Vernolic acid

Base Information

Chemical Name:Vernolic acid
CAS No.:17966-13-1
Molecular Formula:C18H32 O3
Molecular Weight:296.45
Hs Code.:
UNII:4S5JF40ZOQ,FR42854EPW
DSSTox Substance ID:DTXSID40895851
Nikkaji Number:J9.572I
Wikipedia:Vernolic_acid
Wikidata:Q28530676
Metabolomics Workbench ID:2318,201063
Mol file:17966-13-1.mol

Synonyms:cis-12-epoxyoctadeca-cis-9-enoate;cis-12-epoxyoctadeca-cis-9-enoic acid;vernoleate;vernolic acid

Suppliers and Price of Vernolic 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

Total 5 raw suppliers

Chemical Property of Vernolic acid

Chemical Property:

Vapor Pressure:2.29E-07mmHg at 25°C
Boiling Point:395.8°Cat760mmHg
Flash Point:130°C
PSA：49.83000
Density:0.969g/cm³
LogP:5.09570
XLogP3:5.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:14
Exact Mass:296.23514488
Heavy Atom Count:21
Complexity:299

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCC1C(O1)CC=CCCCCCCCC(=O)O
Isomeric SMILES:CCCCC[C@@H]1[C@@H](O1)C/C=C\CCCCCCCC(=O)O
Uses (±)-cis-12,13-Epoxy-9(Z)-octadecenoic Acid, an isomer of (-)-Vernolic Acid (V128710). a fatty acid that is monounsaturated and contains an epoxide. It is It is the cis epoxide derived from the C12–C13 alkene of linoleic acid, and an isomer of coronaric acid. Vernolic acid is the key component in vernonia oil, which is produced in abundance by the genera Vernonia and Euphorbia and is a potentially useful biofeedstock.

Technology Process of Vernolic acid

There total 5 articles about Vernolic 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:

: 60-33-3,116745-32-5,26085-09-6,64080-88-2,7049-66-3,949900-18-9,60476-23-5,6144-28-1,67922-65-0,89718-18-3
linoleic acid

: 16833-56-0,61949-82-4,65167-83-1,110658-06-5,113972-57-9,126639-25-6,132201-82-2,135094-09-6,146987-78-2
(+/-)-cis-9,10-epoxy-12(Z)-octadecenoic acid

: 17966-13-1,16833-57-1,7576-35-4
(+/-)-cis-12,13-epoxy-9(Z)-octadecenoic acid

Guidance literature:: With peroxygenase from tomato yeast extract; dihydrogen peroxide; In aq. acetate buffer; at 30 ℃; for 1h; pH=6; Enzymatic reaction;
DOI:10.1016/j.phytochem.2013.02.020