58047-42-0

Basic information

• Product Name: 4-Bromo-4',4''-dimethyltriphenylamine
• Synonyms: (4-Bromo-phenyl)-di-p-tolyl-amine;4-BROMO-4'',4''-DIMETHYLTRIPHENYLAMINE;4-BROMO-4'',4''-DIMETHYLTRIPHENYLAMINE,95.0+%(GC);4-Bromo-N,N-di-p-tolylaniline;4-Bromo-N,N-dip-tolylbenzenamine ,97%;4-broMo -4',4''- twoMethyl threeaniline;BDMTPA;4-Bromo-N,N-bis(4-methylphenyl)benzenamine
• CAS NO: 58047-42-0
• Molecular Formula: C₂₀H₁₈BrN
• Molecular Weight: 352.27
• Mol File: 58047-42-0.mol
• Article Data: 16

Chemical Properties

• Melting Point: 102 °C
• Boiling Point: 459.927 °C at 760 mmHg
• Flash Point: 231.956 °C
• Appearance: /
• Density: 1.308 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.643
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: -2.82±0.50(Predicted)
• CAS DataBase Reference: 4-Bromo-4',4''-dimethyltriphenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Bromo-4',4''-dimethyltriphenylamine(58047-42-0)
• EPA Substance Registry System: 4-Bromo-4',4''-dimethyltriphenylamine(58047-42-0)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/37/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 58047-42-0(Hazardous Substances Data)

Usage

Chemical Properties

off-white powder

InChI:InChI=1/C20H18BrN/c1-15-3-9-18(10-4-15)22(19-11-5-16(2)6-12-19)20-13-7-17(21)8-14-20/h3-14H,1-2H3

Upstream product

• 108-86-1 bromobenzene 
• 589-87-7 1,4-bromoiodobenzene 
• 135-88-6 N-Phenyl-2-naphthylamine 
• 620-93-9 di-p-tolylamine 
• 20440-95-3 N-phenyl-di-p-tolylamine 
• 624-31-7 4-tolyl iodide 
• 106-40-1 4-bromo-aniline 

Downstream Products

• 438633-03-5 3-bromo-5-{4-[bis(4-methylphenyl)amino]phenyl}-2-methylthiophene 
• 528610-00-6 4-methyl-N-(4-methylphenyl)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)amine 
• 1006708-00-4 N-(1-phenylpyrazole-3-yl)-N-(1-phenyl-5-methylpyrazole-3-yl)-4-(di(p-tolyl)amino)aniline 
• 1338829-30-3 2-[4-(di-p-tolylamino)phenyl]-3H-indene-5-carbonitrile 
• 1338829-34-7 2-[4-(di-p-tolylamino)phenyl]-3H-indene-5-carbaldehyde 
• 1338829-26-7 2-cyano-3-[2-(4-(di-p-tolylaminophenyl))-3H-inden-5-yl]acrylic acid 
• 1376711-81-7 4,4′-dimethyl-4′′-tributylstannyltriphenylamine 
• 1417779-55-5 4-(3,4-ethylenedioxythiophen-2-yl)-N,N-bis(4-methylphenyl)aniline 
• 1374310-76-5 4-(2-(tributylstannyl)thiophene-5-yl)-N,N-bis(4-methylphenyl)aniline 
• 1376711-83-9 6-{5-{4-[N,N-bis(4-methylphenyl)amino]phenyl}thiophene-2-yl}-4H-cyclopenta[2,1-b:3,4-b']dithiophen-4-one-2-carbaldehyde 
• 1376711-86-2 2-cyano-3-{6-{2-{4-[N,N-bis(4-methylphenyl)amino]phenyl}thiophene-5-yl}-4H-cyclopenta[2,1-b:3,4-b']dithiophen-4-one-2-yl}acrylic acid 
• 1376711-84-0 6-{5-{4-[N,N-bis(4-methylphenyl)amino]phenyl}-3,4-ethylenedioxythiophene-2-yl}-4H-cyclopenta[2,1-b:3,4-b']dithiophen-4-one-2-carbaldehyde 
• 1376711-79-3 6-{4-[N,N-bis(4-methylphenyl)amino]phenyl}-4H-cyclopenta[2,1-b:3,4-b']dithiophen-4-one-2-carbaldehyde 
• 1398122-58-1 2-bromo-7-(4-(N,N-di-p-tolylamino)phenyl)-9-oxo-9H-fluorene 

Relevant articles and documents

Hole transport material containing isoindigo compound as well as preparation method and application thereof

The hole transport material takes isoindigo-containing compound as a core, the alkyl chain is introduced to improve the solubility, different donor groups are introduced to regulate the energy level, and the hole transport capacity is improved. The synthesized hole transport and transmission material is low in cost and good in hole transport capacity, and has high application value in the field of solar cells. The hole transport material has good hole transport performance and good solubility, is applied to a perovskite solar cell as a hole transport layer, and improves the photoelectric conversion efficiency of the solar cell.

For solution treated organic solar cell of low band gap containing ruthenium complex

This invention relates to a class of ruthenium(II) bis(aryleneethynylene) complexes for use in bulk heterojunction (BHJ) solar cell devices, and the method of synthesizing thereof. This invention also relates to a BHJ solar cell device comprising the ruth

Substituted triphenylamines as building blocks for star shaped organic electronic materials

A versatile synthetic protocol toward a series of various substituted triphenylamine derivatives serving as building blocks for organic electronic materials was developed. Key steps during synthesis were either Ullmann condensations or nucleophilic aromatic substitutions giving rise to structural modification of triphenylamines and their electronic nature. In turn, these scaffolds were exemplarily attached to a dendritic tris(2-thienyl)benzene core affording star shaped organic semiconducting materials which were characterized regarding their photo-physical, electro-chemical and thermal properties. A strong influence of the substituent's nature on both photo-physical and morphological thin film characteristic of star shaped target compounds was observed. The applicability of these materials in organic electronic devices was demonstrated in an organic field effect transistor configuration yielding a hole mobility of nearly 10-3 cm2 V-1 s-1. The performance of the materials can be correlated to the substituents applied. This journal is