Glycidyl oleate

Base Information

Chemical Name:Glycidyl oleate
CAS No.:5431-33-4
Molecular Formula:C21H38 O3
Molecular Weight:338.531
Hs Code.:
European Community (EC) Number:226-588-0
NSC Number:13542
UNII:G0I0157S14
DSSTox Substance ID:DTXSID101031637
Nikkaji Number:J34.617I
Wikidata:Q27155965
ChEMBL ID:CHEMBL230967
Mol file:5431-33-4.mol

Synonyms:glycidyl oleate

Suppliers and Price of Glycidyl oleate

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

Usbiological
Glycidyl Oleate
100mg
$ 460.00

TRC
GlycidylOleate
100mg
$ 180.00

American Custom Chemicals Corporation
2,3-EPOXYPROPYL OLEATE 95.00%
5MG
$ 504.45

Total 13 raw suppliers

Chemical Property of Glycidyl oleate

Chemical Property:

Vapor Pressure:1.31E-07mmHg at 25°C
Melting Point:-1 °C
Refractive Index:1.5192 (estimate)
Boiling Point:430.3°Cat760mmHg
Flash Point:163.7°C
PSA：38.83000
Density:0.941g/cm³
LogP:5.96590
Storage Temp.:Refrigerator
Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly) , Methanol (Slightly)
XLogP3:7.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:18
Exact Mass:338.28209507
Heavy Atom Count:24
Complexity:325

Purity/Quality:

99% ^*data from raw suppliers

Glycidyl Oleate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCC=CCCCCCCCC(=O)OCC1CO1
Isomeric SMILES:CCCCCCCC/C=C\CCCCCCCC(=O)OCC1CO1
Uses Labelled Glycidyl Oleate. Used for preparation of Lysophosphatidic acid analogs as agonists of the edg2 lysophosphatidic acid receptor. Labelled Glycidyl Oleate Glycidyl Oleate is used for preparation of Lysophosphatidic acid analogs as agonists of the edg2 lysophosphatidic acid receptor.

Technology Process of Glycidyl oleate

There total 7 articles about Glycidyl oleate 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: 99.0%