D6783
DL-Dihydrosphingosine
≥98%, synthetic
Synonym(s):
1,3-Dihydroxy-2-aminooctadecane, DL-1,3-Dihydroxy-2-aminooctadecane
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About This Item
Recommended Products
biological source
synthetic
Assay
≥98%
form
solid
storage temp.
−20°C
SMILES string
CCCCCCCCCCCCCCCC(O)C(N)CO
InChI
1S/C18H39NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(21)17(19)16-20/h17-18,20-21H,2-16,19H2,1H3
InChI key
OTKJDMGTUTTYMP-UHFFFAOYSA-N
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General description
Dihydrosphingosine is a crucial constituent of the skin lipid barrier, which guards the body from excessive water loss.
Application
DL-Dihydrosphingosine has been used to initiate heat stress signals in Saccharomyces cerevisiae.
Biochem/physiol Actions
Biosynthetic precursor of sphingosine.
Other Notes
Mixture of erythro and threo isomers. Content given on label.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Sphingolipids Are Potential Heat Stress Signals inSaccharomyces
The Journal of Biological Chemistry, 272(48), 30196-30200 (1997)
Phytosphingosine, sphingosine and dihydrosphingosine ceramides in model skin lipid membranes: permeability and biophysics
Biochimica et Biophysica Acta - Biomembranes, 1859(5), 824-834 (2017)
Bioorganic & medicinal chemistry, 4(7), 1035-1043 (1996-07-01)
We have developed a simple picomole (low nanogram) scale HPLC scheme which can separate all eight isomers of sphingosine and dihydrosphingosine thus leading to the identification of their relative and absolute configurations. The amino group of the sample is derivatized
Blood, 93(2), 686-693 (1999-01-13)
In the present study, we investigated the mechanism by which sphingosine and its analogues, dihydrosphingosine and phytosphingosine, inhibit polymorphonuclear leukocyte (PMN) phagocytosis of IgG-opsonized erythrocytes (EIgG) and inhibit ERK1 and ERK2 phosphorylation. We used antibodies that recognized the phosphorylated forms
Journal of lipid research, 58(7), 1428-1438 (2017-05-19)
Ceramides (Cers) and complex sphingolipids with defined acyl chain lengths play important roles in numerous cell processes. Six Cer synthase (CerS) isoenzymes (CerS1-6) are the key enzymes responsible for the production of the diversity of molecular species. In this study
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