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Bevantolol

CAS No.
59170-23-9
Chemical Name:
Bevantolol
Synonyms
Bevantolol;NSC 132348;DL-Bevantolol;Bevantolol USP/EP/BP;1-((3,4-DiMethoxyphenethyl)aMino)-3-(M-tolyloxy)propan-2-ol;1-[(3,4-Dimethoxyphenethyl)amino]-3-(m-tolyloxy)-2-propanol;1-(3,4-Dimethoxyphenethylamino)-3-(3-methylphenoxy)-2-propanol;2-Propanol, 1-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-3-(3-methylphenoxy)-
CBNumber:
CB0875462
Molecular Formula:
C20H27NO4
Molecular Weight:
345.43
MDL Number:
MOL File:
59170-23-9.mol
Last updated:2024-10-28 16:48:35

Bevantolol Properties

storage temp. 2-8°C
CAS DataBase Reference 59170-23-9
FDA UNII 34ZXW6ZV21
ATC code C07AB06

Bevantolol price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0009101 BEVANTOLOL 95.00% 59170-23-9 5MG $503.95 2021-12-16 Buy
Crysdot CD31001372 Bevantolol 95+% 59170-23-9 1g $947 2021-12-16 Buy
AvaChem 2822B Bevantolol 59170-23-9 10g $1190 2021-12-16 Buy
AvaChem 2822B Bevantolol 59170-23-9 10mg $39 2021-12-16 Buy
AvaChem 2822B Bevantolol 59170-23-9 100mg $89 2021-12-16 Buy
Product number Packaging Price Buy
API0009101 5MG $503.95 Buy
CD31001372 1g $947 Buy
2822B 10g $1190 Buy
2822B 10mg $39 Buy
2822B 100mg $89 Buy

Bevantolol Chemical Properties,Uses,Production

Originator

Bevantolol hydrochloride,Parke, Davis (Pfizer)

Definition

ChEBI: Bevantolol is a propanolamine that is 3-aminopropane-1,2-diol in which the hydrogen of the primary hydroxy group is substituted by 3-methylphenyl and one of the hydrogens attached to the nitrogen is substituted by 2-(3,4-dimethoxyphenyl)ethyl. A beta1 adrenoceptor antagonist, it has been shown to be as effective as other beta-blockers for the treatment of angina pectoris and hypertension. It has a role as a beta-adrenergic antagonist, a calcium channel blocker, an antihypertensive agent and an anti-arrhythmia drug.

Manufacturing Process

To a solution of 50 g (1.25 mol) of NaOH in 1200 ml H2O was added 108 g (1 mol) of m-cresol freshly distilled and at 15°C in one lot 117ml (1.5 mol) of epichlorohydrin. The emulsion was stirred at room temperature for 16 hours in a creased flask. The product was taken up in 1000 ml of toluene and washed with 500 ml water. Distillation yielded 135.7 g=82% of 3-(m-tolyloxy)-1,2- epoxypropane, b.p. 61°C at 0.05 mm.
Preparation of bevantolol hydrochloride:
To a suitable reactor under a nitrogen blanket is added 13.7 kg of β-(3,4- dimethoxyphenyl)ethylamine. The amine is cooled to 5°C and 12.5 kg of 3- (m-tolyloxy)-1,2-epoxypropane is added maintaining the temperature between 5-10°C. After 10 hours, the mixture is seeded with bevantolol free base; seeding is repeated approximately every 2 hours until it is evident that crystallization has started. After stirring for 48 hours at 10°C, 26 L of hexane is added. The temperature is raised to 25°C and stirring is continued for 48 hours. The slurry is filtered and the collected solid is dried under vacuum. The product is dissolved in 60 L of isopropyl alcohol and the solution is filtered. The reactor and filter are rinsed with 186 L of isopropyl alcohol and 2.7 kg of anhydrous hydrogen chloride is added to the combined filtrate. The batch is heated to reflux for 2 hours. The temperature is adjusted to 65°C and the solution is seeded with bevantolol hydrochloride crystals. The mixture is held at this temperature with stirring until a heavy sand-like slurry is present. The mixture is allowed to cool to ambient temperature without stirring or artificial cooling. It is then cooled to 20°C. The slurry is centrifuged and the product rinsed with isopropyl alcohol until the filtrate is colorless. After being vacuum dried at 50-55°C the product is milled if necessary; yield of bevantolol hydrochloride 22.7 kg (78.6%); melting point 137-138°C.

Therapeutic Function

Antiarrhythmic, Beta-adrenergic blocker

Enzyme inhibitor

This antihypertensive agent (FW = 345.43 g/mol; CAS 59170-23-9), also known by the code name NC-1400 and systematically as (RS)-[2-(3,4- dimethoxyphenyl)ethyl]-[2-hydroxy-3-(3-methylphenoxy)propyl]amine, is a dual-action b-blocker and calcium ion channel blocker. Bevantolol is a selective b1-adrenoceptor blocker with some blocking activity of a1- adrenoceptors.

Bevantolol Preparation Products And Raw materials

Raw materials

Preparation Products

Bevantolol Suppliers

Global( 23)Suppliers
Supplier Tel Email Country ProdList Advantage
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63687 58
ANHUI WITOP BIOTECH CO., LTD
+8615255079626 eric@witopchemical.com China 23541 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 22783 58
Hangzhou MolCore BioPharmatech Co.,Ltd.
+86-057181025280; +8617767106207 sales@molcore.com China 49734 58
TargetMol Chemicals Inc.
+8613564774135 zijue.cai@tsbiochem.com United States 19885 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131957 58
LGM Pharma 1-(800)-881-8210 inquiries@lgmpharma.com United States 2123 70
Aikon International Limited 025-66113011 18112977050 cb6@aikonchem.com China 15494 58
Mianyang Vandino Pharmaceutical Technology Co., Ltd. 0816-1568120-1579 15681201579 1755695756@qq.com China 309 58
TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 24647 58

View Lastest Price from Bevantolol manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Bevantolol pictures 2024-10-28 Bevantolol
59170-23-9
US $1980.00-2500.00 / mg 10g TargetMol Chemicals Inc.
Bevantolol USP/EP/BP pictures 2021-08-13 Bevantolol USP/EP/BP
59170-23-9
US $1.10 / g 1g 99.9% 100 Tons min Dideu Industries Group Limited
  • Bevantolol pictures
  • Bevantolol
    59170-23-9
  • US $1980.00-2500.00 / mg
  • TargetMol Chemicals Inc.
2-Propanol, 1-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-3-(3-methylphenoxy)- DL-Bevantolol NSC 132348 1-(3,4-Dimethoxyphenethylamino)-3-(3-methylphenoxy)-2-propanol 1-[(3,4-Dimethoxyphenethyl)amino]-3-(m-tolyloxy)-2-propanol 1-((3,4-DiMethoxyphenethyl)aMino)-3-(M-tolyloxy)propan-2-ol Bevantolol Bevantolol USP/EP/BP 59170-23-9 C20H27NO4