hexobendine dihydrochloride

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Products Intro: Product Name:Hexobendine Dihydrochloride
CAS:50-62-4
Package:250Mg,25Mg
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Products Intro: Product Name:Hexobendine-d18 Dihydrochloride;3,4,5-TriMethoxybenzoic Acid 1,2-Ethanediylbis[(MethyliMino)-3,1-propanediyl] Ester Dihydrochloride; 3,3'-[Ethylenebis(MethyliMino)]di-1-propanol Bis(3,4,5-triMethoxybenzoate) (Ester) Dihydrochloride; AndiaMine; Hexobendin Hydrochloride; Reoxyl
CAS:50-62-4
Purity:98+% Package:1Mg;5Mg;10Mg;50Mg;100Mg;500Mg
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Products Intro: Product Name:Hexobendine Dihydrochloride
CAS:50-62-4
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Products Intro: Product Name:Hexobendine Dihydrochloride
CAS:50-62-4
Purity:NULL Package:250mg;25mg Remarks:NULL
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Products Intro: Product Name:hexobendine dihydrochloride
CAS:50-62-4
Purity:0.99
hexobendine dihydrochloride Basic information
Product Name:hexobendine dihydrochloride
Synonyms:hexobendine dihydrochloride;Andiamine;Ustimon;HEXOBENDINEHYDROCHLORIDE;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
CAS:50-62-4
MF:C30H44N2O10.2ClH
MW:665.603
EINECS:2000547
Product Categories:Amines;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:50-62-4.mol
hexobendine dihydrochloride Structure
hexobendine dihydrochloride Chemical Properties
Melting point 170-174°
storage temp. Hygroscopic, Refrigerator, under inert atmosphere
solubility Methanol (Slightly), Water (Slightly)
form Solid
color White to Pale Beige
Safety Information
MSDS Information
hexobendine dihydrochloride Usage And Synthesis
OriginatorReoxyl,Hormonchemie,W. Germany,1966
UsesHexobendine is used as vasodilator (coronary).
UsesHexobendine dihydrochloride is used as vasodilator (coronary).
Manufacturing ProcessMethylacrylate 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 FunctionVasodilator
hexobendine dihydrochloride Preparation Products And Raw materials
Raw materials3,4,5-Trimethoxybenzoyl chloride-->N,N'-Dimethyl-1,2-ethanediamine-->Methyl acrylate-->Lithium Aluminum Hydride
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