1,2-Dimyristoyl-3-palmitoyl-rac-glycerol

Base Information

• Chemical Name: 1,2-Dimyristoyl-3-palmitoyl-rac-glycerol
• CAS No.: 60138-13-8
• Molecular Formula: C47H90O6
• Molecular Weight: 751.21
• DSSTox Substance ID: DTXSID90394142
• Nikkaji Number: J603.426H
• Mol file: 60138-13-8.mol

Synonyms:1,2-Dimyristoyl-3-palmitoyl-rac-glycerol;60138-13-8;1,2-Ditetradecanoyl-3-hexadecanoyl-rac-glycerol;115144-39-3;2,3-di(tetradecanoyloxy)propyl hexadecanoate;rac-1,2-dimyristoyl-3-palmitoylglycerol;1,2-Myristin-3-Palmitin;SCHEMBL2734702;DTXSID90394142;Glycerol 1,2-dimyristate 3-palmitate;PD126725;1,2-Dimyristoyl-3-palmitoyl-rac-glycerol, ~99%;rac-1,2-di tetradecanoyl-3-hexadecanoyl-glycerol;TG 14:0_14:0_16:0

Chemical Property of 1,2-Dimyristoyl-3-palmitoyl-rac-glycerol

Chemical Property:

• Melting Point: 47.8 °C
• Boiling Point: 722.6±27.0 °C(Predicted)
• PSA: 78.90000
• Density: 0.921±0.06 g/cm3(Predicted)
• LogP: 14.86810
• Storage Temp.: −20°C
• XLogP3: 19.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 46
• Exact Mass: 750.67374059
• Heavy Atom Count: 53
• Complexity: 783

Purity/Quality:

97% ^*data from raw suppliers

1,2-Dimyristoyl-3-palmitoyl-rac-glycerol ^*data from reagent suppliers

Safty Information:

• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCC
• Description: 1,2-Dimyristoyl-3-palmitoyl-rac-glycerol is a triacylglycerol that contains myristic acid and the sn-1 and sn-2 positions and palmitic acid at the sn-3 position. It has been found in butterfat.

Technology Process of 1,2-Dimyristoyl-3-palmitoyl-rac-glycerol

There total 4 articles about 1,2-Dimyristoyl-3-palmitoyl-rac-glycerol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

tetradecanoyl chloride (112-64-1) → 1,2-bis-myristoyloxy-3-palmitoyloxy-propane (60138-13-8,115144-39-3)

Guidance literature:

With quinoline;

Reference yield:

n-tetradecanoic acid (544-63-8) → 1,2-bis-myristoyloxy-3-palmitoyloxy-propane (60138-13-8,115144-39-3)

Guidance literature:

Multi-step reaction with 2 steps

2: quinoline

With quinoline;

Reference yield:

tetradecanoyl chloride (112-64-1) → 1,2-bis-myristoyloxy-3-palmitoyloxy-propane (60138-13-8,115144-39-3)

Guidance literature:

With pyridine; chloroform;

DOI:10.1039/jr9580003186

upstream raw materials:

rac-1-monopalmitoylglycerol

tetradecanoyl chloride

n-tetradecanoic acid