| Weight | 648.903 g/mol |
|---|---|
| Formula | C35H69O8P |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 34 |
Dipalmitoyl (7091-44-3)
Score:
#1552 in Physics
,
#3692 in Biology
,
#4644 in Chemistry
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- Effect of small molecules on the dipalmitoyl lecithin liposomal bilayer: III. Phase transition in lipid bilayer (The Journal of Membrane Biology, 1977)
- Deuterium magnetic resonance study of the gel and liquid crystalline phases of dipalmitoyl phosphatidylcholine (Biophysical Journal, 1979)
- Ternary Phase Diagram of Dipalmitoyl-PC/Dilauroyl-PC/Cholesterol: Nanoscopic Domain Formation Driven by Cholesterol (Biophysical Journal, 2001)
- Conformation and motion of the choline head group in bilayers of dipalmitoyl-3-sn-phosphatidylcholine. (Biochemistry, 1975)
- A Fourier transform infrared spectroscopic study of the molecular interaction of cholesterol with 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (Biochimica et Biophysica Acta, 1980)
- Characterization of the pretransition in 1,2-dipalmitoyl-sn-glycero-3-phosphocholine by Fourier transform infrared spectroscopy. (Biochemistry, 1980)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)O)OC(=O)CCCCCCCCCCCCCCC
-
InChIKeyPORPENFLTBBHSG-UHFFFAOYSA-N
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Synthesis
palmitic acid
+
Reactant
(Ester from carboxilic acid(SN2))
Palmitoyl chloride
+
Reactant
(O-acylation)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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