| Identification | Back Directory | [Name]
N-palMitoyl-D-erythro-sphinganine | [CAS]
5966-29-0 | [Synonyms]
C16 Dihydroceramide (d18:0/16:0)
N-palMitoyl-D-erythro-sphinganine
C16-dihydro-Ceramide (N-palmitoyl)
(2S,3R)-2-hexadecanoylaminooctadecane-1,3-diol
Hexadecanamide, N-[(1S,2R)-2-hydroxy-1-(hydroxymethyl)heptadecyl]-
N-PALMITOYL-D-ERYTHRO-SPHINGANINE;C16 DIHYDROCERAMIDE (D18:0/16:0) | [Molecular Formula]
C34H69NO3 | [MDL Number]
MFCD02094233 | [MOL File]
5966-29-0.mol | [Molecular Weight]
539.92 |
| Chemical Properties | Back Directory | [Boiling point ]
675.7±45.0 °C(Predicted) | [density ]
0.912±0.06 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
Chloroform:Methanol (5:1): Soluble; DMSO: Soluble; Ethanol: Soluble | [form ]
A solid | [pka]
14.30±0.20(Predicted) |
| Hazard Information | Back Directory | [Uses]
C16 Dihydroceramide (cas# 5966-29-0) is a compound useful in organic synthesis. | [Definition]
ChEBI: N-hexadecanoylsphinganine is a dihydroceramide in which the ceramide N-acyl group is specified as hexadecanoyl (palmitoyl). It has a role as a mouse metabolite. It is a N-acylsphinganine, a Cer(d34:0) and a N-palmitoyl-sphingoid base. It is functionally related to a hexadecanoic acid. | [Biological Activity]
Dihydroceramide acts as a precursor for ceramide synthesis. It has an ability to induce autophagy in the perinuclear region. Dihydroceramide affects autophagic flux and enhances the formation lipid droplets. Accumulation of C16-dihydroceramides might lead to liver injury. |
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