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Moxaverine hydrochloride

CAS No.
1163-37-7
Chemical Name:
Moxaverine hydrochloride
Synonyms
Ben;Eupaverin;Meteverine;MoxaverineHCl;Eupaverin hydrochloride;MOXAVERINE HYDROCHLORIDE;1-benzyl-3-ethyl-6,7-dimethoxyisoquinolinium chloride
CBNumber:
CB3203101
Molecular Formula:
C20H22ClNO2
Molecular Weight:
343.85
MDL Number:
MFCD00800728
MOL File:
1163-37-7.mol
Last updated:2024-09-03 12:56:46
Product description Number Pack Size Price
MOXAVERINE HYDROCHLORIDE 95.00% API0024976 5MG $505.04

Moxaverine hydrochloride Properties

Melting point 208-210° (dec)
FDA UNII 6R0I0E99CN

Moxaverine hydrochloride price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0024976 MOXAVERINE HYDROCHLORIDE 95.00% 1163-37-7 5MG $505.04 2021-12-16 Buy
Product number Packaging Price Buy
API0024976 5MG $505.04 Buy

Moxaverine hydrochloride Chemical Properties,Uses,Production

Originator

Paverin,Bracco

Uses

Moxaverine Hydrochloride is used as a nanocomposites as drug-carriers.

Manufacturing Process

166 g (1 mol) of 3,4-dimethoxybenzaldehyde were stirred for several hours (8 to 10 hours) with 180 g (2.02 mols.) of 1-nitropropane in 300 ml of methanol, in which 12 g of metallic sodium had previously been dissolved, the stirring taking place while heating to 45-50°C. After usual working up of the reaction mixture, there were obtained 155 g of a white, crystalline product, which constituted the 1-(3,4-dimethoxyphenyl)-2-nitro-1-butanol and melted after recrystallization from isopropanol at 93-94°C (uncorrected). The composition was confirmed by elementary analysis and an infra-red spectrogram.
204 g (0.8 mol) of the above nitro alcohol were reduced at 30-35°C in 1250 g of 44% formic acid with 320 g of powdered zinc (about 4.9 at.). After working up, the base 1-(3,4-dimethoxyphenyl)-2-amino-1-butanol was obtained as a white crystalline product. After recrystallization from ethyl acetate, it melted at 91-93°C and the yield was 168 g, i.e. 93.3% of the theoretical.
90 g (0.4 mol) of the above amino alcohol are reacted at 45-50°C in 400 ml of chloroform in the presence of 95 g (1.2 mols) of pyridine by means of 139 g (0.9 mol) of phenylacetic acid chloride. After working up the reaction mixture, a yellowish-crystalline product was isolated (183.5 g, theoretical: 184.6 g), which melted at 123-125°C. After recrystallization from ethyl acetate, it yielded minute, white crystals, which melted at 129 -131°C (uncorrected). The composition of the product was confirmed by elementary analysis.
217 g of the above 1-(3,4-dimethoxyphenyl)-2-(phenylacetamido)-butanol-1- phenyl acetate (0.47 mol) were stirred in 80 1300 ml of xylene with 145 g of phosphorous oxychloride at 100-105°C. After some hours, when the evolution of hydrochloric acid gas had ceased, the reaction mixture was poured on to ice and stirred while cold until the crystallization was completed. After filtering, 144 g (89%) of the formed 1-benzyl-6,7-dimethoxy-3-ethyl isoquinoline hydrochloride were obtained in the form of yellowish crystals, which melted at 198-202°C with decomposition. From the separated aqueous mother liquors, the remainder of the formed isoquinoline base was obtained after treatment with ammonia and extraction with ether, the said base being isolated by way of the sparingly soluble and readily crystallisable acid sulfate. The salt represented a yellowish crystal powder, which melted at 239-243°C and weighed 21 g (11%). Thus, the yield of crude isoquinoline salt was almost the theoretical yield. The crude hydrochloride acid salt yielded white, lustrous prisms after recrystallisation from 96% ethanol, the said prisms melting at 208-210°C with decomposition. 1-Benzyl-6,7 -dimethoxy-3-ethyl isoquinoline may be prepared as a base from its salt by adding of equivalent of triethyl amine or any other base.

Therapeutic Function

Spasmolytic

Moxaverine hydrochloride Preparation Products And Raw materials

Moxaverine hydrochloride Suppliers

Global( 21)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Dideu Medichem Co. Ltd
+86-29-81148696 +86-17392712697 1022@dideu.com China 3996 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49975 58
Career Henan Chemica Co
+86-0371-86658258 +8613203830695 laboratory@coreychem.com China 30229 58
DAYANG CHEM (HANGZHOU) CO.,LTD
+86-88938639 +86-17705817739 info@dycnchem.com China 53899 58
Hubei Yangxin Medical Technology Co., Ltd. 15374522761 3003392093@qq.com China 10000 55
Block Chemical Technology (Shanghai) Co., LTD 021-20432219 13918097649 li_jinfei@acblock-lab.com China 9669 58
Shanghai Yaji Biological Technology Co., Ltd. 021-34661275 15301693058 yajikit@163.com China 9896 58
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd 029-029-81120477 17792793610 1033@dideu.com China 9898 58
TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 24989 58
DSMZ-German Collection of Microorganisms and Cell Cultures GmbH 49053126160 contact@dsmz.de China 6824 58

View Lastest Price from Moxaverine hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Moxaverine hydrochloride pictures 2024-09-03 Moxaverine hydrochloride
1163-37-7
US $0.00-0.00 / KG 1KG 99.0% 10 tons Shaanxi Dideu Medichem Co. Ltd
MOXAVERINE HYDROCHLORIDE 1-benzyl-3-ethyl-6,7-dimethoxyisoquinolinium chloride MoxaverineHCl Eupaverin Meteverine Ben Eupaverin hydrochloride 1163-37-7 C20H21NO2HCl