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Mesoridazine Besylate

CAS No.
32672-69-8
Chemical Name:
Mesoridazine Besylate
Synonyms
nc123;SERENTIL;MESORIDAZINE BESYLATE;MESORIDAZINE BENZENESULFONATE;Mesoridazine Besylate (250 mg);Mesoridazine Besylate (1393005);Mesoridazine Besilate (10-[2-[(2RS);ylsulfinyl)ethyl)-10h-phenothiazine(1:1);Mesoridazine benzenesulfonate|||Serentil;Thioridazine Hydrochloride Impurity B as Besilate
CBNumber:
CB2295822
Molecular Formula:
C27H32N2O4S3
Molecular Weight:
544.75
MDL Number:
MFCD00800983
MOL File:
32672-69-8.mol
Last updated:2024-11-20 11:41:24

Mesoridazine Besylate Properties

Melting point 174-175 °C
storage temp. 2-8°C
solubility DMSO: 10 mg/mL
form solid
color white
Stability Hygroscopic
FDA UNII T4G2I958J2

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P301+P312+P330
Hazard Codes  Xn
Risk Statements  22
WGK Germany  3
RTECS  DB7176700
HS Code  2934302300
Toxicity LD50 in mice (mg/kg): 33 i.v.; 611 s.c.; 346 orally (Maruyama)

Mesoridazine Besylate price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 1393005 Mesoridazine besylate United States Pharmacopeia (USP) Reference Standard 32672-69-8 25MG $439 2024-03-01 Buy
Sigma-Aldrich 1393005 Mesoridazine besylate United States Pharmacopeia (USP) Reference Standard 32672-69-8 250mg $431 2022-05-15 Buy
TRC M225755 Mesoridazine besylate 32672-69-8 500mg $1155 2021-12-16 Buy
American Custom Chemicals Corporation MTB0000023 MESORIDAZINE BENZENESULFONATE 95.00% 32672-69-8 1G $1871.1 2021-12-16 Buy
Medical Isotopes, Inc. 59647 Mesoridazine besylate 32672-69-8 100mg $625 2021-12-16 Buy
Product number Packaging Price Buy
1393005 25MG $439 Buy
1393005 250mg $431 Buy
M225755 500mg $1155 Buy
MTB0000023 1G $1871.1 Buy
59647 100mg $625 Buy

Mesoridazine Besylate Chemical Properties,Uses,Production

Originator

Serentil,Sandoz,US,1970

Uses

Mesoridazine (M225755) Besylate is an antipsychotic.

Uses

antpsychotic

Definition

ChEBI: The benzenesulfonate salt of mesoridazine prepared using equimolar amounts of mesoridazine and benzenesulfonic acid.

Manufacturing Process

10.0 g of 3-methylmercapto phenothiazine and 17.5 cc of acetic acid anhydride are refluxed for 8 hours from an oil bath maintained at a temperature of 180°C. After concentration of the solution the residue is crystallized from ethanol. The pure 3-methylmercapto-10-acetyl phenothiazine melts at 89° to 91°C. For the purpose of oxidation 5.0 g of 3- methylmercapto-10-acetyl phenothiazine are dissolved in 50 cc of ethanol, refluxed from an oil bath maintained at 120°C and 1.6 cc of a 40% hydrogen peroxide solution are then added dropwise in the course of 30 minutes.
Heating is continued for another 5 hours and the reaction mixture is concentrated after 50 cc of water have been added. The residue is taken up in 40 cc of benzene and the benzene layer washed with 10 cc of water. After having been concentrated, the residue, crude 3-methylsulfinyl-10-acetyl phenothiazine, is dissolved in 55 cc of a 90% methanol solution for splitting off the acetyl group and, after 2.9 g of potassium carbonate have been added, it is boiled for 2 hours under reflux on an oil bath kept at a temperature of 120°C. After concentration, the residue is taken up in 50 cc of chloroform, the chloroform layer is washed with a total of 25 cc of water, dried over potassium carbonate, filtered and concentrated. After twice crystallizing the residue, each time from 50 cc of ethanol, analytically pure 3-methylsulfinyl phenothiazine (MP 193° to 195°C) is obtained.
A mixture of 10.0 g of 3-methylsulfinyl phenothiazine (MP 193° to 195°C), 6.1 g of finely powdered sodium hydroxide and 125 cc of toluene is boiled for 1 hour under reflux with a water separator on an oil bath kept at a temperature of 150°C, while the mixture is stirred. Without interrupting the boil a solution of 7.0 g of 2-(N-methyl-piperidyl-2')-1-chloroethane (BP 84°C/10 mm Hg) in 10 cc of toluene is added dropwise in the course of 1 hour, after which boiling is continued for another 3 hours. When the reaction mixture has cooled it is first washed with 25 cc of water three times and then extracted with 75 cc of a 15% aqueous tartaric acid solution. The tartaric acid extract is shaken out with 25 cc of benzene, 20 cc of concentrated caustic soda are added until the phenolphthalein reaction is alkaline, and the separated oily base is taken up in a total of 150 cc of benzene.
After having been washed with 50 cc of water the benzene layer is dried over potassium carbonate, filtered, allowed to stand over 10 g of alumina for about 1? hours for partial decolorization, filtered again and concentrated under reduced pressure. The oily base which remains as a residue is directly converted into the tartrate. A solution cooled to 0°C, of 6.50 g of the free base in 100 cc of acetic acid ethyl ester is thoroughly shaken and poured into an ice cold solution of 2.66 g of tartaric acid in 410 cc of acetic acid ethyl ester. The precipitated, analytically pure, tartrate of 3-methylsulfinyl-10-[2'-Nmethyl-piperidyl-2')-ethyl-l']-phenothiazine melts at 115° to 120°C (foam formation) and sinters above 80°C. The base is reacted with benzene sulfonic acid in a suitable solvent to give the besylate.

brand name

Serentil (Novartis).

Therapeutic Function

Tranquilizer

General Description

Mesoridazine besylate,10-[2-(methyl-2-piperidyl)ethyl]-2-(methylsulfinyl)phenothiazinemonobenzenesulfonate (Serentil), shares manyproperties with thioridazine. However, no pigmentaryretinopathy has been reported.

Mesoridazine Besylate Preparation Products And Raw materials

Global( 43)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Dideu Medichem Co. Ltd
+86-029-81138252 +86-18789408387 1057@dideu.com China 3958 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 32165 58
TargetMol Chemicals Inc.
support@targetmol.com United States 38632 58
Aladdin Scientific
+1-+1(833)-552-7181 sales@aladdinsci.com United States 57505 58
Sinopharm Chemical Reagent Co,Ltd. 86-21-63210123 sj_scrc@sinopharm.com China 9815 79
Shanghai TaoSu Biochemical Technology Co., Ltd. 021-33632979 info@tsbiochem.com China 8065 58
Shanghai Rechem science Co., Ltd. 21-31433387 15618786686 sales@rechemscience.com China 3002 58
Beijing Solarbio Science & Tecnology Co., Ltd. 010-50973186 4009686088 3193328036@qq.com China 18338 68
Aikon International Limited 025-66113011 18112977050 cb6@aikonchem.com China 15494 58
Angel Pharmatech, Ltd. 17317130613 3358272972@qq.com China 3251 58

View Lastest Price from Mesoridazine Besylate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Mesoridazine Besylate pictures 2024-11-19 Mesoridazine Besylate
32672-69-8
US $132.00-70.00 / mg 99.58% 10g TargetMol Chemicals Inc.
Mesoridazine Besylate pictures 2024-07-25 Mesoridazine Besylate
32672-69-8
US $1.00 / KG 1KG 99% 20T Shaanxi Dideu Medichem Co. Ltd

Mesoridazine Besylate Spectrum

SERENTIL benzenesulfonicacid,compd.with10-(2-(1-methyl-2-piperidinyl)ethyl)-2-(meth nc123 ylsulfinyl)ethyl)-10h-phenothiazine(1:1) MESORIDAZINE BENZENESULFONATE MESORIDAZINE BESYLATE 10-[2-(1-METHYL-2-PIPERIDINYL)ETHYL]-2-(METHYLSULFINYL)-10H-PHENOTHIAZINE Mesoridazine Besylate (250 mg) Mesoridazine Besylate (1393005) Mesoridazine Besilate (10-[2-[(2RS) 10-(2-(1-Methylpiperidin-2-yl)ethyl)-2-(methylsulfinyl)-10H-phenothiazine benzenesulfonate Thioridazine Hydrochloride EP Impurity B as Besilate Thioridazine Hydrochloride Impurity B as Besilate Thioridazine EP Impurity B Besylate (Mesoridazine Besylate) Mesoridazine benzenesulfonate|||Serentil 32672-69-8 C21H26N2OS2C6H6SO3 C27H32N2O4S3 SERENTIL