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860840P

Avanti

C18(2R-OH) Galactosyl(β) Ceramide

Avanti Research™ - A Croda Brand 860840P, powder

Synonym(s):

D-galactosyl-β1-1′-N-[2′′(R)-hydroxystearoyl]-D-erythro-sphingosine

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About This Item

Empirical Formula (Hill Notation):
C42H81NO9
CAS Number:
35823-62-2
Molecular Weight:
744.09
UNSPSC Code:
12352211
NACRES:
NA.25

form

powder

packaging

pkg of 1 × 5 mg (860840P-5mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 860840P

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](O)[C@H]([C@H]1CO)O

General description

Galactosyl ceramide is a complex glycosphingolipid, which is a major component of the myelin sheath. It consists of a single galactose residue linked to ceramide.

Application

C18(2R-OH) Galactosyl(β) Ceramide has been used as a standard to study unsaturated glycosphingolipids using the shotgun approach. It has also been used as a lipid standard for matrix-assisted laser desorption ionization (MALDI) analysis.

Biochem/physiol Actions

Galactosyl ceramide is essential for normal myelin function and stability.

Packaging

5 mL Amber Glass Screw Cap Vial (860840P-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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’.

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Matrix-free mass spectrometry imaging of mouse brain tissue sections on silicon nanopost arrays
Fincher JA, et al.
The Journal of Comparative Neurology (2018)
Pediatric Neurology (2013)
Gangliosides in Health and Disease (2018)
Divalent cation-mediated interaction between cerebroside sulfate and cerebrosides: an investigation of the effect of structural variations of lipids by electrospray ionization mass spectrometry
Koshy KM, et al.
Biophysical Journal, 77(1), 306-318 (1999)
Structural analysis of unsaturated glycosphingolipids using shotgun ozone-induced dissociation mass spectrometry
Barrientos RC, et al.
Journal of the American Society For Mass Spectrometry, 28(11), 2330-2343 (2017)
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