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3,4,4'-TRIAMINODIPHENYL ETHER, with the molecular formula C12H13N3O, is a white crystalline solid that is insoluble in water but soluble in organic solvents. It is a chemical compound known for its strong aromatic odor and is commonly used as a curing agent for epoxy resins. 3,4,4'-TRIAMINODIPHENYL ETHER is also recognized for its excellent thermal and chemical resistance, making it suitable for various applications across different industries.

6264-66-0

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6264-66-0 Usage

Uses

Used in Composites and Adhesives Industry:
3,4,4'-TRIAMINODIPHENYL ETHER is used as a curing agent for epoxy resins, which are essential in the production of composites and adhesives. Its role in this application is to harden the epoxy, providing enhanced strength and durability to the final product.
Used in Coatings Industry:
In the coatings industry, 3,4,4'-TRIAMINODIPHENYL ETHER serves as a curing agent for epoxy resins, contributing to the formation of high-quality coatings with improved adhesion, hardness, and resistance to environmental factors.
Used in Aerospace Industry:
3,4,4'-TRIAMINODIPHENYL ETHER is utilized in the aerospace industry due to its excellent thermal and chemical resistance. Its properties make it ideal for use in the production of components and materials that require high-performance characteristics in extreme conditions.
Used in Automotive Industry:
The automotive industry also benefits from the use of 3,4,4'-TRIAMINODIPHENYL ETHER, particularly in the manufacturing of components and materials that demand high durability and resistance to various environmental factors, such as temperature fluctuations and chemical exposure.
Used in Electronics Industry:
In the electronics industry, 3,4,4'-TRIAMINODIPHENYL ETHER is employed for its thermal and chemical resistance properties, making it suitable for use in the production of materials and components that require protection from heat and chemical exposure, ensuring the longevity and reliability of electronic devices.
Used as an Intermediate in Chemical Synthesis:
3,4,4'-TRIAMINODIPHENYL ETHER is also used as an intermediate in the synthesis of various dyes and pharmaceuticals, highlighting its versatility and importance in the chemical industry.
Safety Precautions:

Check Digit Verification of cas no

The CAS Registry Mumber 6264-66-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6264-66:
(6*6)+(5*2)+(4*6)+(3*4)+(2*6)+(1*6)=100
100 % 10 = 0
So 6264-66-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N3O/c13-8-1-3-9(4-2-8)16-10-5-6-11(14)12(15)7-10/h1-7H,13-15H2

6264-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-aminophenoxy)benzene-1,2-diamine

1.2 Other means of identification

Product number -
Other names 3,4,4'-Triaminodiphenyl oxide

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:6264-66-0 SDS

6264-66-0Relevant articles and documents

Chemical compounds

-

, (2008/06/13)

Benzimidazole derivatives, which are useful as TIE-2 and/or VEGFR2 inhibitors are described herein. The described invention also includes methods of making such benzimidazole derivatives as well as methods of using the same in the treatment of hyperproliferative diseases.

Synthesis of 3,4,4′- and 2′,3,4-triaminodiphenyl ethers

Pilyugin,Mikhailyuk,Kiseleva,Kuznetsova,Chikisheva,Kosareva

, p. 1105 - 1109 (2007/10/03)

Procedures were developed for preparing 3,4,4′- and 2′,3,4-triaminodiphenyl ethers by the reaction of 4-acetylaminophenol with, respectively, 4-nitro- or 2-nitrochlorobenzene, followed by nitration of the resulting 4-acetylamino-4′- or -2′-nitrodiphenyl ether, hydrolysis of the product, 4-acetylamino-3,4′- or -2′,3- dinitrodiphenyl ether, and reduction of 4-amino-3,4′- or -2′-3-dinitrodiphenyl ether.

Synthesis of methyl 5(6)-(4-aminophenoxy)-and 5(6)-(2-aminophenoxy)-2- benzimidazolyl carbamates and their biological properties

Pilyugin,Mikhailyuk,Kosareva,Chikisheva,Kiseleva,Kuznetsova,Vorobyeva,Klimakova

, p. 1154 - 1160 (2007/10/03)

A procedure was developed for preparation of methyl 5(6)-(4-aminophenoxy)- and 5(6)-(2-aminophenoxy)-2-benzimidazolyl carbamates by reaction of 3,4,4′-triaminodiphenyl or 3,4,2′-triaminodiphenyl ethers respectively with methyl cyanocarbamate in water solution in the presence of 7-10 molar excess of acetic acid. The helminthicidal properties, embryotoxicity, and overall toxicity of compounds obtained were estimated.

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