L9378
N-Lignoceroyl-DL-dihydrosphingosine
~98%
Synonym(s):
N-Tetracosanoyl-DL-dihydrosphingosine
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About This Item
Empirical Formula (Hill Notation):
C42H85NO3
CAS Number:
Molecular Weight:
652.13
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
Assay
~98%
form
solid
lipid type
sphingolipids
shipped in
ambient
storage temp.
−20°C
SMILES string
CCCCCCCCCCCCCCCCCCCCCCCC(=O)N[C@H](CO)[C@H](O)CCCCCCCCCCCCCCC
InChI
1S/C42H85NO3/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-26-28-30-32-34-36-38-42(46)43-40(39-44)41(45)37-35-33-31-29-27-25-16-14-12-10-8-6-4-2/h40-41,44-45H,3-39H2,1-2H3,(H,43,46)/t40-,41-/m1/s1
InChI key
BPLYVSYSBPLDOA-GYOJGHLZSA-N
Application
N-Lignoceroyl-DL-dihydrosphingosine is a racemic mixture of D and L- N-lignoceroyl-dihydrosphingosine that may be used to evaluate enantomer separation and detection technologies for dihydroceramide lipids.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
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Mototeru Yamane
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 783(1), 181-190 (2002-11-27)
I have developed a simple method which enabled simultaneous analysis of ceramides in the subcellular fractions from cultured cells by HPLC-thermospray mass spectrometry. The HPLC-thermospray mass spectra from ceramide standards were characterized by the high intensity of the MNa(+) and
A E Cremesti et al.
Lipids, 35(9), 937-945 (2000-10-12)
Ceramides are key compounds in the metabolism of sphingolipids and are emerging as important second messengers for various cellular processes including cell cycle arrest, differentiation, senescence, apoptosis, and others. Because of their important biological functions, exact analysis of their molecular
M Yano et al.
Journal of lipid research, 39(10), 2091-2098 (1998-10-27)
A method was developed for quantitative analysis of molecular species of ceramide (N-acyl-sphingosine) and dihydroceramide (N-acyl sphinganine) by high performance liquid chromatography (HPLC). Various N-acyl chain-containing ceramides or dihydroceramides were semi-synthesized as standard materials and allowed to react with anthroyl
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