1,3-Dipalmitoyl-2-oleoylglycerol

CAS: 2190-25-2

Ref. 3D-CAA19025

Produktinformation

• Name: 1,3-Dipalmitoyl-2-oleoylglycerol
• Synonyme: 1,3-Dihexadecanoyl-2-(9i-octadecenoyl)glycerol, 1,3-Dipalmito-2-olein, 1,3-Dipalmitoyl-2-olein, 1,3-Dipalmitoyl-2-oleoylglycerin, 1,3-bis(hexadecanoyloxy)propan-2-yl (9Z)-octadec-9-enoate, 1-Palmito-2-oleo-3-palmitin, 2-Oleo-1,3-dipalmitin, 2-Oleodipalmitin, 2-Oleoyl-1,3-dipalmitin, 2-Oleoyl-1,3-dipalmitoylglycerin, 2-Oleoyl-1,3-dipalmitoylglycerol, 9-Octadecenoic acid (9Z)-, 2-[(1-oxohexadecyl)oxy]-1-[[(1-oxohexadecyl)oxy]methyl]ethyl ester, 9-Octadecenoic acid (Z)-, 2-[(1-oxohexadecyl)oxy]-1-[[(1-oxohexadecyl)oxy]methyl]ethyl ester, Glycerin-1-palmitate-2-oleate-3-palmitate, Glycerol 1,3-dipalmitate 2-oleate, Glyceryl 2-oleate-1,3-dipalmitate, Olein, 1,3-dipalmito-2-, Palmitin, 2-oleo-1,3-di-, Pop-Tg, Triglyceride POP,sn
• CAS: 2190-25-2

Beschreibung

1,3-Dipalmitoyl-2-oleoylglycerol is a metastable lipid that belongs to the group of analogs. It has been detected in food composition and as an extractable lipid from animal tissues. 1,3-Dipalmitoyl-2-oleoylglycerol is a mixture of β-unsaturated ketones that are extracted from fats and oils, although it can also be synthesized. The synthesis of this compound can be achieved by reacting an acyl chain with a β-unsaturated ketone in the presence of a base catalyst, such as sodium methoxide or potassium t-butoxide. This reaction requires activation energies which depend on the type of activation method used. Chemical ionization (CI) requires less activation energy than liquid chromatography/mass spectrometry (LC/MS). Optimal reaction conditions for CI involve using a flow rate of 1 mL/min, gas temperature at 150°C, and collision

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 833.36 g/mol
• Formel: C₅₃H₁₀₀O₆
• Reinheit: Min. 95%