55389-75-8

Basic information

• Product Name: BIS-(3,4-DIMETHYL-PHENYL)-AMINE
• Synonyms: Bis(3,4-dimethylphenyl)amine;4-diMethyl-phenyl)-aMine;Bis-(3;N-(3,4-diMethylphenyl)-2,4-diMethylaniline;Bis-(3,4-dimethylphenyl);Benzenamine,N-(3,4-dimethylphenyl)-3,4-dimethyl-;N-(3,4-dimethylphenyl)-3,4-dimethylaniline;N-(3,4-dimethylphenyl)
• CAS NO: 55389-75-8
• Molecular Formula: C₁₆H₁₉N
• Molecular Weight: 225.33
• EINECS: 200-258-5
• Mol File: 55389-75-8.mol
• Article Data: 3

Chemical Properties

• Melting Point: 110 °C
• Boiling Point: 367 °C at 760 mmHg
• Flash Point: 184.6 °C
• Appearance: /
• Density: 1.021 g/cm³
• Vapor Pressure: 1.41E-05mmHg at 25°C
• Refractive Index: 1.594
• Storage Temp.: 2-8°C(protect from light)
• PKA: 2.06±0.50(Predicted)
• CAS DataBase Reference: BIS-(3,4-DIMETHYL-PHENYL)-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: BIS-(3,4-DIMETHYL-PHENYL)-AMINE(55389-75-8)
• EPA Substance Registry System: BIS-(3,4-DIMETHYL-PHENYL)-AMINE(55389-75-8)

Safety Data

• Hazardous Substances Data: 55389-75-8(Hazardous Substances Data)

Usage

General Description

BIS-(3,4-DIMETHYL-PHENYL)-AMINE is a chemical compound also known as 3,3’-Dimethyl-4,4’-diaminodiphenylmethane. It is a diamine derivative of diphenylmethane, which is commonly used in the production of polyurethane and epoxy resins as a curing agent. This chemical is also used as a crosslinking agent in the manufacturing of adhesives, coatings, and sealants. It is known for its high reactivity and ability to improve the mechanical and thermal properties of polymer materials, making it a valuable component in various industrial applications. However, it is important to handle this chemical with caution and follow safety protocols due to its potential health hazards if mishandled.

InChI:InChI=1/C16H19N/c1-11-5-7-15(9-13(11)3)17-16-8-6-12(2)14(4)10-16/h5-10,17H,1-4H3

Upstream product

• 583-71-1 4-bromo-o-xylene 
• 95-65-8 3,4-Dimethylphenol 
• 576-23-8 2,3-dimethylbromobenzene 

Downstream Products

• 1361571-14-3 N,N,N',N'-tetrakis-(3,4-dimethyl-phenyl)-anthracene-9,10-diamine 
• 1336947-48-8 N,N,N',N'-tetrakis(3,4-dimethylphenyl)-9,9'-spirobifluorene-2,7-diamine 
• 1259383-66-8 C₂₇H₃₇NO₂Si₂ 
• 1087093-99-9 3-iso-propyl-N₆,N₆,N₁₂,N₁₂-tetrakis-(3,4-dimethylphenyl)-chrysene-6,12-diamine 
• 215390-23-1 (Z)-1-(4-iso-propylstyryl)naphthalene 

Relevant articles and documents

Direct Synthesis of Diphenylamines from Phenols and Ammonium Formate Catalyzed by Palladium

Arylamines are commercially and synthetically useful compounds with a wide variety of applications. Their preparation has been traditionally achieved using metal-catalyzed C?N coupling reactions with aryl halides. In this work, 17 different diarylamines are prepared from phenols by using ammonium formate as the aminating reagent. Phenolic compounds are more desirable feedstocks, owing to their availability from lignin, making them valuable biorenewable alternatives to aryl halides. Ammonium formate is found to be a convenient surrogate for ammonia and a useful aminating reagent for phenols. Diarylamine products are obtained in good to excellent yields while only water and CO2 are generated as byproducts of the transformation.

Triarylamine compounds useful in electrophotographic photoreceptors

A triarylamine compound useful as a charge transport material of an electrophotographic photoreceptor, which represented by formula (I) STR1 wherein Ar1 and Ar2 each represents a phenyl group or a condensed ring group.