Rauch et al.
Histochemistry and cell biology, 116(2), 161-169 (2001-10-31)
The inherited deficiency of arylsulfatase A (ASA) causes lysosomal accumulation of sulfoglycolipids (mainly sulfo-galactosylceramide, S-GalCer ) and leads to metachromatic leukodystrophy in humans. Among visceral organs, kidneys are particularly affected. In the present study, the regional distribution and temporal development

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