4021-36-7

Usage

Uses

Used in Plastics Industry:
2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine is used as a UV stabilizer and antioxidant for plastics, ensuring their resistance to UV-induced degradation and improving their overall performance and longevity.
Used in Rubber Industry:
In the rubber industry, 2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine serves as a stabilizer, protecting rubber materials from the damaging effects of UV radiation and prolonging their service life.
Used in Adhesives Production:
2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine is used as a stabilizer in the production of adhesives to enhance their durability and resistance to UV degradation, ensuring stronger and longer-lasting bonds.
Used in Coatings Production:
As a stabilizer in coatings, 2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine helps to maintain the integrity and appearance of coated surfaces by protecting them from UV-induced damage.
Used in Film Production:
2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine is used in the production of films to provide UV stabilization, ensuring the films remain clear and undamaged over time.
Used in Packaging Materials:
In the packaging industry, 2,4,6-tris(4-tert-butylphenoxy)-1,3,5-triazine is utilized as a stabilizer to protect packaging materials from UV degradation, thus preserving the quality and appearance of the packaged products.

Upstream product

• 1132-16-7 1-tert-butyl-4-cyanato-benzene 
• 98-54-4 para-tert-butylphenol 
• 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 academic research and scientific papers

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.

Attempt to Synthesize Hindered 2,4,6-Tri-Aryloxy-s-Triazines: Bis(2,4-di-tert-Butylphenyl) Carbonate – Crystal Structure

Some less hindered 2,4,6-tri-aryloxy-s-triazines were synthesized through the reaction of the corresponding phenols as a starting materials with cyanogen bromide (BrCN) to obtain the corresponding arylcyanates and then trimerized. Unexpectedly, 2,4-di-tert-butyl-1-cyanatobenzene derived from 2,4-di-tert-butylphenol did not trimerize but, indeed, yielded bis(2,4-di-tert-butylphenyl) carbonate. The structures of 2,4,6-tri-aryloxy-s-triazines and bis(2,4-di-tert-butylphenyl) carbonate were characterized by means of IR, 1H, and 13C NMR spectroscopies. Also the structure of the latter compound was studied by X-ray crystallography.

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.

SYNTHESIS OF TRIARYL CYANURATES CATALYSED BY POLYETHYLENE GLYCOL IN A TWO-PHASE SYSTEM : PHASE TRANSFER CATALYSIS

The synthesis of triaryl cyanurates (2,4,6-triaryloxy-1,3,5-triazines) was accomplished at room temperature in high yields in a two-phase system using PEG-400 as a phase transfer catalyst.