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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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Gangliosides in Health and Disease (2018)
Pediatric Neurology (2013)
Matrix-free mass spectrometry imaging of mouse brain tissue sections on silicon nanopost arrays
Fincher JA, et al.
The Journal of Comparative Neurology (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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