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767905

4,4′-Dimethoxydiphenylamine

Name: 4,4′-Dimethoxydiphenylamine
Brand: ALDRICH

99%

Synonym(s):

4-Biphenylamine,4,4′-dimethoxy-, 4-Methoxy-N-(4-methoxyphenyl)aniline, p,p′-Dimethoxydiphenylamine, Benzenamine,4-methoxy-N-(4-methoxypheny)-, Bis(4-methoxyphenyl)-amine, Bis(4-methoxyphenyl)amine, Bis(p-anisyl)amine, Bis(p-methoxyphenyl)amine, Di-p-anisylamine, Di-p-methoxyphenylamine, Termofleks A

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About This Item

Empirical Formula (Hill Notation):

C₁₄H₁₅NO₂

CAS Number:

101-70-2

Molecular Weight:

229.27

NACRES:

NA.23

PubChem Substance ID:

329767347

UNSPSC Code:

12352103

EC Number:

202-968-1

MDL number:

MFCD00014895

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Properties

Quality Level

100

assay

99%

form

powder

mp

100-104 °C

SMILES string

COc1ccc(Nc2ccc(OC)cc2)cc1

InChI

1S/C14H15NO2/c1-16-13-7-3-11(4-8-13)15-12-5-9-14(17-2)10-6-12/h3-10,15H,1-2H3

InChI key

VCOONNWIINSFBA-UHFFFAOYSA-N

Description

General description

4,4′-Dimethoxydiphenylamine is an aromatic amine that is used as a hole transporting material that facilitates efficiency mobility of charges in an electrochemical device.

Application

It can be used as a hole transporting material in the synthesis of 4,4′-dimethoxydiphenylamine-substituted 9,9′- bifluorenylidene with a power efficiency of ~18% which may be used in combination with an electron transporting layer in the fabrication of polymeric solar cells. It may also be used in the preparation of dimethyldiphenylamino functionalized carbazoles as electronically active materials which can potentially be used in the development of optoelectronic devices.

pictograms

GHS08,GHS07

signalword

Warning

hcodes

H315,H319,H335,H351

pcodes

P201 - P302 + P352 - P305 + P351 + P338 - P308 + P313

Hazard Classifications

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Articles

Progress for High Performance Tandem Organic Solar Cells

Professor Chen (Nankai University, China) and his team explain the strategies behind their recent record-breaking organic solar cells, reaching a power conversion efficiency of 17.3%.

Thermally stable triaryl amino chromophores with high molecular hyperpolarizabilities

Spraul, Bryan K., et al.

Tetrahedron Letters, 45(16), 3253-3256 (2004)

Diphenylamino-substituted derivatives of 9-phenylcarbazole as glass-forming hole-transporting materials for solid state dye sensitized solar cells.

Tomkeviciene A, et al.

Synthetic Metals, 162(23), 1997-2004 (2012)

Triarylene linked spacer effect for dye-sensitized solar cells

Chang, Y. J., Wu, Y. J., Chou, P. T., Watanabe, M., & Chow, T. J.

Thin Solid Films, 558, 330-336 (2014)

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Global Trade Item Number

SKU	GTIN
767905-1G	04061832924397
767905-5G	04061832924403