ACETOPHENAZINE MALEATE (200 MG)

ACETOPHENAZINE MALEATE (200 MG) Basic information
Product Name:ACETOPHENAZINE MALEATE (200 MG)
Synonyms:Acetophenazine dimaleate salt;ketone,10-(3-(4-(2-hydroxyethyl)-1-piperazinyl)propyl)phenothiazin-2-ylmethyl;ketone,10-(3-(4-(2-hydroxyethyl)-1-piperazinyl)propyl)phenothiazin-2-ylmethyl,dimaleate;sch6673;tindal;ACETOPHENAZINE MALEATE (200 MG);2-acetyl-10-[3-[4-(2-hydroxyethyl)piperazinyl]propyl]-10H-phenothiazine dimaleate;ACETOPHENZAINEMALEATE
CAS:5714-00-1
MF:C53H64N6O11S2
MW:1025.23886
EINECS:227-202-3
Product Categories:Amines;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Sulfur & Selenium Compounds
Mol File:5714-00-1.mol
ACETOPHENAZINE MALEATE (200 MG) Structure
ACETOPHENAZINE MALEATE (200 MG) Chemical Properties
Melting point 167-168.5°
storage temp. Hygroscopic, Refrigerator, under inert atmosphere
solubility DMSO (Slightly), Methanol (Slightly)
form neat
color Yellow to Orange
Stability:Hygroscopic
Safety Information
Hazard Codes Xi
Risk Statements 36
Safety Statements 26
RTECS OB4180000
ToxicityLD50 orally in rats: 433 mg/kg (Schafer)
MSDS Information
ACETOPHENAZINE MALEATE (200 MG) Usage And Synthesis
OriginatorTindal ,Schering ,US ,1961
UsesAntipsychotic.
DefinitionChEBI: A maleate salt obtained by combining acetophenazine with two molar equivalents of maleic acid.
Manufacturing ProcessThe requisite intermediate, 10-(3-chloropropyl)-2-acetylphenothiazineis prepared as follows: To a suspension of sodium amide (from 3 grams of sodium) in 300 ml of liquid ammonia is added 30 grams of 2- acetylphenothiazine. After stirring for one hour, there is added 19 grams of 1- bromo-3-chloropropane. The ammonia is allowed to evaporate and the residue is diluted with 200 ml of water. The mixture is extracted with ether and the ether solution is dried over anhydrous sodium sulfate, filtered and concentrated.
The residue consists of crude 10-(3-chloropropy1)-2-acetylphenothiazine as a viscous oil and is used in the next step without further purification. The crude base obtained from the reaction of 10-(3-chloropropyl)-2-acetylphenothiazine with 1-(2-hydroxyethyl)piperazine is purified by conversion to its dimaleate salt, MP 167-168.5°C from ethanol.
Brand nameTindal (Schering).
Therapeutic FunctionTranquilizer
Safety ProfilePoison by ingestion, intraperitoneal,and intravenous routes. Severe eye irritant.
ACETOPHENAZINE MALEATE (200 MG) Preparation Products And Raw materials
Raw materialsMaleic acid
Phenothiazine Prochlorperazine ACETOPHENAZINE

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