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Mexiletine

Base Information Edit
  • Chemical Name:Mexiletine
  • CAS No.:31828-71-4
  • Molecular Formula:C11H17NO
  • Molecular Weight:179.262
  • Hs Code.:2922299090
  • European Community (EC) Number:250-825-7
  • UNII:1U511HHV4Z
  • DSSTox Substance ID:DTXSID8048446
  • Nikkaji Number:J19.958C
  • Wikipedia:Mexiletine
  • Wikidata:Q420377
  • NCI Thesaurus Code:C62047
  • RXCUI:6926
  • Pharos Ligand ID:NGCHGGMTAKG5
  • Metabolomics Workbench ID:42747
  • ChEMBL ID:CHEMBL558
  • Mol file:31828-71-4.mol
Mexiletine

Synonyms:KO 1173;KO-1173;KO1173;KOE 1173;KOE-1173;KOE1173;Mexiletene;Mexiletine;Mexiletine Hydrochloride;Mexitil;Mexitil PL;Mexityl;Novo Mexiletine;Novo-Mexiletine

Suppliers and Price of Mexiletine
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
  • TRC
  • 1-(2,6-Dimethylphenoxy)-2-aminopropane
  • 1g
  • $ 45.00
  • Matrix Scientific
  • 1-(2,6-Dimethylphenoxy)-2-aminopropane 97%
  • 1g
  • $ 94.00
  • Matrix Scientific
  • 1-(2,6-Dimethylphenoxy)-2-aminopropane 97%
  • 10g
  • $ 383.00
  • Crysdot
  • 1-(2,6-Dimethylphenoxy)propan-2-amine 97%
  • 10g
  • $ 360.00
  • Atlantic Research Chemicals
  • 1-(2,6-Dimethylphenoxy)-2-aminopropane 95%
  • 10gm:
  • $ 159.06
  • American Custom Chemicals Corporation
  • MEXILETINE 95.00%
  • 2.5G
  • $ 456.00
  • American Custom Chemicals Corporation
  • MEXILETINE 95.00%
  • 1G
  • $ 427.00
  • Alichem
  • 1-(2,6-Dimethylphenoxy)propan-2-amine
  • 10g
  • $ 396.76
  • AK Scientific
  • Mexiletine
  • 100g
  • $ 486.00
Total 33 raw suppliers
Chemical Property of Mexiletine Edit
Chemical Property:
  • Vapor Pressure:0.00642mmHg at 25°C 
  • Melting Point:203-205 °C 
  • Boiling Point:271.5 °C at 760 mmHg 
  • PKA:pKa 9.14± 0.01(H2O,t =25±0.2,I=0.01(NaCl))(Approximate) 
  • Flash Point:112.2 °C 
  • PSA:35.25000 
  • Density:0.979 g/cm3 
  • LogP:2.72970 
  • Storage Temp.:2-8°C 
  • Solubility.:ethanol: 50 mg/mL 
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:179.131014166
  • Heavy Atom Count:13
  • Complexity:139
Purity/Quality:

99.9% *data from raw suppliers

1-(2,6-Dimethylphenoxy)-2-aminopropane *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn 
  • Hazard Codes:Xn 
  • Statements: 20/21/22 
  • Safety Statements: 36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Drug Classes:Antiarrhythmic Agents
  • Canonical SMILES:CC1=C(C(=CC=C1)C)OCC(C)N
  • Recent ClinicalTrials:The Effect of Late Na Current Blocker Mexiletine on Giant T-wave Electrical Alternans(STOP-TWA)
  • Recent EU Clinical Trials:Treatment of Myotonia - Lamotrigine versus Namuscla
  • Recent NIPH Clinical Trials:The clinical trial to assess efficacy of mexiletine for amyotrophic lateral sclerosis
  • Uses Cardiac depressant (anti-arrhythmic). Mexiletine is used for ventricular extrasystole and ventricular tachycardia, and ventricular fibrillation (including during the severe period of myocardial infarction). Mexiletine is a useful analgesia.It is used in treatment of amyotrophic lateral sclerosis comprising administering a bile acid and a phenylbutyrate compound and an additional therapeutic agent.
  • Therapeutic Function Antiarrhythmic
  • Clinical Use Mexiletine (Mexitil) is an antiarrhythmic agent with pharmacological and antiarrhythmic properties similar to those of lidocaine and tocainide. Like tocainide,mexiletine is available for oral administration. Mexiletine is useful as an antiarrhythmic agent in the management of patients with either acute or chronic ventricular arrhythmias.While it is not at present an indication for use, there is interest in using mexiletine to treat the congenital long QT syndrome when an abnormality in the SCN5A gene (LQTS 3) has been found.
  • Drug interactions An upward adjustment in dose may be required when mexiletine is administered with phenytoin or rifampin, since these drugs stimulate the hepatic metabolism of mexiletine, reducing its plasma concentration.
Technology Process of Mexiletine

There total 31 articles about Mexiletine 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:
RS-mexiletine; With L-amino acid oxidase from Crotalus adamanteus; ω-transaminase from Chromobacterium violaceum DSM 30191; sodium pyruvate; at 30 ℃; for 24h; pH=7; Resolution of racemate; aq. phosphate buffer;
With glucose dehydrogenase; D-Alanine; D-glucose; ω-Transaminases ATA-117; C21H28N7O14P2(1+); at 30 - 75 ℃; optical yield given as %ee; aq. phosphate buffer; Enzymatic reaction;
DOI:10.1021/ol901834x
Guidance literature:
With 4-methoxy-N-(1-(naphthalen-2-yl)ethylidene)aniline; ammonium formate; In methanol; at 80 ℃; for 6h; chemoselective reaction; Inert atmosphere;
DOI:10.1002/chem.201303541

Reference yield: 91.0%

Guidance literature:
With ammonium formate; In methanol; at 80 ℃; for 0.166667h; Inert atmosphere;
With formic acid; C29H32ClIrNO; triethylamine; In methanol; at 80 ℃;
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