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Monoxerutin

Base Information Edit
  • Chemical Name:Monoxerutin
  • CAS No.:23869-24-1
  • Molecular Formula:C29H34 O17
  • Molecular Weight:654.579
  • Hs Code.:
  • European Community (EC) Number:245-917-9
  • UNII:EKF7043SBU
  • DSSTox Substance ID:DTXSID70905139
  • Nikkaji Number:J34.317J
  • Wikipedia:Monoxerutin
  • Wikidata:Q6902068
  • NCI Thesaurus Code:C77402
  • Metabolomics Workbench ID:144442
  • ChEMBL ID:CHEMBL3527416
  • Mol file:23869-24-1.mol
Monoxerutin

Synonyms:3',4',7-trihydroxyethylrutin;3',4',7-tris(O-(2- hydroxyethyl))rutin;oxerutin;Paroven;Posorutin;Relvene;Rhéoflux;Teboven;Troxérutine Mazal;troxerutin;Troxerutin-ratiopharm;Troxeven;Vastribil;Veinamitol;Veniten retard;Veno SL;Venorutin;venoruton;venoruton P4;Venotrulan Trox;vitamin P4;7-monohydroxyethylrutoside;monoHER

Suppliers and Price of Monoxerutin
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
  • MONOXERUTIN 95.00%
  • 5MG
  • $ 495.24
Total 5 raw suppliers
Chemical Property of Monoxerutin Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:159 - 165°C 
  • Boiling Point:1022.548°C at 760 mmHg 
  • Flash Point:332.089°C 
  • PSA:278.66000 
  • Density:1.759g/cm3 
  • LogP:-2.02160 
  • Storage Temp.:Hygroscopic, -20°C Freezer, Under inert atmosphere 
  • Solubility.:DMSO (Slightly, Sonicated), Methanol (Slightly, Heated, Sonicated) 
  • XLogP3:-1.6
  • Hydrogen Bond Donor Count:10
  • Hydrogen Bond Acceptor Count:17
  • Rotatable Bond Count:9
  • Exact Mass:654.17959961
  • Heavy Atom Count:46
  • Complexity:1070
Purity/Quality:

98%Min *data from raw suppliers

MONOXERUTIN 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OCCO)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O
  • Isomeric SMILES:C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OCCO)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O
  • Uses Monoxerutin is food-derived bioactives can protect anti-inflammatory activity of cortisol with antioxidant-dependent and -independent mechanisms.
Technology Process of Monoxerutin

There total 1 articles about Monoxerutin 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:
rutin; With sodium tetraborate decahydrate; In water; at 40 - 45 ℃;
oxirane; In water; at 40 - 45 ℃; for 6h; Reagent/catalyst;
Guidance literature:
With pyridine; In methanol; at 75 - 80 ℃; Reagent/catalyst; Temperature; Autoclave;
upstream raw materials:

oxirane

rutin

Downstream raw materials:

troxerutin

Refernces Edit
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