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Promazine

CAS No.
58-40-2
Chemical Name:
Promazine
Synonyms
A-145;Wy-1094;RP-3276;Esparin;Promazine;NSC 31447;Sinophenin;Chlorpromazine-003;Promazine USP/EP/BP;Promazine Dimer Impurity
CBNumber:
CB5875452
Molecular Formula:
C17H20N2S
Molecular Weight:
284.4191
MDL Number:
MFCD00242576
MOL File:
58-40-2.mol
Last updated:2023-05-15 10:43:35

Promazine 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
pka pKa 9.4(H2O,t =24±1) (Uncertain)
color Off-White to Pale Beige
Water Solubility 14.22mg/L(24 ºC)
Stability Hygroscopic
FDA UNII O9M39HTM5W
ATC code N05AA03
NIST Chemistry Reference Promazine(58-40-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P330-P501
Hazardous Substances Data 58-40-2(Hazardous Substances Data)
Toxicity LD50 oral in rat: 350mg/kg

Promazine price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0007567 N,N-DIMETHYL-3-PHENOTHIAZIN-10-YL-PROPAN-1-AMINE 95.00% 58-40-2 5MG $501.88 2021-12-16 Buy
Product number Packaging Price Buy
API0007567 5MG $501.88 Buy

Promazine Chemical Properties,Uses,Production

Uses

ntipsychotic.

Uses

Promazine is an antipsychotic and a tranquilizer.

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.

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].

Synthesis_58-40-2

Promazine Preparation Products And Raw materials

Raw materials

Preparation Products

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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 N,N-dimethyl-3-phenothiazin-10-ylpropan-1-amine Chlorpromazine impurity 1 Chlorpromazine Impurity 4 Chlorpromazine Impurity 3(Chlorpromazine EP Impurity C) Chlorpromazine-003 10H-Phenothiazine-10-propanamine, N,N-dimethyl- Promazine USP/EP/BP Chlorpromazine hydrochloride EP Impurity C Esparin NSC 31447 Sinophenin Promazine Dimer Impurity 58-40-2