Oxydipropane-3,1,2-triyl tetralaurate

Base Information

• Chemical Name: Oxydipropane-3,1,2-triyl tetralaurate
• CAS No.: 57012-88-1
• Molecular Formula: C54H102 O9
• Molecular Weight: 895.398
• European Community (EC) Number: 260-513-2
• DSSTox Substance ID: DTXSID30972504
• Nikkaji Number: J106.335I
• Mol file: 57012-88-1.mol

Synonyms:57012-88-1;Oxydipropane-3,1,2-triyl tetralaurate;EINECS 260-513-2;Diglycerin tetralaurate;DTXSID30972504;C54H102O9;C54-H102-O9;Oxydi(propane-3,1,2-triyl) tetradodecanoate

Chemical Property of Oxydipropane-3,1,2-triyl tetralaurate

Chemical Property:

• Vapor Pressure: 2.83E-27mmHg at 25°C
• Boiling Point: 824°Cat760mmHg
• Flash Point: 306.1°C
• PSA: 114.43000
• Density: 0.951g/cm³
• LogP: 15.59660
• XLogP3: 20.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 54
• Exact Mass: 894.75238483
• Heavy Atom Count: 63
• Complexity: 939

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCC(=O)OCC(COCC(COC(=O)CCCCCCCCCCC)OC(=O)CCCCCCCCCCC)OC(=O)CCCCCCCCCCC

Technology Process of Oxydipropane-3,1,2-triyl tetralaurate

There total 2 articles about Oxydipropane-3,1,2-triyl tetralaurate 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:

lauric acid (143-07-7) + diglycerol (627-82-7) → bis-(2,3-bis-lauroyloxy-propyl)-ether (57012-88-1)

Guidance literature:

at 160 - 170 ℃; nicht rein erhalten;

Reference yield:

→ bis-(2,3-bis-lauroyloxy-propyl)-ether (57012-88-1)

Guidance literature:

entspr. Diglycerol, Laurinsaeure-isopropenylaether;

upstream raw materials:

lauric acid

diglycerol