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Bevantolol

Product Name
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
Formula Weight
345.43
MOL File
59170-23-9.mol
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Bevantolol Property

storage temp. 
2-8°C
CAS DataBase Reference
59170-23-9
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0009101
Product name
BEVANTOLOL
Purity
95.00%
Packaging
5MG
Price
$503.95
Updated
2021/12/16
Crysdot
Product number
CD31001372
Product name
Bevantolol
Purity
95+%
Packaging
1g
Price
$947
Updated
2021/12/16
AvaChem
Product number
2822B
Product name
Bevantolol
Packaging
10g
Price
$1190
Updated
2021/12/16
AvaChem
Product number
2822B
Product name
Bevantolol
Packaging
10mg
Price
$39
Updated
2021/12/16
AvaChem
Product number
2822B
Product name
Bevantolol
Packaging
100mg
Price
$89
Updated
2021/12/16
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Bevantolol Chemical Properties,Usage,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

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Bevantolol Suppliers

LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2127
Advantage
70
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131981
Advantage
58
Aikon International Limited
Tel
025-66113011 18112977050
Fax
(5)02557626880
Email
cb6@aikonchem.com
Country
China
ProdList
15495
Advantage
58
ANHUI WITOP BIOTECH CO., LTD
Tel
+8615255079626
Email
eric@witopchemical.com
Country
China
ProdList
23556
Advantage
58
Dideu Industries Group Limited
Tel
+86-29-89586680 +86-15129568250
Email
1026@dideu.com
Country
China
ProdList
28149
Advantage
58
Mianyang Vandino Pharmaceutical Technology Co., Ltd.
Tel
18990175493 17883072998
Fax
15281123955
Email
1755695756@qq.com
Country
China
ProdList
307
Advantage
58
Shaanxi Dideu Medichem Co. Ltd
Tel
+86-029-81138252 +86-18789408387
Fax
029-88380327
Email
1057@dideu.com
Country
China
ProdList
2756
Advantage
58
TargetMol Chemicals Inc.
Tel
4008200310
Email
marketing@tsbiochem.com
Country
China
ProdList
24018
Advantage
58
Shanghai Haohong Scientific Co., Ltd.
Tel
400-400-8210725
Email
malulu@leyan.com
Country
China
ProdList
40041
Advantage
58
guoyungurui
Tel
18162595016
Email
3287908757@qq.com
Country
China
ProdList
10012
Advantage
58
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View Lastest Price from Bevantolol manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
Bevantolol 59170-23-9
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
20T
Release date
2020-05-11
Dideu Industries Group Limited
Product
Bevantolol 59170-23-9
Price
US $1.10/g
Min. Order
1g
Purity
99.9%
Supply Ability
100 Tons min
Release date
2021-08-12

59170-23-9, BevantololRelated Search:


  • 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