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Dofetilide

Dofetilide

CAS: 115256-11-6

Molecular Formula: C19H27N3O5S2

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Dofetilide - Names and Identifiers

Name Dofetilide
Synonyms Tikosyn
U-68798
Tikosym
Dofetilide
beta-((p-Methanesulfonamidophenethyl)methylamino)methanesulfono-p-phenetidide
Methyl[2-[4-(methylsulfonylamino)phenoxy]ethyl][4-(methylsulfonylamino)phenethyl]amine
N-[4-[2-[2-[4-(methanesulfonamido)phenyl]ethyl-methylamino]ethoxy]phenyl]methanesulfonamide
N-[4-[2-[N-Methyl-2-(4-methylsulfonylaminophenoxy)ethylamino]ethyl]phenyl]methanesulfonamide
N-(4-{2-[Methyl(2-{4-[(methylsulfonyl)amino]phenoxy}ethyl)amino]ethyl}phenyl)methansulfonamid
N-(4-{2-[méthyl(2-{4-[(méthylsulfonyl)amino]phénoxy}éthyl)amino]éthyl}phényl)méthanesulfonamide
N-(4-{2-[Methyl(2-{4-[(methylsulfonyl)amino]phenoxy}ethyl)amino]ethyl}phenyl)methanesulfonamide
N-[4-[2-[Methyl[2-[4-[(methylsulfonyl)amino]phenoxy]ethyl]amino]ethyl]phenyl]methanesulfon Amide
Methanesulfonamide, N-[4-[2-[methyl[2-[4-[(methylsulfonyl)amino]phenoxy]ethyl]amino]ethyl]phenyl]-
Methanesulfonamide, N-(4-(2-(methyl(2-(4-((methylsulfonyl)amino)phenoxy)ethyl)amino)ethyl) phenyl)
CAS 115256-11-6
EINECS 638-817-5
InChI InChI=1/C19H27N3O5S2/c1-22(13-12-16-4-6-17(7-5-16)20-28(2,23)24)14-15-27-19-10-8-18(9-11-19)21-29(3,25)26/h4-11,20-21H,12-15H2,1-3H3
InChIKey IXTMWRCNAAVVAI-UHFFFAOYSA-N

Dofetilide - Physico-chemical Properties

Molecular FormulaC19H27N3O5S2
Molar Mass441.56
Density1.344±0.06 g/cm3(Predicted)
Melting Point147-1490C
Boling Point614.1±65.0 °C(Predicted)
Flash Point325.2°C
Solubility DMSO: >20mg/mL
Vapor Presure5.13E-15mmHg at 25°C
Appearancepowder
Colorwhite to off-white
pKa7.0, 9.0, 9.6(at 25℃)
Storage Condition2-8°C
StabilityStable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
Refractive Index1.613
Physical and Chemical PropertiesCrystallization from ethyl acetate-methanol (10:1), melting point 147~149 °c; Crystallization from hexane-ethyl acetate, melting point 151~152 °c; White crystalline solid has also been reported, melting point 161 °c. pKa 7.0,9.0,9.6. Partition coefficient (Ph = 7.4):0.96.
In vitro studyIn Vitro culture of Xenopus oocytes, Dofetilide blocked HERG currents. In guinea pig myocardium, Dofetilide(1 μm) reduced the amplitude of IKR to 61% of the control current, as measured by a 200 MS test pulse and analysis of the deactivation tail current IKR. In intact canine hearts, Dofetilide increased apico-basal parallax, an increase in ERPs significantly more at the tip than at the basal.
In vivo studyIn old myocardial infarction (MI) dogs, Dofetilide(100 mg/kg, I. P.) did not inhibit arrhythmias induced by two-stage coronary ligation and epinephrine or coronary ligation and reperfusion, but inhibition of reentry arrhythmias caused by PES. In dogs consuming digitalis arrhythmia, Dofetilide also showed antiarrhythmic effects. Dofetilide increases the QT interval and shows such a negative effect of other class III drugs, but differs from other classes in antiarrhythmic profiles with three agents, such as D-sotalol, E-4031, and in its MS-551 does not prevent the occurrence of ventricular fibrillation (VF) immediately after coronary reperfusion, and has certain antiarrhythmic effects on digitalis arrhythmia. In SD rats, Dofetilide causes an increase in resorption, and stage-dependent malformations.

Dofetilide - Risk and Safety

Risk CodesR61 - May cause harm to the unborn child
R48/22 - Harmful danger of serious damage to health by prolonged exposure if swallowed.
R51 - Toxic to aquatic organisms
Safety DescriptionS53 - Avoid exposure - obtain special instructions before use.
S22 - Do not breathe dust.
S36 - Wear suitable protective clothing.
S57 - Use appropriate container to avoid environmental contamination.
WGK Germanynwg
HS Code2935904000

Dofetilide - Nature

Open Data Verified Data

from ethyl acetate methanol (10:1) crystallization, melting point 147~149 deg C; From hexane ethyl acetate crystallization, melting point 151~152 deg C; Also reported as white crystalline solid, melting point 161 °c. pK. 7.0,9.0,9.6. Partition coefficient (pH-7. 4):0.96.

Last Update:2025-06-10 22:55:16

Dofetilide - Preparation Method

Open Data Verified Data

N-methyl -4-nitrophenylethylamine was dissolved in acetonitrile with 2-[4-nitrophenoxy] ethoxy bromide, potassium carbonate and sodium iodide were added, and the reaction was stirred under reflux. It is concentrated to dryness and the remaining oily solid is worked up to give the compound. The obtained compound was dissolved in ethanol and the reaction was catalyzed by Raney nickel. After filtration, the filtrate was concentrated to dryness. The resulting compound and methanesulfonic anhydride were dissolved in dichloromethane and stirred at room temperature. The product was further processed to obtain dofetilide.

Last Update:2022-01-01 09:10:15

Dofetilide - Preparation solution concentration reference

 1mg5mg10mg
1 mM2.265 ml11.323 ml22.647 ml
5 mM0.453 ml2.265 ml4.529 ml
10 mM0.226 ml1.132 ml2.265 ml
5 mM0.045 ml0.226 ml0.453 ml
Last Update:2024-01-02 23:10:35

Dofetilide - Application

Open Data Verified Data

developed by Pfizer Pharmaceuticals Inc. in the United States and marketed in 2000. Dofetilide is a relatively specific Class III antiarrhythmic drug, a selective potassium channel agonist. Treatment and prevention of atrial arrhythmias, such as atrial fibrillation, atrial flutter and paroxysmal supraventricular tachycardia, can also prevent the occurrence of ventricular tachycardia.

Last Update:2025-08-19 16:24:40
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Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
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SKYRUN INDUSTRIAL CO.,LTD
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CAS: 115256-11-6
Tel: +86 0571-86722205
Email: sales@chinaskyrun.com
Mobile: +8618958170122
QQ: 2531159185 Click to send a QQ messageSend QQ message
Wechat: chinaskyrun
Shanghai Yuanye Bio-Technology Co., Ltd.
Product Name: Dofetilide Visit Supplier Webpage Request for quotation
CAS: 115256-11-6
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
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