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Verapamil

Base Information Edit
  • Chemical Name:Verapamil
  • CAS No.:52-53-9
  • Deprecated CAS:56949-77-0,7482-85-1,1007128-78-0
  • Molecular Formula:C27H38N2O4
  • Molecular Weight:454.61
  • Hs Code.:
  • European Community (EC) Number:200-145-1
  • UNII:CJ0O37KU29
  • DSSTox Substance ID:DTXSID9041152
  • Nikkaji Number:J4.132G,J332.327G
  • Wikipedia:Verapamil
  • Wikidata:Q410291
  • NCI Thesaurus Code:C928
  • RXCUI:11170
  • Pharos Ligand ID:C4B57RM89FV7
  • Metabolomics Workbench ID:37889
  • ChEMBL ID:CHEMBL6966
  • Mol file:52-53-9.mol
Verapamil

Synonyms:Calan;Cordilox;Dexverapamil;Falicard;Finoptin;Hydrochloride, Verapamil;Iproveratril;Isoptin;Isoptine;Izoptin;Lekoptin;Verapamil;Verapamil Hydrochloride

Suppliers and Price of Verapamil
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
  • ChemScene
  • Verapamil 98.82%
  • 50mg
  • $ 85.00
  • American Custom Chemicals Corporation
  • VERAPAMIL 95.00%
  • 100G
  • $ 43100.00
  • AK Scientific
  • Verapamil
  • 5g
  • $ 851.00
  • AHH
  • Verapamil 98%
  • 1g
  • $ 310.00
  • Activate Scientific
  • Verapamil 98%
  • 250 mg
  • $ 191.00
Total 65 raw suppliers
Chemical Property of Verapamil Edit
Chemical Property:
  • Appearance/Colour:Viscous, pale yellow oil. 
  • Melting Point:25°C 
  • Refractive Index:1.5448 
  • Boiling Point:586.1 °C at 760 mmHg 
  • PKA:8.6(at 25℃) 
  • Flash Point:308.3 °C 
  • PSA:63.95000 
  • Density:1.058 g/cm3 
  • LogP:5.09308 
  • Storage Temp.:Keep in dark place,Inert atmosphere,Room temperature 
  • XLogP3:3.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:13
  • Exact Mass:454.28315770
  • Heavy Atom Count:33
  • Complexity:606
Purity/Quality:

99% *data from raw suppliers

Verapamil 98.82% *data from reagent suppliers

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

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Drug Classes:Cardiovascular Agents
  • Canonical SMILES:CC(C)C(CCCN(C)CCC1=CC(=C(C=C1)OC)OC)(C#N)C2=CC(=C(C=C2)OC)OC
  • Recent ClinicalTrials:The Intra-arterial Vasospasm Trial
  • Recent EU Clinical Trials:Quinidine versus verapamil in short-coupled idiopathic ventricular fibrillation: An open label, randomized crossover pilot trial
  • Recent NIPH Clinical Trials:Comparison of plasma concentrations of verapamil in healthy adults using simple suspension
  • Uses Vasodilator (coronary). Verapamil is primarily used as an antiarrythmic for treating ventricular arrhythmias; however, currently it is being forced out gradually by adenosine. Verapamil is used for preventing angina pectoris attacks, arterial hypertension, and treating and preventing supraventricular arrhythmia (paroxysmal supraventricular tachycardia, atrial fibrillation, atrial flutter, extrasystole).
  • Clinical Use Verapamil (Isoptin, Covera), in addition to its use as an antiarrhythmic agent, has been employed extensively in the management of variant (Prinzmetal’s) angina and effort-induced angina pectoris. It selectively inhibits the voltage-gated calcium channel that is vital for action potential genesis in slowresponse myocytes, such as those found in the sinoatrial and A-V nodes. Verapamil is useful for slowing the ventricular response to atrial tachyarrhythmias, such as atrial flutter and fibrillation. Verapamil is also effective in arrhythmias supported by enhanced automaticity, such as ectopic atrial tachycardia and idiopathic left ventricular tachycardia.
Technology Process of Verapamil

There total 7 articles about Verapamil 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 formic acid; palladium on activated charcoal; In ethanol; at 100 ℃; for 18h;
DOI:10.1021/ja053027x
Guidance literature:
With hydrogen; palladium-carbon; In ethyl acetate; isopropyl alcohol;
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