3926-64-5

Basic information

• Product Name: 2-hydroxypromazine
• Synonyms: 2-hydroxypromazine;10-[3-(Dimethylamino)propyl]-10H-phenothiazin-2-ol;8-Hydroxypromazine
• CAS NO: 3926-64-5
• Molecular Formula: C₁₇H₂₀N₂OS
• Molecular Weight: 300.4185
• Product Categories: Amines;Aromatics;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;Sulfur & Selenium Compounds;Amines, Aromatics, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals, Sulfur & Selenium Compounds
• Mol File: 3926-64-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 479.4°Cat760mmHg
• Flash Point: 243.8°C
• Appearance: /
• Density: 1.204g/cm³
• Vapor Pressure: 8.14E-10mmHg at 25°C
• Refractive Index: 1.639
• Storage Temp.: -20°C Freezer
• Solubility: Chloroform (Slightly, Heated), Methanol (Slightly, Sonicated)
• CAS DataBase Reference: 2-hydroxypromazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-hydroxypromazine(3926-64-5)
• EPA Substance Registry System: 2-hydroxypromazine(3926-64-5)

Safety Data

• Hazardous Substances Data: 3926-64-5(Hazardous Substances Data)

Usage

Uses

A metabolite of Promazine (P756300).

InChI:InChI=1/C17H20N2OS/c1-18(2)10-5-11-19-14-6-3-4-7-16(14)21-17-9-8-13(20)12-15(17)19/h3-4,6-9,12,20H,5,10-11H2,1-2H3

Upstream product

• 69-09-0 chlorpromazine hydrochloride 
• 101884-26-8 2-benzoyloxy-10H-phenothiazine 
• 109-54-6 3-(Dimethylamino)propyl chloride 
• 50-53-3 2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine 

Downstream Products

• 22541-69-1 plutonium (5+) 

Relevant articles and documents

Photochemistry in Micelles as a Model for the in vivo Phototoxicity of Chlorpromazine

The photochemical reactivity of chlorpromazine has been studied in an oxygenated solution containing micelles.The photochemical dehalogenation reaction which had previously only been observed in oxygen-free solutions was found to predominate.The relevance of this photoreaction and the micelle as a model for the in vivo phototoxicity of chlorpromazine is discussed.

Cation Radicals of Phenothiazines. Part 4. Electron Transfer Between Aquamanganase(III) and N-Alkylphenothiazines

The kinetics of electron transfer between aquamanganase(III) and N-alkylphenothiazines, giving rise to the corresponding cation radicals, has been investigated in the range 0.20-1.50 mol dm-3 HClO4 at different temperatures.The main reaction path has been assigned to the unhydrolysed species Mn(3+)(aq), and there is a dependence of the rate constants on the corresponding reduction potentials.