25811-56-7

Basic information

• Product Name: PDI-C6
• Synonyms: 2,9-Dihexylanthra[2,1,9-def:6,5,10-d′e′f′]diisoquinoline-1,3,8,10(2H,9H)tetrone;N,N′-Dihexyl-3,4,9,10-perylenedicarboximide;PDI-C6;2,9-Dihexylanthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)tetrone 98%
• CAS NO: 25811-56-7
• Molecular Formula: C36H34N2O4
• Molecular Weight: 558.67
• Mol File: 25811-56-7.mol
• Article Data: 5

Chemical Properties

• Melting Point: 196-200°C
• Appearance: /
• CAS DataBase Reference: PDI-C6(CAS DataBase Reference)
• NIST Chemistry Reference: PDI-C6(25811-56-7)
• EPA Substance Registry System: PDI-C6(25811-56-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 25811-56-7(Hazardous Substances Data)

Usage

Description

PDI-C6, a type of Perylenebis(dicarboximide), is an organic compound known for its high electron transporting character, good optical properties, and suitability for use in various electronic applications. It is a promising material for the development of advanced electronic devices and systems.

Uses

Used in Electronics Industry:
PDI-C6 is used as an n-type material for organic field-effect transistors (OFETs) due to its high electron transporting character. This makes it a valuable component in the development of flexible and low-cost electronic devices.
Used in Optoelectronics Industry:
PDI-C6 is used as a component in solution-processed organic phototransistors (OPTs) because of its good optical properties. This application allows for the creation of high-performance optoelectronic devices that can be manufactured using solution-based processes.
Used in Solar Energy Industry:
PDI-C6 is an excellent candidate as an electron accepting building block for organic photovoltaics (OPVs). Its properties make it a valuable component in the development of efficient and cost-effective solar cells that can convert sunlight into electricity.

Upstream product

• 111-26-2 hexan-1-amine 
• 128-69-8 perylene-3,4,9,10-tetracarboxylic acid 3,4:9,10-dianhydride 
• 6033-61-0 hexanal oxime 

Relevant articles and documents

Organic field-effect transistors based on disubstituted perylene diimides: Effect of alkyl chains on the device performance

The preparation and systematic investigation of n-type semiconductor materials based on disubstituted perylene diimides (PDIs) possessing alkyl chains with variable length (from C4 to C12) are reported. It was shown that electrical characteristics of field-effect transistors can be tuned by changing the length of the alkyl chains in the PDIs used as semiconductor materials.

Green and highly efficient synthesis of perylene and naphthalene bisimides in nothing but water

High-purity, symmetrically substituted perylene and naphthalene bisimides were obtained by hydrothermal condensation of monoamines with the corresponding bisanhydride. The hydrothermal imidization proceeds quantitatively, without the need for organic solvents, catalysts or excess of the amines.

Synthesis and Reactions of Perylenecarboxylic Acid Derivatives. VIII. Synthesis of N-Alkyl-3,4:9,10-Perylenetetracarboxylic Monoanhydride Monoimide

The condensations of 3,4:9,10-perylenetetracarboxylic dianhydride with alkylamines (isobutyl-, pentyl-, hexyl-, and octylamines) were spectroscopically determined.Under all of the reaction conditions employed, N-alkyl-3,4:9,10-perylenetetracarboxylic monoanhydride monoimide (2a-d) (alkyl=a; isobutyl, b; pentyl, c; hexyl, d; octyl) were obtained.As the reaction proceeded, the yield of 2a-d increased at an initial stage but decreased gradually after reaching a maximum.This maximum yield of 2a-d was: 2a; 85-88percent, 2b; 85-89percent, 2c; 78-84percent, 2d; 79-85percent.The kinetics of the reaction were also examined.