Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

264229

Sigma-Aldrich

N,N′-Bis(2,5-di-tert-butylphenyl)-3,4,9,10-perylenedicarboximide

Dye content 97 %

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C52H50N2O4
CAS Number:
Molecular Weight:
766.96
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

assay

97%

form

solid

composition

Dye content, 97%

mp

>300 °C (lit.)

λmax

528 nm

semiconductor properties

N-type (mobility=1.8x10−4 cm2/V·s)

SMILES string

CC(C)(C)c1ccc(c(c1)N2C(=O)c3ccc4c5ccc6C(=O)N(C(=O)c7ccc(c8ccc(C2=O)c3c48)c5c67)c9cc(ccc9C(C)(C)C)C(C)(C)C)C(C)(C)C

InChI

1S/C52H50N2O4/c1-49(2,3)27-13-23-37(51(7,8)9)39(25-27)53-45(55)33-19-15-29-31-17-21-35-44-36(22-18-32(42(31)44)30-16-20-34(46(53)56)43(33)41(29)30)48(58)54(47(35)57)40-26-28(50(4,5)6)14-24-38(40)52(10,11)12/h13-26H,1-12H3

InChI key

BIYPCKKQAHLMHG-UHFFFAOYSA-N

General description

N,N′-Bis(2,5-di-tert-butylphenyl)-3,4,9,10-perylenedicarboximide (BTBP) is a fluorescence dye that can be used as an electron acceptor. It has an extinction coefficient of 7.4 x 104 cm-1 mol-1 dm3.

Application

An n-channel organic semiconductor.
BTBP is a dye that can be used in the development of organic electronic based devices which include organic light emitting diodes(OLED), electroluminescent device and organic solar cells(OSCs).

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Three-layered multicolor organic electroluminescent device.
Yoshida M, et al.
Applied Physics Letters, 69(6), 734-736 (1996)
The cybotactic region surrounding fluorescent probes dissolved in 1-butyl-3-methylimidazolium hexafluorophosphate: effects of temperature and added carbon dioxide.
Baker SN, et al.
The Journal of Physical Chemistry B, 105(39), 9663-9668 (2001)
Effects of doping dyes on the electroluminescent characteristics of multilayer organic light-emitting diodes.
Suzuki H and Hoshino S
Journal of Applied Physics, 79(11), 8816-8822 (1996)
Insulated molecular wire with highly conductive pi-conjugated polymer core.
Terao J, et al.
Journal of the American Chemical Society, 131(50), 18046-18047 (2009)
Self-assembled gelators for organic electronics.
Babu SS, et al.
Angewandte Chemie (International Edition in English), 51(8), 1766-1776 (2012)

Articles

Fabrication procedure of organic field effect transistor device using a soluble pentacene precursor.

Intrinsically stretchable active layers for organic field-effect transistors (OFET) are discussed. Polymer structural modification & post-polymerization modifications are 2 methods to achieve this.

Solution-processed organic photovoltaic devices (OPVs) have emerged as a promising clean energy generating technology due to their ease of fabrication, potential to enable low-cost manufacturing via printing or coating techniques, and ability to be incorporated onto light weight, flexible substrates.

There is widespread demand for thin, lightweight, and flexible electronic devices such as displays, sensors, actuators, and radio-frequency identification tags (RFIDs). Flexibility is necessary for scalability, portability, and mechanical robustness.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service