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经验公式（希尔记法）:
C42H81 NO8
化学文摘社编号:
分子量:
728.09
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.25
产品名称
C18 Galactosyl(β) Ceramide (d18:1/18:0), Avanti Research™ - A Croda Brand 860844P, powder
SMILES string
[H][C@](/C=C/CCCCCCCCCCCCC)(O)[C@@]([H])(NC(CCCCCCCCCCCCCCCCC)=O)CO[C@H](O1)[C@H](O)[C@@H](O)[C@H]([C@H]1CO)O
InChI
1S/C42H81NO8/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-38(46)43-35(34-50-42-41(49)40(48)39(47)37(33-44)51-42)36(45)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2/h29,31,35-37,39-42,44-45,47-49H,3-28,30,32-34H2,1-2H3,(H,43,46)/b31-29+
InChI key
YMYQEDCYNANIPI-OWWNRXNESA-N
assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 5 mg (860844P-5mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand 860844P
lipid type
sphingolipids
shipped in
dry ice
storage temp.
−20°C
Application
C18 Galactosyl(β) Ceramide (d18:1/18:0) or D-galactosyl- β -1,1′-N-stearoyl-D-erythro-sphingosine has been used as a cerebroside standard in glycolipid isomer analysis using ultra-high resolution ion mobility spectrometry separations.
Packaging
5 mL Amber Glass Screw Cap Vial (860844P-5mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
No data available
flash_point_c
No data available
法规信息
涉药品监管产品
此项目有
Roza Wojcik et al.
International journal of molecular sciences, 18(1) (2017-01-21)
Understanding the biological roles and mechanisms of lipids and glycolipids is challenging due to the vast number of possible isomers that may exist. Mass spectrometry (MS) measurements are currently the dominant approach for studying and providing detailed information on lipid
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