• ChemicalBook
    Chinese Japanese Germany Korea

    hexobendine dihydrochloride

    hexobendine dihydrochloride
    hexobendine dihydrochloride structure
    CAS No.
    Chemical Name:
    hexobendine dihydrochloride
    Reoxyl;Ustimon;Andiamine;Hexobendin Hydrochloride;HEXOBENDINEHYDROCHLORIDE;hexobendine dihydrochloride;Hexobendine-d18 Dihydrochloride;3,3'-[Ethylenebis(MethyliMino)]di-1-propanol Bis(3,4,5-triMethoxybenzoate) (Ester) Dihydrochloride;3,4,5-TriMethoxybenzoic Acid 1,2-Ethanediylbis[(MethyliMino)-3,1-propanediyl] Ester Dihydrochloride;3-[methyl-[2-[methyl-[3-(3,4,5-trimethoxybenzoyl)oxypropyl]amino]ethyl]amino]propyl 3,4,5-trimethoxybenzoate dihydrochloride
    Molecular Formula:
    Formula Weight:
    MOL File:

    hexobendine dihydrochloride Properties

    Melting point:

    hexobendine dihydrochloride Chemical Properties,Uses,Production


    Reoxyl,Hormonchemie,W. Germany,1966


    Hexobendine dihydrochloride is used as vasodilator (coronary).

    Manufacturing Process

    Methylacrylate and N,N'-dimethylethylenediamine are first reacted and that product reduced with lithium aluminum hydride to give a compound A.
    To a solution of 13 parts of compound A and 12 parts by volume of absolute pyridine in 80 parts by volume of absolute dioxane there are added dropwise and under constant stirring 35 parts of 3,4,5-trimethoxybenzoyl chloride dissolved in 70 parts by volume of absolute dioxane in the course of 30 minutes. The mixture is stirred for a further 3 hours at a temperature of 100°C and the excess solvent is then evaporated in vacuo. The residue of the evaporation is treated with ethyl acetate and saturated sodium carbonate solution, whereafter the organic phase is separated, treated with water, dried with sodium sulfate and the solvent is removed in vacuo. The residue thus obtained is taken up in ether and separated from 4 parts of insoluble trimethoxybenzoic acid anhydride by filtration. After evaporation of the ether there are obtained 32.5 parts of N,N'-dimethyl-N,N'-bis-[3-(3,4,5- trimethoxybenzoxy)propyl]-ethylene diamine, corresponding to a yield of 86% of the theoretical. MP: 75°C to 77°C.
    The di-tertiary base thus obtained is dissolved in ether and the solution is saturated with hydrogen chloride gas. After isolation and reprecipitation from methanol-ether there is obtained the dihydrochloride melting at 170°C to 174°C.

    Therapeutic Function


    hexobendine dihydrochloride Preparation Products And Raw materials

    Raw materials

    Preparation Products

    hexobendine dihydrochloride Suppliers

    Global( 7)Suppliers
    Supplier Tel Fax Email Country ProdList Advantage
    J & K SCIENTIFIC LTD. 400-666-7788 010-82848833-
    86-10-82849933 jkinfo@jkchemical.com;market6@jkchemical.com China 96815 76
    Chemsky (shanghai) International Co.,Ltd 021-50135380
    shchemsky@sina.com China 15424 60
    Shenzhen Polymeri Biochemical Technology Co., Ltd. 400-002-6226
    sales@biochemall.cn China 54467 58
    Energy Chemical 400-005-6266 021-58432009-
    021-58436166 marketing@energy-chemical.com China 44747 58

    • hexobendine dihydrochloride
    • Andiamine
    • Ustimon
    • Reoxyl
    • 3,4,5-trimethoxybenzoic acid 3-[methyl-[2-[methyl-[3-(3,4,5-trimethoxybenzoyl)oxypropyl]amino]ethyl]amino]propyl ester dihydrochloride
    • 3-[methyl-[2-[methyl-[3-(3,4,5-trimethoxybenzoyl)oxypropyl]amino]ethyl]amino]propyl 3,4,5-trimethoxybenzoate dihydrochloride
    • 3-[methyl-[2-[methyl-[3-(3,4,5-trimethoxyphenyl)carbonyloxypropyl]amino]ethyl]amino]propyl 3,4,5-trimethoxybenzoate dihydrochloride
    • 3,3'-[Ethylenebis(MethyliMino)]di-1-propanol Bis(3,4,5-triMethoxybenzoate) (Ester) Dihydrochloride
    • 3,4,5-TriMethoxybenzoic Acid 1,2-Ethanediylbis[(MethyliMino)-3,1-propanediyl] Ester Dihydrochloride
    • Hexobendin Hydrochloride
    • Hexobendine-d18 Dihydrochloride
    • 50-62-4
    • Amines
    • Aromatics
    • Intermediates & Fine Chemicals
    • Pharmaceuticals
    Copyright 2017 ? ChemicalBook. All rights reserved