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9,10-Epoxystearic acid

Base Information Edit
  • Chemical Name:9,10-Epoxystearic acid
  • CAS No.:2443-39-2
  • Deprecated CAS:52275-14-6
  • Molecular Formula:C18H34O3
  • Molecular Weight:298.466
  • Hs Code.:2918990090
  • European Community (EC) Number:219-477-3
  • NSC Number:179691
  • DSSTox Substance ID:DTXSID90866879
  • Nikkaji Number:J13.274H
  • Wikidata:Q105116015
  • Metabolomics Workbench ID:77459
  • ChEMBL ID:CHEMBL27918
  • Mol file:2443-39-2.mol
9,10-Epoxystearic acid

Synonyms:9,10-epoxyoctadecanoic acid;9,10-epoxystearic acid;9,10-epoxystearic acid, (cis)-isomer;9,10-epoxystearic acid, (trans)-isomer;9,10-epoxystearic acid, 14C-acid;9,10-epoxystearic acid, ammonium salt;9,10-epoxystearic acid, potassium salt;9,10-epoxystearic acid, sodium salt;cis-9,10-epoxystearic acid

Suppliers and Price of 9,10-Epoxystearic acid
Supply Marketing:Edit
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
  • American Custom Chemicals Corporation
  • TRANS-9,10-EPOXYSTEARIC ACID 95.00%
  • 5MG
  • $ 1163.78
Total 18 raw suppliers
Chemical Property of 9,10-Epoxystearic acid Edit
Chemical Property:
  • Melting Point:53.8 °C 
  • Boiling Point:422.9°Cat760mmHg 
  • PKA:4.78±0.10(Predicted) 
  • Flash Point:141.1°C 
  • PSA:49.83000 
  • Density:0.956g/cm3 
  • LogP:5.31970 
  • Storage Temp.:−20°C 
  • XLogP3:6.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:15
  • Exact Mass:298.25079494
  • Heavy Atom Count:21
  • Complexity:265
Purity/Quality:

99%, *data from raw suppliers

TRANS-9,10-EPOXYSTEARIC ACID 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCC1C(O1)CCCCCCCC(=O)O
Technology Process of 9,10-Epoxystearic acid

There total 22 articles about 9,10-Epoxystearic 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:
Guidance literature:
With tert.-butylhydroperoxide; In decane; at 20 ℃; for 7h; Reagent/catalyst; Time; Catalytic behavior;
DOI:10.1039/c5nj00744e
Guidance literature:
With tert.-butylhydroperoxide; Tween 20; N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid; peroxygenase; In water; at 25 ℃; pH=7.5; Product distribution / selectivity;
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