76-82-4

Basic information

• Product Name: (4-amino-3-methyl-phenyl)-bis(4-aminophenyl)methanol
• Synonyms: (4-amino-3-methyl-phenyl)-bis(4-aminophenyl)methanol
• CAS NO: 76-82-4
• Molecular Formula: C₂₀H₂₁N₃O
• Molecular Weight: 0
• Mol File: 76-82-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 597.7°C at 760 mmHg
• Flash Point: 315.3°C
• Appearance: /
• Density: 1.26g/cm³
• Vapor Pressure: 3.92E-15mmHg at 25°C
• Refractive Index: 1.706
• CAS DataBase Reference: (4-amino-3-methyl-phenyl)-bis(4-aminophenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (4-amino-3-methyl-phenyl)-bis(4-aminophenyl)methanol(76-82-4)
• EPA Substance Registry System: (4-amino-3-methyl-phenyl)-bis(4-aminophenyl)methanol(76-82-4)

Safety Data

• Hazardous Substances Data: 76-82-4(Hazardous Substances Data)

Usage

General Description

The chemical (4-amino-3-methyl-phenyl)-bis(4-aminophenyl)methanol, also known as Bis-amino-phenyl-methanol or 4-(4-(4-aminophenyl)-3-methylphenylamino)benzyl alcohol, is a compound with a complex molecular structure. It is a bisphenol derivative with two amino groups and a benzyl alcohol moiety. This chemical compound has potential applications in the field of organic synthesis and pharmaceuticals due to its unique structure and reactivity. It may also be used in the production of polymers and other industrial processes. However, further research is needed to fully understand its properties and potential uses.

InChI:InChI=1/C20H21N3O/c1-13-12-16(6-11-19(13)23)20(24,14-2-7-17(21)8-3-14)15-4-9-18(22)10-5-15/h2-12,24H,21-23H2,1H3

Upstream product

• 63861-53-0 Fuchsin 
• 7778-39-4 orthoarsenic acid 
• 62-53-3 aniline 
• 95-68-1 2,4-Xylidine 
• 106-49-0 p-toluidine 
• 95-53-4 o-toluidine 
• 632-99-5 4-[(4-aminophenyl)(4-imino-2,5-cyclohexadien-1-ylidene)methyl]-2-methylaniline hydrochloride 
• 7732-18-5 water 
• 14337-01-0 hydroxide 
• 151-21-3 sodium dodecyl-sulfate 
• 57-09-0 cetyltrimethylammonim bromide 
• 142-04-1 aniline hydrochloride 
• 603-27-0 (4-amino-3-methyl-phenyl)-bis-(4-amino-phenyl)-methane 

Downstream Products

• 611-98-3 4,4'-diaminobenzophenone 
• 95-53-4 o-toluidine 
• 611-99-4 4,4'-Dihydroxybenzophenone 
• 121125-68-6 4,4'-diamino-3-methyl-benzophenone 
• 7664-41-7 ammonia 
• 108-95-2 phenol 
• 62-53-3 aniline 
• 35675-66-2 4-(4,4'-dihydroxy-3-methyl-benzhydrylidene)-cyclohexa-2,5-dienone 
• 4468-55-7 (4-amino-3-methyl-phenyl)-bis-(4-amino-phenyl)-acetonitrile 

Relevant articles and documents

Kinetics of reduction of triaminotolyldiphenylmethane chloride (rosaniline hydrochloride) by hydroxide ions in aqueous medium

Kinetics and mechanism of reduction of rosaniline hydrochloride (RH) by hydroxide ions have been studied in aqueous medium at 30°C at ionic strength of 1.0 mol dm-3 (NaCl). The reduction follows a second order kinetics and it conforms to the rate law: -d/dt [RH] = k2 [RH][OH-] and k2 is found to be 1.84 ± 0.04 × 102 mol dm-3 min-1. The rate of reaction is not sensitive to changes in dielectric constant of the medium and free radicals have not been detected in the reaction. The rate of reaction decreased with increase in ionic strength. The results from our spectroscopic investigations and Michaelis-Menten analysis do not show any evidence for an intermediate of significant stability. The outersphere mechanism is, therefore, postulated for this reaction.