Levomepromazine hydrochloride
Synonym(s):(R)-3-(2-Methoxy-10H-phenothiazin-10-yl)-N,N,2-trimethylpropylamine hydrochloride
- CAS NO.:1236-99-3
- Empirical Formula: C19H24N2OS.ClH
- Molecular Weight: 364.93
- EINECS: 214-978-3
- SAFETY DATA SHEET (SDS)
- Update Date: 2026-04-21 10:31:43
What is Levomepromazine hydrochloride?
Originator
Levoprome ,Lederle,US,1966
The Uses of Levomepromazine hydrochloride
Analgesic (central nervous system depressant).
Definition
ChEBI: Levomepromazine hydrochloride is a member of phenothiazines.
Manufacturing Process
95% sodamide (2.33 g) is added to a boiling solution of 3- methoxyphenthiazine (12 g) in anhydrous xylene (150 cc) and the mixture is heated with agitation under reflux for 1? hours. A solution of 1- dimethylamino-2-methyl-3-chloropropane (8.2 g) in anhydrous xylene (90 cc) is then run in over a period of 45 minutes while the reaction temperature is maintained and heating under reflux is continued for 18 hours.
After cooling, the reaction mixture is agitated with a mixture of water (40 cc) and a normal solution of methanesulfonic acid (70 cc), the xylene layer is removed and the acid liquors are washed with ether (200 cc). The aqueous phase is then made alkaline with sodium hydroxide (d = 1.33; 10 cc) and the liberated base is extracted with ether. The ethereal solution is dried over anhydrous potassium carbonate and concentrated at normal pressure. On distillation of the residue under reduced pressure 3-(3-methoxy-10- phenthiazinyl)-2-methyl-1-dimethylaminopropane (11.3 g) is obtained, MP 103°C, BP 182° to 191°C/0.15 mm Hg. The hydrochloride prepared in isopropanol melts at about 90°C.
brand name
Nozinan (Aventis).
Therapeutic Function
Analgesic
Properties of Levomepromazine hydrochloride
| storage temp. | 2-8°C |
| form | neat |
Safety information for Levomepromazine hydrochloride
Computed Descriptors for Levomepromazine hydrochloride
New Products
Pentadecanoic acid 3-Bromophenylacetic acid 3-AMINO-3-(2-FLUORO-PHENYL)-PROPIONIC ACID Hendecanoic acid 2-Amino-5-cyanopyridine 2-Bromo-5-cyanopyridine 4-(4-(Dimethylamino)-1-(4-fluorophenyl)-1-hydroxybutyl)-3-(hydroxymethyl)benzonitrile 3′-Hydroxyacetophenone 5-fluoro-1,3-benzodioxole 5-Bromo-4-chloro-3-indolyl-β-D-galactopyranoside Tetracaine Hydrochloride Ep Grade 2,2,2-Trichloroethyl chloroformate 2-Bromo-6-fluoroaniline 2-Amino-4-phenyl-thiazole 4-Chloro-2-methyl quinoline 2-(Chloromethyl) quinazolin-4(3H)-one 5-Phenyl-[1,3,4]-thiadiazol-2-amine 2-Chloro-6-nitro benzothiazole N-(4-Bromophenyl)-2-chloroacetamide 6-Isopropylpicolinonitrile N-Methyl-3,5-dinitro-2-pyridinamine Phenyl-boronic acid-d5 10,11-Dihdyro-10-oxo-5H-dibenz[b,f]azepine-5-carboxamide-d4 5-(2,4-difluorophenyl)oxazolidin-2-oneRelated products of tetrahydrofuran



![(-)-10-(3-[DIMETHYLAMINO]-2-METHYLPROPYL)-2-METHOXY-PHENOTHIAZINE MALEATE SALT](https://img.chemicalbook.in/CAS/GIF/60-99-1.gif)




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