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Merck
CN

860833P

Avanti

C6(6-azido) GalCer

Avanti Research - A Croda Brand

别名:

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

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关于此项目

经验公式(希尔记法):
C30H56 N4O8
化学文摘社编号:
分子量:
600.79
UNSPSC Code:
12352211
NACRES:
NA.25
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产品名称

C6(6-azido) GalCer, Avanti Research - A Croda Brand 860833P, powder

InChI

1S/C30H56N4O8/c1-2-3-4-5-6-7-8-9-10-11-12-13-15-18-24(36)23(33-26(37)19-16-14-17-20-32-34-31)22-41-30-29(40)28(39)27(38)25(21-35)42-30/h15,18,23-25,27-30,35-36,38-40H,2-14,16-17,19-22H2,1H3,(H,33,37)/b18-15+/t23-,24+,25+,27-,28-,29+,30+/m0/s1

InChI key

XAHHWMVRWITDCA-QLCMGMRNSA-N

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

assay

>99% (TLC)

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

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

存储类别

11 - Combustible Solids

flash_point_f

No data available

flash_point_c

No data available

法规信息

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分析证书(COA)

Lot/Batch Number

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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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