1-Stearoyl-2-linoleoyl-sn-glycerol

Base Information

Chemical Name:1-Stearoyl-2-linoleoyl-sn-glycerol
CAS No.:34487-26-8
Molecular Formula:C39H72 O5
Molecular Weight:620.998
Hs Code.:2916190090
DSSTox Substance ID:DTXSID501131538
Nikkaji Number:J161.401K
Wikidata:Q27088818
Metabolomics Workbench ID:5836
ChEMBL ID:CHEMBL1734767
Mol file:34487-26-8.mol

Synonyms:1,2-sn-SLDG;1-stearoyl-2-linoleoyl-sn-glycerol

Suppliers and Price of 1-Stearoyl-2-linoleoyl-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

TRC
1-Stearoyl-2-linoleoyl-sn-glycerol
5mg
$ 180.00

American Custom Chemicals Corporation
1-OCTADECANOYL-2-(9Z,12Z-OCTADECADIENOYL)-SN-GLYCEROL 95.00%
5MG
$ 500.84

Total 4 raw suppliers

Chemical Property of 1-Stearoyl-2-linoleoyl-sn-glycerol

Chemical Property:

Boiling Point:670.2°Cat760mmHg
Flash Point:186.1°C
PSA：72.83000
Density:0.934g/cm³
LogP:11.50870
XLogP3:14.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:36
Exact Mass:620.53797539
Heavy Atom Count:44
Complexity:671

Purity/Quality:

99.3% ^*data from raw suppliers

1-Stearoyl-2-linoleoyl-sn-glycerol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCC=CCC=CCCCCC
Isomeric SMILES:CCCCCCCCCCCCCCCCCC(=O)OC[C@H](CO)OC(=O)CCCCCCC/C=C\C/C=C\CCCCC
Uses 1-Stearoyl-2-linoleoyl-sn-glycerol is used in the study of the influence of platelet-derived growth factor (PDGF) on diacylglycerol phosphorylation in Swiss 3T3 cells. It is also a possible protein kinase C activator.

Technology Process of 1-Stearoyl-2-linoleoyl-sn-glycerol

There total 1 articles about 1-Stearoyl-2-linoleoyl-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: 30.0%

: phosphatidylsphingosine

: 34487-26-8
1-stearoyl-2-linoleoyl-sn-glycerol

: 26993-30-6,26993-39-5
Sphingosine-1-phosphate

Guidance literature:: With phosphate buffer; phospholipase C; 2,6-di-tert-butyl-4-methyl-phenol; In diethyl ether; at 30 ℃; for 4h;
DOI:10.1039/a804770g

Reference yield: 56.0%

: 34487-26-8
1-stearoyl-2-linoleoyl-sn-glycerol

: 42855-00-5
nitroveratryloxycarbonyl chloride

: 1446427-94-6
C₄₉H₈₁NO₁₁

Guidance literature:: 1-stearoyl-2-linoleoyl-sn-glycerol; With pyridine; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 ℃; for 0.05h; Inert atmosphere;

nitroveratryloxycarbonyl chloride; In dichloromethane; at 20 ℃; for 18h; Darkness; Inert atmosphere;
DOI:10.1002/anie.201301716

Reference yield:

: 34487-26-8
1-stearoyl-2-linoleoyl-sn-glycerol

: 816-94-4,18603-43-5
distearoylphosphatidylcholine

Guidance literature:: Multi-step reaction with 2 steps

1: (i) POCl₃, CHCl₃, (ii) /BRN= 3563126/, Py, quinoline

2: H₂ / PtO₂

With hydrogen; platinum(IV) oxide;