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ChemicalBook >> CAS DataBase List >>bietaserpine

bietaserpine

CAS No.
53-18-9
Chemical Name:
bietaserpine
Synonyms
S-1210;DL-152;bietaserpine;Bietasperine;Bietaserpinum;Diethylaminoreserpine;(3β,20α)-1-[2-(Diethylamino)ethyl]-11,17α-dimethoxy-18β-[(3,4,5-trimethoxybenzoyl)oxy]yohimban-16β-carboxylic acid methyl;Yohimban-16-carboxylic acid, 1-[2-(diethylamino)ethyl]-11,17-dimethoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]-, methyl ester, (3β,16β,17α,18β,20α)-
CBNumber:
CB7901926
Molecular Formula:
C39H53N3O9
Molecular Weight:
707.86
MDL Number:
MFCD00242906
MOL File:
53-18-9.mol
MSDS File:
SDS
Last updated:2026-04-21 10:31:43
Product description Number Pack Size Price
BIETASERPINE 95.00% API0012898 5MG $501.38

bietaserpine Properties

alpha D17 -121° (c = 2 in CHCl3)
Boiling point 706.92°C (rough estimate)
Density 1.1581 (rough estimate)
refractive index 1.7800 (estimate)
FDA UNII 0P5B94FVD5
ATC code C02AA07,C02AA57

bietaserpine price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0012898 BIETASERPINE 95.00% 53-18-9 5MG $501.38 2021-12-16 Buy
Product number Packaging Price Buy
API0012898 5MG $501.38 Buy

bietaserpine Chemical Properties,Uses,Production

Originator

Tensibar,Lefranco,France,1967

Definition

ChEBI: (1R,15S,17R,18R,19S,20S)-3-[2-(diethylamino)ethyl]-6,18-dimethoxy-17-[oxo-(3,4,5-trimethoxyphenyl)methoxy]-11,12,14,15,16,17,18,19,20,21-decahydro-1H-yohimban-19-carboxylic acid methyl ester is a yohimban alkaloid.

Manufacturing Process

The first stage is to prepare the naphthyl sodium solution in the following way:
To a solution of 0.6 g naphthalene in 10 ml tetrahydrofurane, anhydrous, used as solvent, add 96 mg sodium under a nitrogen atmosphere. After a few minutes, an intensive dark green coloration develops, while the sodium dissolves. The reaction is completed after a period of time ranging between 30 and 60 minutes.
Then add to the above solution a solution of 2.42 g reserpine in 60 ml anhydrous dioxan at 50°C.
After heating for 15 minutes (which corresponds to carrying out reaction a), add 0.6 g, diethylaminochloroethane, while the mixture is kept boiling under reflux, for 6 hours. Reaction b is then completed.
Then cool the mixture and evaporate the dioxan under reduced pressure. The pasty residue is dissolved in a mixture of 50 ml benzene and 20 ml ether, and washed several times with water.
The aqueous solutions resulting from the washing are also extracted with ether, and the ether portions are added to the main ether-benzene solution. This solution is extracted several times with 5% acetic acid, until the silicotungstate test (an identification test for alkaloids) yields a negative result, and the acetic solutions are washed with 10 ml ether.
After combining the acetic extracts, the solution is adjusted to a pH of 9 with sodium carbonate, which precipitates the base, which is insoluble in water. The oily suspension obtained in this way is extracted several times with chloroform. The chloroform solutions are then washed, each with 10 ml water, then they are combined and dried over anhydrous potassium carbonate.
After filtering and evaporating the solvent under reduced pressure, the pasty residue, constituted by the enriched product, is diluted with 30 ml ether and in this way 0.225 g reserpine (which has not taken part in the reaction) is isolated by filtration.
After evaporation of the ether under reduced pressure, 1.525 g of the crude resinous base is obtained, which constitutes the required product in a crude and impure condition.
This product is purified in the following way: After dissolving in 15 ml of dry benzene, the resulting solution is filtered on an alumina column, which fixes the base.
After consecutive elutions with pure benzene, and benzene containing increasing proportions of chloroform,0.748 g of 1-diethylaminoethylreserpineis isolated in the form of a resin. The crystalline acid bitartrate prepared in ethyl acetate melts at 145°-150°C, with decomposition.

Therapeutic Function

Antihypertensive

bietaserpine Preparation Products And Raw materials

Raw materials

Preparation Products

bietaserpine Suppliers

Global( 9)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354; support@targetmol.com United States 39037 58
TargetMol Chemicals Inc.
13564774135 marketing@targetmol.com United States 19956 58
Organtec Ltd 010-89719903 18511074324;18511074324 danlismi@outlook.com China 1334 58
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd 029-029-029-81148696 18161915376 1040@dideu.com China 9999 58
TargetMol Chemicals Inc. 15002134094 marketing@targetmol.cn China 29879 58

View Lastest Price from bietaserpine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Bietaserpine pictures 2026-04-20 Bietaserpine
53-18-9
$1520.00-2500.00 10g TargetMol Chemicals Inc.
(3β,20α)-1-[2-(Diethylamino)ethyl]-11,17α-dimethoxy-18β-[(3,4,5-trimethoxybenzoyl)oxy]yohimban-16β-carboxylic acid methyl Diethylaminoreserpine DL-152 S-1210 bietaserpine Yohimban-16-carboxylic acid, 1-[2-(diethylamino)ethyl]-11,17-dimethoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]-, methyl ester, (3β,16β,17α,18β,20α)- Bietaserpinum Bietasperine 53-18-9 C39H53N3O9
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