1-Oleoyl-2-palmitoyl-sn-glycerol

Base Information

Chemical Name:1-Oleoyl-2-palmitoyl-sn-glycerol
CAS No.:64199-61-7
Molecular Formula:C₃₇H₇₀O₅
Molecular Weight:594.96
Hs Code.:
DSSTox Substance ID:DTXSID901169820
Nikkaji Number:J2.296.558A
Wikidata:Q27145315
Metabolomics Workbench ID:5791

Synonyms:1-oleoyl-2-palmitoyl-sn-glycerol;DG(18:1(9Z)/16:0/0:0);1-(9Z-octadecenoyl)-2-hexadecanoyl-sn-glycerol;(2S)-2-(hexadecanoyloxy)-3-hydroxypropyl (9Z)-octadec-9-enoate;LMGL02010005;1-oleoyl-2-palmitoyl-glycerol;SCHEMBL7918252;CHEBI:75447;1-oleoyl,2-palmitoyl-sn-glycerol;Diacylglycerol(18:1n9/16:0);Diacylglycerol(18:1w9/16:0);DTXSID901169820;[(2S)-2-hexadecanoyloxy-3-hydroxypropyl] (Z)-octadec-9-enoate;1-O-Oleoyl-2-O-palmitoyl-L-glycerol;1-O-oleoyl-2-O-palmitoyl-sn-glycerol;DAG(18:1n9/16:0);DAG(18:1w9/16:0);64199-61-7;DG(18:1n9/16:0);DG(18:1w9/16:0);Q27145315;DG (18:1(9Z)/16:0/0:0);(2S)-3-Hydroxy-2-[(1-oxohexadecyl)oxy]propyl (9Z)-9-octadecenoate

Suppliers and Price of 1-Oleoyl-2-palmitoyl-sn-glycerol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 1-Oleoyl-2-palmitoyl-sn-glycerol

Chemical Property:

PSA：72.83000
LogP:10.95250
XLogP3:14.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:35
Exact Mass:594.52232533
Heavy Atom Count:42
Complexity:603

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Lipids -> Ambiguous Lipids
Canonical SMILES:CCCCCCCCCCCCCCCC(=O)OC(CO)COC(=O)CCCCCCCC=CCCCCCCCC
Isomeric SMILES:CCCCCCCCCCCCCCCC(=O)O[C@@H](CO)COC(=O)CCCCCCC/C=C\CCCCCCCC

Technology Process of 1-Oleoyl-2-palmitoyl-sn-glycerol

There total 2 articles about 1-Oleoyl-2-palmitoyl-sn-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: 69.0%

: 945247-22-3
3-O-benzyl-1-O-oleoyl-2-O-palmitoyl-sn-glycerol

: 64199-61-7,38991-91-2
1-O-oleoyl-2-O-palmitoyl-sn-glycerol

Guidance literature:: With boron trichloride; In dichloromethane; at -78 ℃; for 0.75h;
DOI:10.1039/b702551c

Reference yield:

: 142924-97-8
1-O-(9z)-octadenoyl-3-benzylglycerol

: 64199-61-7,38991-91-2
1-O-oleoyl-2-O-palmitoyl-sn-glycerol

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / DCC; DMAP / CH₂Cl₂ / 12 h / 20 °C

2: 69 percent / boron trichloride / CH₂Cl₂ / 0.75 h / -78 °C

With dmap; boron trichloride; dicyclohexyl-carbodiimide; In dichloromethane;
DOI:10.1039/b702551c