Skip to Content
Merck
All Photos(1)

Documents

773824

Sigma-Aldrich

2,9-Diheptylanthra[2,1,9-def:6,5,10-def′]diisoquinoline-1,3,8,10(2H,9H)tetrone

99%

Synonym(s):

N,N′-Diheptyl-3,4,9,10-perylenedicarboximide, HepPTC, PDI-C7

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C38H38N2O4
CAS Number:
Molecular Weight:
586.72
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

Assay

99%

form

powder

mp

207-214 °C

λmax

254 nm in dichloromethane

semiconductor properties

N-type (mobility=1.4x10−2 cm2/V·s)

SMILES string

CCCCCCCN1C(=O)c2ccc3c4ccc5C(=O)N(CCCCCCC)C(=O)c6ccc(c7ccc(C1=O)c2c37)c4c56

InChI

1S/C38H38N2O4/c1-3-5-7-9-11-21-39-35(41)27-17-13-23-25-15-19-29-34-30(38(44)40(37(29)43)22-12-10-8-6-4-2)20-16-26(32(25)34)24-14-18-28(36(39)42)33(27)31(23)24/h13-20H,3-12,21-22H2,1-2H3

InChI key

WXLGICNTPAGZCR-UHFFFAOYSA-N

Application

High electron transporting character; Perylenebis(dicarboximide)s (PDIs) can be used as n-type materials for organic fieldeffect transistors (OFETs);
Good optical properties; it can also be used for solution-processed organic phototransistors (OPTs);
Excellent candidates as electron accepting building blocks for organic photovoltaics (OPVs).

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Dual carrier traps related hysteresis in organic inverters with polyimide-modified gate-dielectrics
Applied Physics Letters, 96, 153302/1-153302/3 (2010)
Geometry and Electronic Coupling in Perylenediimide Stacks: Mapping Structure-Charge Transport Relationships
Journal of the American Chemical Society, 132, 1739-1739 (2010)

Articles

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

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

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.

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.

See All

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