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1,6,7,12-Tetra-tert-butylphenoxyperylene-3,4,9,10-tetracarboxylic dianhydride is an organic compound with a complex chemical structure, belonging to the perylene tetracarboxylic dianhydride family. 1,6,7,12-Tetra-tert-butylphenoxyperylene-3,4,9,10-tetracarboxylic dianhydride is distinguished by the presence of tert-butyl groups and a phenoxy group, which contribute to its enhanced solubility and thermal stability. It is characterized by its vibrant red color and high thermal resistance, making it suitable for a range of applications.

545387-15-3

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545387-15-3 Usage

Uses

Used in Paints and Plastics Industry:
1,6,7,12-Tetra-tert-butylphenoxyperylene-3,4,9,10-tetracarboxylic dianhydride is used as a pigment for its vibrant red color and high thermal resistance, making it ideal for paints and plastics that require coloration and stability under high-temperature conditions.
Used in Organic Electronics:
1,6,7,12-Tetra-tert-butylphenoxyperylene-3,4,9,10-tetracarboxylic dianhydride is utilized as an electron transport material in organic electronics due to its good electron transport properties, which are essential for the performance of these devices.
Used in Optoelectronic Devices:
In the optoelectronics industry, 1,6,7,12-Tetra-tert-butylphenoxyperylene-3,4,9,10-tetracarboxylic dianhydride is employed for its electron transport capabilities, which are crucial for the efficient functioning of various optoelectronic devices, such as solar cells and light-emitting diodes.

Check Digit Verification of cas no

The CAS Registry Mumber 545387-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,5,3,8 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 545387-15:
(8*5)+(7*4)+(6*5)+(5*3)+(4*8)+(3*7)+(2*1)+(1*5)=173
173 % 10 = 3
So 545387-15-3 is a valid CAS Registry Number.

545387-15-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6,12,13-tetrakis(4-(tert-butyl)phenoxy)-2,9-dioctadecylanthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetraone

1.2 Other means of identification

Product number -
Other names 1,6,7,12-TETRA-TERT-BUTYLPHENOXY-N,N'-BIS(OCTADECYL)PERYLENE-3,4,9,10-TETRACARBOXYLIC ACID DIIMIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:545387-15-3 SDS

545387-15-3Downstream Products

545387-15-3Relevant academic research and scientific papers

Synthesis, electrochemical and optical absorption properties of new perylene-3,4:9,10-bis(dicarboximide) and perylene-3,4:9,10-bis(benzimidazole) derivatives

Perrin, Lara,Hudhomme, Pietrick

experimental part, p. 5427 - 5440 (2011/11/29)

A series of perylene-3,4:9,10-bis(dicarboximide) (PBI) and perylene-3,4:9,10-bis(benzimidazole) (PTCBI) derivatives that are di-or tetra-substituted at the bay region by electron-donating or electron-withdrawing groups have been synthesized as soluble n-type semiconductors. Optical absorption spectroscopy and electrochemical analysis show that the nature of substitution at the bay region plays a crucial role in the modulation of the electronic properties of these PBI and PTCBI derivatives. Examination of these optical and electrochemical data in the light of energy levels identified by theoretical studies allowed a relationship between the structure and the electronic properties to be established. A relationship between the structure and electronic properties of n-type semiconductors from perylene-3,4:9,10- bis(dicarboximide) (PBI) and perylene-3,4:9,10-bis(benzimidazole) (PTCBI) series substituted at the bay region by electron-donating or electron-withdrawing groups has been established by using the complementary techniques of absorption spectroscopy, electrochemical analysis and theoretical calculations. Copyright

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