Promazine

Promazine Basic information
Product Name:Promazine
Synonyms:PHENOTHIAZINE,10-(3-(DIMETHYLAMINO)PROPYL)-;N,N-Dimethyl-3-(10H-phenothiazin-10-yl)propan-1-amine;dimethyl(3-phenothiazin-10-ylpropyl)amine;A-145;RP-3276;Wy-1094;Promazine;N,N-dimethyl-3-phenothiazin-10-yl-propan-1-amine
CAS:58-40-2
MF:C17H20N2S
MW:284.4191
EINECS:2003820
Product Categories:
Mol File:58-40-2.mol
Promazine Structure
Promazine Chemical Properties
Melting point 25°C
Boiling point bp0.3 203-210°
density 1.1256 (rough estimate)
refractive index 1.6000 (estimate)
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pkapKa 9.4(H2O,t =24±1) (Uncertain)
color Off-White to Pale Beige
Water Solubility 14.22mg/L(24 ºC)
Stability:Hygroscopic
NIST Chemistry ReferencePromazine(58-40-2)
Safety Information
Hazardous Substances Data58-40-2(Hazardous Substances Data)
ToxicityLD50 oral in rat: 350mg/kg
MSDS Information
Promazine Usage And Synthesis
Usesntipsychotic.
UsesPromazine is an antipsychotic and a tranquilizer.
UsesIn psychiatric practice, promazine is used in minor cases of psychomotor excitement in schizophrenics, in paranoid and manic-depressive conditions, for neurosis, alcoholic psychosis, and others. It is sometimes used in anesthesiological practice.
DefinitionChEBI: A phenothiazine deriative in which the phenothiazine tricycle has a 3-(dimethylaminopropyl) group at the N-10 position.
Brand nameSparine (Baxter Healthcare); Sparine (Wyeth).
General DescriptionPromazine, 10-[3-(dimethylamino) propyl-(phenothiazine monohydrochloride (Sparine), was introducedinto antipsychotic therapy after its 2-chloro-substitutedrelative. The 2H-substituent vis-à-vis the 2Clsubstituent gives a milligram potency decrease as an antipsychotic,as encompassed in Gordon’s rule. Tendency toEPS is also lessened, which may be significant, especially ifit is decreased less than antipsychotic potency.
SynthesisPromazine, 10-(3-dimethylaminopropyl)phenothiazine (6.1.1), is prepared by the alkylation of phenothiazine with 3-dimethylaminopropylchloride in the presence of sodium amide [1¨C3].

Synthesis_58-40-2

Promazine Preparation Products And Raw materials
Promethazine hydrochloride Dacthal Trifluoperazine dihydrochloride Chlorpromazine hydrochloride IMIPRAMINE N,N-Dimethylcyclohexylamine ETHANE DIOXOPROMETHAZINE Promazine Dimethyl sulfide THIORIDAZINE HYDROCHLORIDE N,N-Dimethylallylamine Dimethyl sebacate Dimethyl ether acepromazine DIOXOPROMETHAZINE HCL PROMETHAZINE Dimethyl sulfate

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