112100-07-9

Basic information

• Product Name: Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone
• Synonyms: 1,6,7,12-Tetraphenoxyperylene-N,N'-bis(2,6-diisopropylphenyl)-3,4:9,10-tetracarboxdiimide;N, N'-Bis(2,6-diisopropylphenyl)-1,6,7,12-tetrephenoxyperylene-3,4,9,10-tetracarboxdiimide;Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone,2,9-bis[2,6-bis(1-methylethyl)phenyl]-5,6,12,13-tetraphenoxy-;Red fluorescence dye R-300
• CAS NO: 112100-07-9
• Molecular Formula: C72H58 N2 O8
• Mol File: 112100-07-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone(CAS DataBase Reference)
• NIST Chemistry Reference: Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone(112100-07-9)
• EPA Substance Registry System: Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone(112100-07-9)

Safety Data

• Hazardous Substances Data: 112100-07-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Used in Organic Electronics:
In the field of organic electronics, Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone is utilized for its electronic properties, such as charge transport and light absorption, which are crucial for the development of organic semiconductors and other electronic devices.
Used in Materials Science:
Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone is employed in materials science for its potential to contribute to the creation of new materials with enhanced properties. Its unique structure may lead to the development of advanced composites, coatings, or other materials with specific applications in various industries.

Upstream product

• 24544-04-5 2,6-diisopropylbenzenamine 
• 156028-26-1 1,6,7,12-tetrachloro-perylene-3,4,9,10-tetracarboxylic acid dianhydride 
• 118129-60-5 1,7-dibromoperylene-3,4,9,10-tetracarboxylic dianhydride 
• 81-33-4 3,4,9,10-perylene tetracarboxyxlic acid diimide 

Downstream Products

• 937040-91-0 N-(2,6-diisopropylphenyl)-1,6,7,12-tetraphenoxyperylene-3,4:9,10-tetracarboxy-9,10-monoanhydride-3,4-monoimide 
• 156028-31-8 1,6,7,12-tetra(4-phenoxy)perylene-3,4:9,10-tetracarboxylic acid dianhydride 

Relevant articles and documents

PERYLENE BISIMIDE BASED COMPOUNDS AND DYES COMPRISING THE SAME

The present invention relates to a perylene bisimide-based compound represented by the following chemical formula 1 capable of providing dye having less fluorescence reduction at a high temperature while having excellent solubility in an organic solvent,

The synthesis and characterisation of the perylene acid dye inks for digital textile printing

Five perylene acid dyes were synthesized to manufacture water-based inks for the high-speed ink jet printing process, including digital textile printing. All the synthesized perylene dyes exhibited superior stability and optical properties compared to a commercially used azo dye. Their water solubility was efficiently enhanced by introducing bulky and hydrophilic substituents to ensure excellent long-term stability when formulated as water-based inks. The water-based inks with these perylene dyes showed outstanding print clarity with the colours different from the basic colour composition of the existing digital textile printing inks. They also exhibited good ejection performance and helped conduct well-controlled pattern printing when used in a commercial ink jet printing machine.

Preparation method of Lumogen Red F300

The invention relates to Lumogen Red F300, in particular to a preparation method of the Lumogen Red F300. The preparation method comprises the following steps that 1,6,7,12-tetrabromo-3,4,9,10-perylenetetracarboxylic dianhydride is prepared; a 1,6,7,12-tetraphenoxy-3,4,9,10-perylenetetracarboxylic potassium aqueous solution is prepared; and an amination reaction is performed. The preparation method is more scientific and reasonable; and the color fastness is relatively higher, so that the Lumogen Red F300 is close to functional dye.

Kinetically Trapped Supramolecular Assembly of Perylene Dianhydride Derivative in Methanol: Optical Spectra, Morphology, and Mechanisms

Supramolecular self-assembly has attracted increasing attention as a breakthrough methodology in the fields of nanoscience and nanotechnology. Herein, a perylene dianhydride derivative (TP-PDA) self-assembles into well-defined nanospheres through a nuclea