THREO-9,10-DIHYDROXYSTEARIC ACID

Base Information

Chemical Name:THREO-9,10-DIHYDROXYSTEARIC ACID
CAS No.:2391-05-1
Molecular Formula:C₁₈H₃₆O₄
Molecular Weight:316.481
Hs Code.:
UNII:SQL1V605V5
Metabolomics Workbench ID:70938
Nikkaji Number:J612.388K
Wikidata:Q27289346
Mol file:2391-05-1.mol

Synonyms:Octadecanoicacid, 9,10-dihydroxy-, (R*,R*)-; Octadecanoic acid, 9,10-dihydroxy-, threo-(8CI); threo-9,10-Dihydroxyoctadecanoic acid; threo-9,10-Dihydroxystearic acid;trans-9,10-Dihydroxystearic acid

Suppliers and Price of THREO-9,10-DIHYDROXYSTEARIC ACID

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

Medical Isotopes, Inc.
racthreo-9,10-DihydroxystearicAcid
0.5 g
$ 1960.00

TRC
racthreo-9,10-DihydroxystearicAcid
1g
$ 1070.00

Total 5 raw suppliers

Chemical Property of THREO-9,10-DIHYDROXYSTEARIC ACID

Chemical Property:

Melting Point:92-94?C
PSA：77.76000
LogP:4.27410
Storage Temp.:−20°C
XLogP3:5.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:16
Exact Mass:316.26135963
Heavy Atom Count:22
Complexity:256

Purity/Quality:

99% ^*data from raw suppliers

racthreo-9,10-DihydroxystearicAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCC(C(CCCCCCCC(=O)O)O)O
Isomeric SMILES:CCCCCCCC[C@H]([C@@H](CCCCCCCC(=O)O)O)O
Uses A compound having PPAR ligand activity containing hydroxy fatty acids. A metabolite of oleic acid. A compound having PPAR ligand activity containing hydroxy fatty acids.

Technology Process of THREO-9,10-DIHYDROXYSTEARIC ACID

There total 113 articles about THREO-9,10-DIHYDROXYSTEARIC ACID 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: 92.0%