ChemicalBook >> CAS DataBase List >>Sotalol hydrochloride

Sotalol hydrochloride

CAS No.
959-24-0
Chemical Name:
Sotalol hydrochloride
Synonyms
DAROB;SOTALEX;SOTACOR;MJ-1999;BETAPACE;DL-MJ 1999;SOTALOL HCL;SOLATOL HCL;Betapace AF;meadjohnson1999
CBNumber:
CB9712098
Molecular Formula:
C12H21ClN2O3S
Molecular Weight:
308.82
MDL Number:
MFCD00242937
MOL File:
959-24-0.mol
Last updated:2024-04-15 15:30:59

Sotalol hydrochloride Properties

Melting point 218-220°C
storage temp. 2-8°C
solubility H2O: 20 mg/mL
form powder
color white to off-white
Water Solubility Soluble in phosphate buffered saline, DMSO, ethanol, water, and methanol.
CAS DataBase Reference 959-24-0(CAS DataBase Reference)
FDA UNII HEC37C70XX

Pharmacokinetic data

Excreted unchanged in urine >90%
Volume of distribution 1.6-2.4(L/kg)
Biological half-life 10-20 / 56

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H303-H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P405-P501a-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
RTECS  PB0826000
HS Code  2935904000
Toxicity LD50 in male mice, rats (mg/kg): 2600, 3450 orally; 670, 680 i.p.; LD50 orally in rabbits: 1000 mg/kg; LD50 i.p. in dogs: 330 mg/kg (Lish)

Sotalol hydrochloride price More Price(39)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHR2798 Sotalol Hydrochloride 959-24-0 500MG $287 2024-03-01 Buy
Sigma-Aldrich 1617408 Sotalol hydrochloride United States Pharmacopeia (USP) Reference Standard 959-24-0 300mg $311.4 2024-03-01 Buy
Sigma-Aldrich 39863 (±)-Sotalol hydrochloride analytical standard 959-24-0 10mg $144 2022-05-15 Buy
Alfa Aesar J63772 Sotalol hydrochloride, 98% 959-24-0 1g $520 2024-03-01 Buy
Alfa Aesar J63772 Sotalol hydrochloride, 98% 959-24-0 5g $858 2024-03-01 Buy
Product number Packaging Price Buy
PHR2798 500MG $287 Buy
1617408 300mg $311.4 Buy
39863 10mg $144 Buy
J63772 1g $520 Buy
J63772 5g $858 Buy

Sotalol hydrochloride Chemical Properties,Uses,Production

Description

Sotalol (hydrochloride) (Item No. 26291) is an analytical reference standard categorized as a β-adrenergic receptor antagonist. It has been detected as an adverse analytical finding (AAF) during anti-doping testing. This product is intended for use in analytical forensic applications. This product is also available as a general research tool .

Description

Sotalol is a non-selective antagonist of β-adrenergic receptors (β-ARs; IC50s = 8.9 and 5.2 μM for β1- and β2-ARs, respectively) and a class III antiarrhythmic agent. It decreases delayed outward potassium currents (IK) in guinea pig ventricular cells and prolongs action potential duration in electrically stimulated isolated guinea pig papillary muscles when used at a concentration of 100 μM. Sotalol decreases heart rate and increases blood pressure and the cardiac functional refractory period (FRP) in a canine model of ventricular tachycardia induced by programmed electrical stimulation (PES). Formulations containing sotalol have been used in the treatment of ventricular arrhythmias and maintenance of normal sinus rhythm in patients with atrial fibrillation or flutter (AFIB/AFL).

Chemical Properties

White Crystalline Solid

Originator

Sotagard,Glaxo

Uses

antibacterial

Uses

Sotalol hydrochloride is used as a potent beta adrenergic antagonist, prolongs the action potential and increases the refractory period. Sotalol hydrochloride is also considered a non-selective β blocker and a potassium channel blocker with an IC50 of 43 μM.

Uses

A potent α-adrenergic receptor antagonist. A class III antiarrythmic. It has been shown to prolong action potential and increases the refractory period.

Uses

A potent -adrenergic receptor antagonist. A class III antiarrythmic. It has been shown to prolong action potential and increases the refractory period

Definition

ChEBI: A hydrochloride salt that is the monohydrochloride of sotalol. It has both beta-adrenoreceptor blocking (Vaughan Williams Class II) and cardiac action potential duration prolongation (Vaughan Williams Class III) antiarrhythmic properties. It is used (usually as the hydrochloride salt) for the management of ventricular and supraventricular arrhythmias.

Manufacturing Process

As a resulting of reaction of methansulfonylchloride reacted with aniline methansulfonanilide was obtained. The methansulfonanilide reacted with bromacetylbromide at the presence of AlCl3 and CS2 and 4-(bromacetyl)- methansulfonanilide was prepeared.
Then to the 4-(bromacetyl)-methansulfonanilide isopropylamine was added to give 4-(1-oxo-2-isopropylaminoethyl)methansulfonanilide.The 4-(1-oxo-2-isopropylaminoethyl)methansulfonanilide was reduced by hydrogenesation in the presence of Pd-C catalyst and sodium borohydride. So 4-(1-hydroxy-2-isopropylaminoethyl)methansulfonanilide was obtained.
The 4-(1-hydroxy-2-isopropylaminoethyl)methansulfonanilide hydrochloride may be prepared by treatment of base with hydrochloric acid.

brand name

Betapace(Berlex); Sorine (Upsher Smith).

Therapeutic Function

Beta-adrenergic blocker, Antiarrhythmic

Biological Activity

A relatively potent pure β adrenergic antagonist, unique in possessing additional class III antiarrhythmic activity. Also available as part of the Mixed Adrenergic Tocriset™ .

Clinical Use

Beta-adrenoceptor blocker:
Treatment of life-threatening ventricular arrhythmias
Prophylaxis of SVT

Veterinary Drugs and Treatments

Sotalol may be useful in the treatment of ventricular tachycardias and, possibly, supraventricular tachycardias in dogs.

Drug interactions

Potentially hazardous interactions with other drugs
Anaesthetics: enhanced hypotensive effect.
Analgesics: NSAIDs antagonise hypotensive effect.
Anti-arrhythmics: increased risk of myocardial depression and bradycardia; increased risk ofbradycardia, myocardial depression and AV block with amiodarone; increased risk of ventricular arrhythmias with amiodarone, dronedarone, disopyramide or procainamide - avoid; increased risk of myocardial depression and bradycardia with flecainide.
Antibacterials: increased risk of ventricular arrhythmias with moxifloxacin - avoid; increased risk of ventricular arrhythmias with delamanid.
Antidepressants: enhanced hypotensive effect with MAOIs; increased risk of ventricular arrhythmias with tricyclics; increased risk of ventricular arrhythmias with citalopram, escitalopram and venlafaxine - avoid.
Antihistamines: increased risk of ventricular arrhythmias with mizolastine - avoid.
Antihypertensives: enhanced hypotensive effect; increased risk of withdrawal hypertension with clonidine; increased risk of first dose hypotensive effect with post-synaptic alpha-blockers such as prazosin.
Antimalarials: increased risk of bradycardia with mefloquine; avoid with artemether and lumefantrine and piperaquine with artenimol - increased risk of ventricular arrhythmias.
Antimuscarinics: increased risk of ventricular arrhythmias with tolterodine.
Antipsychotics: enhanced hypotensive effect with phenothiazines; increased risk of ventricular arrhythmias with amisulpride, droperidol, haloperidol, phenothiazines, pimozide, risperidone, sulpiride or zuclopenthixol - avoid with droperidol and zuclopenthixol.
Antivirals: increased risk of ventricular arrhythmias with saquinavir or telaprevir - avoid.
Atomoxetine: increased risk of ventricular arrhythmias.
Calcium-channel blockers: increased risk of bradycardia and AV block with diltiazem; hypotension and heart failure possible with nifedipine and nisoldipine; asystole, severe hypotension and heart failure with verapamil.
Cytotoxics: possible increased risk of bradycardia with crizotinib; increased risk of ventricular arrhythmias with vandetanib - avoid; increased risk of ventricular arrhythmias with arsenic trioxide, bosutinib, ceritinib, panobinostat and vandetanib.
Diuretics: enhanced hypotensive effect; increased risk of ventricular arrhythmias due to hypokalaemia.
Fingolimod: possibly increased risk of bradycardia.
Ivabradine: increased risk of ventricular arrhythmias.
Moxisylyte: possible severe postural hypotension. Ranolazine: avoid concomitant use.
Sympathomimetics: severe hypertension with adrenaline and noradrenaline and possibly with dobutamine.

Metabolism

Metabolism of sotalol is negligible, and it is excreted unchanged in the urine.

storage

Store at RT

Sotalol hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 245)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652 info@fdachem.com China 8174 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21691 55
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Hebei Jimi Trading Co., Ltd.
+86 319 5273535 bestoneforyou@sina.com CHINA 288 58
Xiamen AmoyChem Co., Ltd
+86-592-6051114 +8618959220845 sales@amoychem.com China 6387 58
Standardpharm Co. Ltd.
86-714-3992388 overseasales1@yongstandards.com United States 14336 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19553 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49390 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-81138252 +86-18789408387 1057@dideu.com China 3487 58

View Lastest Price from Sotalol hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Sotalol hydrochloride pictures 2024-04-15 Sotalol hydrochloride
959-24-0
US $32.00-1.30 / KG 1KG 99% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
Sotalol Hydrochloride pictures 2022-04-05 Sotalol Hydrochloride
959-24-0
US $1.00-100.00 / gram 1gram 99.00%USP 50kg Shaanxi Dideu Medichem Co. Ltd
Sotalol hydrochloride USP/EP/BP pictures 2021-08-12 Sotalol hydrochloride USP/EP/BP
959-24-0
US $1.10 / g 1g 99.9% 100 Tons min Dideu Industries Group Limited

Sotalol hydrochloride Spectrum

4-(2-isopropylamino-1-hydroxyaethyl)methanesulfonailidhydrochlorid 4’-(1-hydroxy-2-(isopropylamino)ethyl)methanesulfonanilidemonohydrochloride 4’-(1-hydroxy-2-(isopropylamino)ethyl)-methanesulfonanilidmonohydrochlorid isopropylaminohydroxyethylmethanesulfonanilidehydrochloride meadjohnson1999 n-isopropyl-beta-(4-methanesulfonamidophenyl)ethanolaminehydrochloride SOTACOR SOTALEX SOTALOL HCL (+/-)-SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE MJ-1999 N-[4-[1-HYDROXY-2-[(1-METHYLETHYL)AMINO]ETHYL]PHENYL]METHANESULFONAMIDE HYDROCHLORIDE N-[4-(1-HYDROXY-2-[ISOPROPYLAMINO]ETHYL)-PHENYL]METHANESULFONAMIDE HYDROCHLORIDE D,L-Sotalol, Hydrochloride MJ-1999, Betapace, Darob, Sotacor, Sotalex 4'-[1-Hydroxy-2-(isopropylamino)ethyl]methanesulfonanilide hydrochloride 4'-[2-(Isopropylamino)-1-hydroxyethyl]methanesulfonanilide monohydrochloride DL-MJ 1999 Methanesulfonamide, N-[4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]phenyl]-, monohydrochloride (9CI) N-Isopropyl-b-(4-methanesulfonamidophenyl)ethanolamine hydrochloride METHANESULPHONANILIDE41HYDROXY2ISOPROPYLAMINOETHYLMONOHYDROCHLORIDE 4'-(1-hydroxy-2-isopropylaminoethyl)methanesulphonanilide hydrochloride BETAPACE DAROB SOLATOL HCL (-N-[4-[1-Hydroxy-2-[(1-Methyl Ethyl) Amino]-ethyl]phenyl]methanesulfonamide SOTALOL HYDROCHLORIDE BP N-4-[1-Hydroxy-2-(isopropylamino)ethyl]methane sulfonanilide hydrochloride Beta-cardone hydrochloride Sotalol Hydrochloride (300 mg) Sotalol hydrochlorid Sotalol (Betapace) Sotalol hydrochloride COS Berlex Laboratories Betapace AF (±)-Sotalol hydrochloride,N-[4-[1-Hydroxy-2-(isopropylamino)ethyl]phenyl]methanesulfonamide hydrochloride MethanesulfonaMide,N-[4-[1-hydroxy-2-[(1-Methylethyl)aMino]ethyl]phenyl]-, hydrochloride (1:1) N-[4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]phenyl]-methanesulfonamide,hydrochloride (1:1) Sotalol hydrochloride CRS N-[4-[(1RS)-1-Hydroxy-2-[(1-methylethyl)amino]ethyl]- phenyl]methanesulfonamide hydrochloride (+)-sotalol hydrochloride Sotalol hydrochloride USP/EP/BP Sotalol HCl (MJ 1999) Sotalol HydrochlorideQ: What is Sotalol Hydrochloride Q: What is the CAS Number of Sotalol Hydrochloride Q: What is the storage condition of Sotalol Hydrochloride Q: What are the applications of Sotalol Hydrochloride Sotalol Hydrochloride (1617408) 959-24-0 C21H21ClN2O3S C12H20N2O3SxHCl C12H20N2O3SClH C12H21ClN2O3S C12H20N2O3SHCl EXCENEL API's Adrenoceptor Amines Aromatics Sulfur & Selenium Compounds