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860833P

Avanti

C6(6-azido) GalCer

Avanti Research™ - A Croda Brand 860833P, powder

Synonym(s):

D-galactosyl-β-1,1′ N-(6"-azidohexanoyl)-D-erythro-sphingosine

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About This Item

Empirical Formula (Hill Notation):
C30H56 N4O8
CAS Number:
2260670-20-8
Molecular Weight:
600.79
UNSPSC Code:
12352211
NACRES:
NA.25

form

powder

packaging

pkg of 1 × 5 mg (860833P-5mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 860833P

lipid type

click reagents

shipped in

dry ice

storage temp.

−20°C

SMILES string

[H][C@](/C=C/CCCCCCCCCCCCC)(O)[C@@]([H])(NC(CCCCCN=[N+]=[N-])=O)CO[C@H](O1)[C@H](O)[C@@H](O)[C@H]([C@H]1CO)O

General description

C6(6-azido) GalCer, also known as D-galactosyl-β-1,1′ N-(6"-azidohexanoyl)-D-erythro-sphingosine is a head group modified lipid comprising an omega-terminal azide. The terminal azide group is involved in a highly specific linking reaction with alkyne-containing reagents, known as ‘click chemistry′, in the presence of a copper (Cu)-containing catalyst. Copper-catalyzed azide−alkyne click chemistry plays a vital role in bioconjugation.

Packaging

5 mL Amber Glass Screw Cap Vial (860833P-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

Flash Point(F)

No data available

Flash Point(C)

No data available

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

860833P-VAR:
860833P-5MG:
860833P-BULK:

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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Stanislav I Presolski et al.
Current protocols in chemical biology, 3(4), 153-162 (2011-01-01)
The copper-catalyzed azide-alkyne cycloaddition reaction is widely used for the connection of molecular entities of all sizes. A protocol is provided here for the process with biomolecules. Ascorbate is used as reducing agent to maintain the required cuprous oxidation state.

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