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Merck
CN

793256

Bisbenzimidazo[2,1-a:2′,1′-a′]anthra[2,1,9-def:6,5,10-d′e′f′]diisoquinoline-10,21-dione

97%

Synonym(s):

Bisbenzimidazo[2,1-a:2′,1′-a′]anthra[2,1,9-def:6,5,10-d′e′f′]diisoquinoline-10,21-dione, N,N′-Diphenylglyoxaline-3,4,9,10-perylenetetracarboxylic acid diacidamide, PTCBI

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About This Item

Empirical Formula (Hill Notation):
C36H16N4O2
CAS Number:
55034-79-2
Molecular Weight:
536.54
UNSPSC Code:
12352103
PubChem Substance ID:
329768408
MDL number:
MFCD00167037

Key Documents

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InChI

1S/C36H16N4O2/c41-35-23-15-11-19-18-10-14-22-32-24(36(42)40-28-8-4-2-6-26(28)38-34(22)40)16-12-20(30(18)32)17-9-13-21(31(23)29(17)19)33-37-25-5-1-3-7-27(25)39(33)35/h1-16H

SMILES string

O=C1C2=C3C(C4=NC5=CC=CC=C5N41)=CC=C(C6=CC=C(C(N7C8=NC9=C7C=CC=C9)=O)C%10=C8C=CC%11=C6%10)C3=C%11C=C2

InChI key

CNXXSKARMYGQBG-UHFFFAOYSA-N

assay

97%

form

solid

mp

>300 °C

Quality Level

100

Application

Excellent materials as electron accepting building blocks for organic photovoltaics (OPVs); organic field effect transistors (OFETs); organic photoconductive sensors and organic electroluminescent cells.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKBT8286V

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Peter Peumans et al.
Nature, 425(6954), 158-162 (2003-09-12)
The power conversion efficiency of small-molecular-weight and polymer organic photovoltaic cells has increased steadily over the past decade. This progress is chiefly attributable to the introduction of the donor-acceptor heterojunction that functions as a dissociation site for the strongly bound
Influence of Dielectric Surface Chemistry on the Microstructure and Carrier Mobility of an n-Type Organic Semiconductor
Dhagat et al.
Advances in Functional Materials, 19(15), 2365-2372 (2009)

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