| Weight | 568.924 g/mol |
|---|---|
| Formula | C35H68O5 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 32 |
1,2-Dipalmitoyl-sn-glycerol (30334-71-5)
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- Sigma-Aldrich - 1,2-Dipalmitoyl-sn-glycerol33.20 - 96.30 USD
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- Acyl migration in 1,2-dipalmitoyl-sn-glycerol (Chemistry and Physics of Lipids, 1990)
- Atomic resolution structure analysis of polymorph crystal of a triacylglycerol: 1,2-dipalmitoyl-3-myristoyl-sn-glycerol (Journal of Lipid Research, 2001)
- Single crystal structure of a mixed-chain triacylglycerol: 1,2-dipalmitoyl-3-acetyl-sn-glycerol. (Proceedings of the National Academy of Sciences of the United States of America, 1992)
- Binary Phase Behavior of 1,3-Dipalmitoyl-2-oleoyl-sn-glycerol and 1,2-Dioleoyl-3-palmitoyl-rac-glycerol (Journal of the American Oil Chemists' Society, 2007)
- Polymorphic forms of 1,2-dipalmitoyl-sn-glycerol: a combined X-ray and electron diffraction study (Chemistry and Physics of Lipids, 1988)
- The binary phase behavior of 1, 3-dipalmitoyl-2-stearoyl-sn-glycerol and 1, 2-dipalmitoyl-3-stearoyl-sn-glycerol (Chemistry and Physics of Lipids, 2009)
-
Predict GHS Hazards for Any Chemical in silico.
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SMILESCCCCCCCCCCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCCCCCCCCC
-
InChIKeyJEJLGIQLPYYGEE-UHFFFAOYSA-N
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Synthesis
palmitic acid
+
Reactant
(Ester from carboxilic acid(SN2))
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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1,2-Dipalmitoyl-sn-glycerol
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