4021-36-7

Basic information

• Product Name: 2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine
• CAS NO: 4021-36-7
• Molecular Formula: C₃₃H₃₉N₃O₃
• Molecular Weight: 525.6811
• Mol File: 4021-36-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 625.6°C at 760 mmHg
• Flash Point: 215.4°C
• Density: 1.093g/cm³
• Vapor Pressure: 6.81E-15mmHg at 25°C
• Refractive Index: 1.557
• CAS DataBase Reference: 2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine(4021-36-7)
• EPA Substance Registry System: 2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine(4021-36-7)

Safety Data

• Hazardous Substances Data: 4021-36-7(Hazardous Substances Data)

Usage

General Description

2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine is a chemical compound that belongs to the class of triazine derivatives. It is commonly used as a UV stabilizer and antioxidant in the production of various materials such as plastics, rubber, and adhesives. 2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine helps to prevent degradation caused by exposure to ultraviolet radiation and helps to extend the lifespan of the materials it is added to. Additionally, it can also be used as a stabilizer in the production of various products, such as coatings, films, and packaging materials. Due to its properties, 2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine is an important chemical in the manufacturing industry and is widely used to improve the durability and performance of a wide range of products.

Upstream product

• 98-54-4 para-tert-butylphenol 
• 1132-16-7 1-tert-butyl-4-cyanato-benzene 
• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 5787-50-8 sodium 4-tert-butylphenolate 

Downstream Products

• 103826-50-2 1-(1,1-dimethylethyl)-4-(2-phenylethenyl)benzene 
• 253185-03-4 tert-butylbenzene 

Relevant articles and documents

Nickel-catalysed C–O bond reduction of 2,4,6-triaryloxy-1,3,5-triazines in 2-methyltetrahydrofuran

A nickel-catalysed reduction of phenol derivatives activated by 2,4,6-trichloro-1,3,5-triazine (TCT) in ecofriendly 2-methyltetrahydrofuran (2-MeTHF) is described. The phenol-TCT derivatives were readily prepared using grinding method in short time without further purification. This catalytic system allowed the facile C–O cleavage of phenol-TCT derivatives under mild reaction conditions with high efficiency and good functional group tolerance. Gram-scale reaction was also achieved. Particularly, sequential functionalization of phenol-TCT derivatives followed by C–O bond reduction could also be realized, affording the high value-added products in moderate to good yields.

Efficient Ni-catalyzed conversion of phenols protected with 2,4,6-trichloro-1,3,5-triazine (TCT) to olefins

An efficient Ni(COD)2/dppf catalyzed olefination of Ar-O-TCT as synthetic equivalents of aryl halides is described. Activation of C-O bonds in phenols as readily available compounds was achieved with 2,4,6-trichloro-1,3,5-triazine (TCT). This method provides practical access to 1,2-disubstituted olefins in high yields and high functional group compatibility.