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
- Chlorpromazine Impurity 4
- A-145
- RP-3276
- Wy-1094
- Promazine
- CAS:
- 58-40-2
- MF:
- C17H20N2S
- MW:
- 284.4191
- EINECS:
- 2003820
- Mol File:
- 58-40-2.mol
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)
- pka
- pKa 9.4(H2O,t =24±1) (Uncertain)
- form
- Solid
- color
- Off-White to Pale Beige
- Water Solubility
- 14.22mg/L(24 ºC)
- Stability:
- Hygroscopic
- NIST Chemistry Reference
- Promazine(58-40-2)
Safety Information
- Hazardous Substances Data
- 58-40-2(Hazardous Substances Data)
- Toxicity
- LD50 oral in rat: 350mg/kg
Promazine Usage And Synthesis
Uses
ntipsychotic.
Uses
In 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.
Uses
Promazine is an antipsychotic and a tranquilizer.
Definition
ChEBI: A phenothiazine deriative in which the phenothiazine tricycle has a 3-(dimethylaminopropyl) group at the N-10 position.
brand name
Sparine (Baxter Healthcare); Sparine (Wyeth).
General Description
Promazine, 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.
Synthesis
Promazine, 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].
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