N,N'-Bis(3-methylphenyl)-N,N'-bis(phenyl)benzidine Chemical Properties

Melting point:

169°C

Boiling point:

680.1±55.0 °C(Predicted)

Density 

1.37 g/cm3

vapor pressure 

3.356Pa at 25℃

storage temp. 

Sealed in dry,Room Temperature

Water Solubility 

Insoluble in water

form 

Powder

pka

-2.40±0.60(Predicted)

Stability:

Stable. Incompatible with strong oxidizing agents.

LogP

4.29 at 20℃ and pH6.3-6.5

Surface tension

72.3mN/m at 242μg/L and 21.9℃

CAS DataBase Reference

65181-78-4(CAS DataBase Reference)

EPA Substance Registry System

[1,1'-Biphenyl]-4,4'-diamine, N,N'-bis(3-methylphenyl)-N,N'-diphenyl- (65181-78-4)

color 

White powder/crystals

Absorption

λmax?352 nm?in THF

Safety Information

Hazard Codes 

N

Risk Statements 

36/37/38-51/53

Safety Statements 

26-36/37/39-61

RIDADR 

3077

WGK Germany 

2

HazardClass 

9

PackingGroup 

III

HS Code 

29215900

N,N'-Bis(3-methylphenyl)-N,N'-bis(phenyl)benzidine Usage And Synthesis

Applications

N,N′-Bis(3-methylphenyl)-N,N′-diphenylbenzidine, commonly abbreviated as TPD, is widely used as hole transport materials in organic electronic devices.
TPD is also used as a blue-violet light emitting material or host material on the phosphorescence organic light emitting diodes for its wide energy band is about 3.2 eV with highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) 5.5 eV and 2.3 eV respectively.

Uses

Hole transport material for electrophotographic photoconductor in xerography.

Description

N,N′-Bis(3-methylphenyl)-N,N′-diphenylbenzidine, commonly abbreviated as TPD,?is widely used as hole transport materials in organic electronic devices.

Chemical Properties

solid

Uses

Organic photoconductor. Hole transporter.

Synthesis

General procedure for the synthesis of N,N'-diphenyl-N,N'-bis(3-methylphenyl)-1,1'-biphenyl-4,4'-diamine from 4,4'-dibromobiphenyl and 3-methyldiphenylamine: under argon protection, 3.0 g (30 mmol) of sodium tert-butoxide, 217 mg (0.5 mmol) of IPr-HCl (Compound No.1), 45 mg ( 0.2 mmol) palladium(II) acetate, 3.67 g (20 mmol) 3-methyldiphenylamine, 3.2 g (10 mmol) 4,4'-dibromobiphenyl, and 30 ml of toluene were added to a 50 ml three-necked flask fitted with a stirrer, a condenser tube, a thermometer, and a gas introduction tube. The reaction mixture was heated to 130°C in an oil bath and refluxed for 7 hours. Upon completion of the reaction, it was cooled to room temperature and allowed to stand overnight. Subsequently, 150 ml of dichloromethane was added to the reaction mixture and the insoluble material was removed by filtration. The filtrate was washed twice with 50 ml of water and then dried with 30 g of anhydrous sodium sulfate. After evaporation of the solvent, the crude product was obtained. The crude product was purified by column chromatography (using 150 g of Fuji Silicia's NH silica gel as the carrier and cyclohexane as the eluent) to give 4.4 g of N,N'-diphenyl-N,N'-bis(3-methylphenyl)-1,1'-biphenyl-4,4'-diamine (TPD) in a final yield of 85.2%.

References

[1] Tetrahedron Letters, 1998, vol. 39, # 16, p. 2367 - 2370
[2] Journal of the Chinese Chemical Society, 2001, vol. 48, # 6 A, p. 1059 - 1064
[3] Patent: EP2157077, 2010, A1. Location in patent: Page/Page column 9-10
[4] Journal of the American Chemical Society, 2012, vol. 134, # 50, p. 20262 - 20265
[5] Patent: JP5777106, 2015, B2. Location in patent: Paragraph 0037

N,N'-Bis(3-methylphenyl)-N,N'-bis(phenyl)benzidine(65181-78-4)Related Product Information

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