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Eupatilin

Base Information Edit
  • Chemical Name:Eupatilin
  • CAS No.:22368-21-4
  • Molecular Formula:C18H16O7
  • Molecular Weight:344.321
  • Hs Code.:2932999099
  • UNII:4D58O05490
  • ChEMBL ID:CHEMBL312750
  • DSSTox Substance ID:DTXSID30176904
  • Metabolomics Workbench ID:24311
  • Nikkaji Number:J16.781I
  • NSC Number:122413
  • Wikidata:Q3060385
  • Wikipedia:Eupatilin
  • Mol file:22368-21-4.mol
Eupatilin

Synonyms:5,7-dihydroxy-3',4',6-trimethoxyflavone;eupatilin

Suppliers and Price of Eupatilin
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
  • Usbiological
  • Eupatilin
  • 5mg
  • $ 333.00
  • Usbiological
  • Eupatilin
  • 20mg
  • $ 349.00
  • TRC
  • Eupatilin
  • 5mg
  • $ 65.00
  • Medical Isotopes, Inc.
  • Eupatilin
  • 5 mg
  • $ 650.00
  • Medical Isotopes, Inc.
  • Eupatilin
  • 50 mg
  • $ 2200.00
  • JR MediChem
  • Eupatilin(NewProduct) 98%
  • 100mg
  • $ 268.00
  • JR MediChem
  • Eupatilin(NewProduct) 98%
  • 1g
  • $ 1280.00
  • DC Chemicals
  • Eupatilin >99%
  • 1 g
  • $ 1200.00
  • DC Chemicals
  • Eupatilin >99%
  • 250 mg
  • $ 600.00
  • Crysdot
  • Eupatilin 98+%
  • 25mg
  • $ 190.00
Total 97 raw suppliers
Chemical Property of Eupatilin Edit
Chemical Property:
  • Vapor Pressure:3.21E-14mmHg at 25°C 
  • Melting Point:236-238 °C 
  • Refractive Index:1.627 
  • Boiling Point:583.6 °C at 760mmHg 
  • PKA:6.47±0.40(Predicted) 
  • Flash Point:214.7 °C 
  • PSA:98.36000 
  • Density:1.387 g/cm3 
  • LogP:2.89700 
  • Storage Temp.:Keep in dark place,Sealed in dry,Store in freezer, under -20°C 
  • Solubility.:Acetonitrile (Slightly), DMSO (Slightly), Methanol (Slightly, Heated) 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:4
  • Exact Mass:344.08960285
  • Heavy Atom Count:25
  • Complexity:520
Purity/Quality:

≥98% *data from raw suppliers

Eupatilin *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC
  • Recent ClinicalTrials:Compare the Effect of Eupatilin and Rebamipide on the Prevention of Gastroenteropathy
  • Uses Eupatilin maintains anticoagulant and antiplatelet activity isolated from the Artemisia princeps Pampanini flower.
Technology Process of Eupatilin

There total 16 articles about Eupatilin 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: 85.6%

Guidance literature:
With scandium tris(trifluoromethanesulfonate); In 1,2-dichloro-ethane; for 24h; Reagent/catalyst; Reflux; Sealed tube;
Guidance literature:
With hydrogenchloride; aluminium trichloride; In chloroform; acetonitrile;
Guidance literature:
Multi-step reaction with 9 steps
1: potassium carbonate / acetone / 60 °C
3: potassium hydroxide; pyridine / diethylene glycol; water / 100 °C
4: pyridine; dipotassium peroxodisulfate; tetraethylammonium hydroxide / water / 24 h / 20 °C
5: acetone / 5 h / Reflux
6: potassium hydroxide / ethanol / 20 °C
7: selenium(IV) oxide / i-Amyl alcohol / Reflux
8: hydrogen; palladium 10% on activated carbon / chloroform / 20 °C
9: aluminum (III) chloride / acetonitrile / 1.5 h / Reflux
With pyridine; selenium(IV) oxide; aluminum (III) chloride; dipotassium peroxodisulfate; palladium 10% on activated carbon; hydrogen; tetraethylammonium hydroxide; potassium carbonate; potassium hydroxide; In ethanol; i-Amyl alcohol; chloroform; water; acetone; acetonitrile; diethylene glycol;
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