ChemicalBook > CAS DataBase List > Sotalol

Sotalol

Product Name
Sotalol
CAS No.
3930-20-9
Chemical Name
Sotalol
Synonyms
SORBITOL;SOTALOL;Sotolol;dl-sotalol;Betacotdone;beta-Cardone;AURORA KA-855;Sotalol USP/EP/BP;Sotalol (base and/or unspecified salts);4’-(1-hydroxy-2-(isopropylamino)ethyl)methanesulfonanilide
CBNumber
CB6277510
Molecular Formula
C12H20N2O3S
Formula Weight
272.36
MOL File
3930-20-9.mol
More
Less

Sotalol Property

Melting point:
206.5-207 °C
Boiling point:
443.3±55.0 °C(Predicted)
Density 
1.298 g/cm3
storage temp. 
Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility 
Chloroform (Slightly, Heated), Methanol (Slightly, Sonicated)
pka
pK1 8.2, pK2 9.8(at 25℃)
form 
Solid
color 
Pale Yellow to Light Yellow
BCS Class
1
Stability:
Hygroscopic
InChI
InChI=1S/C12H20N2O3S/c1-9(2)13-8-12(15)10-4-6-11(7-5-10)14-18(3,16)17/h4-7,9,12-15H,8H2,1-3H3
InChIKey
ZBMZVLHSJCTVON-UHFFFAOYSA-N
SMILES
CS(NC1=CC=C(C(O)CNC(C)C)C=C1)(=O)=O
CAS DataBase Reference
3930-20-9(CAS DataBase Reference)
NIST Chemistry Reference
Methanesulfonanilide, 4'-(1-hydroxy-2-(isopropylamino)ethyl)-(3930-20-9)
EPA Substance Registry System
Methanesulfonamide, N-[4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]phenyl]- (3930-20-9)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H319Causes serious eye irritation

Precautionary statements

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

ApexBio Technology
Product number
B1367
Product name
Sotalol
Packaging
200mg
Price
$119
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0004211
Product name
SOTALOL
Purity
95.00%
Packaging
25MG
Price
$435
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0004211
Product name
SOTALOL
Purity
95.00%
Packaging
100MG
Price
$449
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0004211
Product name
SOTALOL
Purity
95.00%
Packaging
1G
Price
$519
Updated
2021/12/16
Chemenu
Product number
CM276444
Product name
N-(4-(1-Hydroxy-2-(isopropylamino)ethyl)phenyl)methanesulfonamide
Purity
95%
Packaging
1g
Price
$893
Updated
2021/12/16
More
Less

Sotalol Chemical Properties,Usage,Production

Originator

Sotagard,Glaxo

Definition

ChEBI: A sulfonamide that is N-phenylmethanesulfonamide in which the phenyl group is sustituted at position 4 by a 1-hydroxy-2-(isopropylamino)ethyl group. It has both beta-adrenoreceptor blocking (Vaughan Williams Class II) and ardiac 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.

Therapeutic Function

Beta-adrenergic blocker, Antiarrhythmic

World Health Organization (WHO)

Sotalol is a non-selective?-adrenoreceptor antagonist. It should be noted that when stopping sotalol the dose should be reduced gradually.

General Description

Sotalol, 4'[1-hydroxy-2-(isopropylamino)ethyl]methylsulfonanilide (Betapace), is a relatively new antiarrhythmicdrug, characterized most often as a class IIIagent, and although it has effects that are related to the classII agents, it is not therapeutically considered a class II antiarrhythmic.It contains a chiral center and is marketed as theracemic mixture. Because of its enantiomers, its mechanismof action spans two of the antiarrhythmic drug classes. Thel(-) enantiomer has both β-blocking (class II) and potassiumchannel-blocking (class III) activities. The d(+) enantiomerhas class III properties similar to those of the (-) isomer,but its affinity for the -adrenergic receptor is 30 to 60 timeslower.

Biological Activity

sotalol hydrochloride is an adrenergic beta-antagonist that is used in the treatment of life-threatening arrhythmias.

Mechanism of action

Sotalol acts as an antiarrhythmic by β- receptor blockade as well as by prolonging the action potential duration in atrium and ventricle and the refractory period in atrium and AV node . Activity against supraventricular and ventricular arrhythmiaswas demonstrated.

Clinical Use

The sotalol enantiomers produce different effects onthe heart. Class III action of d-sotalol in the sinus node isassociated with slowing of sinus heart rate, whereas -adrenergicblockade contributes to the decrease in heart rate observedwith 1- or d,1-sotalol. Sotalol is not metabolized, noris it bound significantly to proteins. Elimination occurs byrenal excretion, with more than 80% of the drug eliminatedunchanged. Sotalol is characteristic of class III antiarrhythmicdrugs, in that it prolongs the duration of the action potentialand, thus, increases the effective refractory period of myocardialtissue. It is distinguished from the other class III drugs(amiodarone and bretylium) because of its -adrenergicreceptor–blocking action.

Side effects

Side effects of sotalol include those attributed to both β-adrenoceptor blockade and proarrhythmic effects. This arrhythmia is a serious threat, as it may lead to ventricular fibrillation. Adverse effects attributable to its β- blocker activity include fatigue, dyspnea, chest pain, headache, nausea, and vomiting.

Drug interactions

Drugs with inherent QT interval–prolonging activity (i.e., thiazide diuretics and terfenadine) may enhance the class III effects of sotalol.

Precautions

The contraindications that apply to other β-adrenoceptor blocking agents also apply to sotalol. In addition, hypokalemia and drugs known to prolong the QT interval may be contraindicated, as they enhance the possibility of proarrhythmic events.

Sotalol Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Sotalol Suppliers

LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
UHN Shanghai Research & Development Co., Ltd.
Tel
021-58958002 18930822973
Fax
+86 (21) 5895-8628
Email
SALES@UHNSHANGHAI.COM
Country
China
ProdList
977
Advantage
58
Clearsynth Labs Limited
Tel
+91-22-26355700
Fax
+91-22-26355701
Email
info@clearsynth.com
Country
India
ProdList
9679
Advantage
58
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131957
Advantage
58
Changzhou Extraordinary Pharmatech co., LTD.
Tel
+86-519-82111935 15195055733
Fax
051982611250
Email
info@feifanchem.com
Country
China
ProdList
362
Advantage
58
Chengdu Saint - Kay Biotechnology Co., Ltd.
Tel
028-85157043 15882256948
Email
676046971@qq.com
Country
China
ProdList
4390
Advantage
58
Shanghai Han-Xiang Chemical Co., Ltd.
Tel
15971444841
Fax
18327183813
Email
amber@biochempartner.com
Country
China
ProdList
3061
Advantage
58
Xi'an MC Biotech, Co., Ltd.
Tel
029-89275612 +8618991951683
Fax
8618991951683
Email
mcbio_sales@163.com
Country
China
ProdList
2251
Advantage
58
Wuhan Yanzhe Technology Co., Ltd
Tel
15527250409
Fax
QQ:2692360204
Email
wenhaotian12@163.com
Country
China
ProdList
4575
Advantage
58
Foshan Treasure Biotechnology Co., Ltd
Tel
0757-85921206 18520245316
Email
2329783215@qq.com
Country
China
ProdList
12661
Advantage
58
More
Less

View Lastest Price from Sotalol manufacturers

Anhui Zhongda Biotechnology Co., Ltd
Product
Sotalol 3930-20-9
Price
US $0.00-0.00/g
Min. Order
1g
Purity
99%
Supply Ability
100000tons
Release date
2023-08-11
Anhui Zhongda Biotechnology Co., Ltd
Product
Sotalol 3930-20-9
Price
US $90.00-70.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10000/month
Release date
2023-08-07
Anhui Zhongda Biotechnology Co., Ltd
Product
Sotalol 3930-20-9
Price
US $90.00-70.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10000/month
Release date
2023-08-11

3930-20-9, SotalolRelated Search:


  • SOTALOL
  • [(2R)-2-hydroxy-2-[4-(methanesulfonamido)phenyl]ethyl]-propan-2-ylammonium
  • 4'-[1-Hhydroxy-2-(isopropylamino)ethyl]methanesulfonanilide
  • 4'-[1-Hydroxy-2-(isopropylamino)ethyl]metahnesulfonanilide
  • 4'-[1-Hydroxy-2-(isopropylamino)ethyl]methanesulfonanilide
  • 4’-(1-hydroxy-2-(isopropylamino)ethyl)-methanesulfonanilid
  • 4’-(1-hydroxy-2-(isopropylamino)ethyl)methanesulfonanilide
  • beta-Cardone
  • dl-sotalol
  • Methanesulfonamide, N-(4-(1-hydroxy-2-((1-methylethyl)amino)ethyl)phenyl)-
  • Methanesulfonanilide, 4'-(1-hydroxy-2-(isopropylamino)ethyl)-
  • n-(4-(1-hydroxy-2-((1-methylethyl)amino)ethyl)phenyl)-methanesulfonamid
  • N-(4-[1-Hydroxy-2-(isopropylamino)ethyl]phenyl)methanesulfonamide
  • AURORA KA-855
  • DL-4-(2-Isopropylamino-1-hydroxyethyl)methanesulfonanilide
  • Methanesulfonamide, N-[4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]phenyl]- (9CI)
  • Betacotdone
  • Sotalol (base and/or unspecified salts)
  • SORBITOL
  • N-[4-[(R)-1-Hydroxy-2-[(1-methylethyl)amino]ethyl]phenyl]methanesulfonamide
  • (αS)-4-[(Methylsulfonyl)amino]-α-[(isopropylamino)methyl]benzenemethanol
  • N-[4-[(S)-1-Hydroxy-2-[(1-methylethyl)amino]ethyl]phenyl]methanesulfonamide
  • Sotolol
  • Sotalol USP/EP/BP
  • SotalolQ: What is Sotalol Q: What is the CAS Number of Sotalol Q: What is the storage condition of Sotalol Q: What are the applications of Sotalol
  • 3930-20-9
  • C12H20N2O3S