253158-13-3

Basic information

• Product Name: 2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine
• Synonyms: 2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine;2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine
• CAS NO: 253158-13-3
• Molecular Formula: C23H26ClN3
• Molecular Weight: 379.92564
• EINECS: -0
• Mol File: 253158-13-3.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine(253158-13-3)
• EPA Substance Registry System: 2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine(253158-13-3)

Safety Data

• Hazardous Substances Data: 253158-13-3(Hazardous Substances Data)

Usage

Uses

Used in Plastics Industry:
2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine is used as a UV stabilizer and light stabilizer for plastics to protect them from degradation and discoloration caused by exposure to sunlight and other UV sources.
Used in Coatings Industry:
In the coatings industry, 2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine is used as a stabilizer to enhance the durability and color retention of coatings applied to various surfaces.
Used in Adhesives Industry:
2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine is used as a stabilizer in adhesives to improve their resistance to UV radiation, thereby extending their service life and maintaining their bonding strength.
Used in Rubber Industry:
In the rubber industry, 2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine is used as a UV stabilizer and light stabilizer to prevent the rubber from degrading and discoloring when exposed to sunlight and other UV sources.
Used as an Antioxidant:
2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine is also used as an antioxidant in various applications, helping to prevent oxidation and degradation of materials, thereby extending their lifespan and maintaining their properties.
Low Toxicity:
Studies have shown that 2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine has low toxicity, making it a safer option for use in various industries where exposure to humans or the environment is a concern.

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 22385-77-9 1-bromo-3,5-di-tert-butylbenzene 
• 63488-10-8 4-tert-butylmagnesium bromide 
• 123324-71-0 p-tert-butylphenylboronic acid 
• 4210-32-6 4-tert-butyl benzonitrile 
• 52866-85-0 4-tert-butylphenyllithium 
• 253185-03-4 tert-butylbenzene 

Downstream Products

• 927898-18-8 2-(4-bromophenyl)-4,6-bis(4-tert-butylphenyl)-[1,3,5]-triazine 

Relevant articles and documents

Rational molecular design of deep blue thermally activated delayed fluorescent emitters for high efficiency fluorescent and hyperfluorescent devices

Two deep blue thermally activated delayed fluorescent (TADF) emitters with peripheral alkyl branches surrounding the donor and acceptor moieties were synthesized to explore ideal design of deep blue TADF emitters for fluorescence and hyperfluorescence in terms of quantum efficiency. The TADF emitters having the multiple alkyl branches protecting the donor and acceptor moieties performed better than the emitter without the alkyl branch or with the alkyl branch only in the donor or acceptor unit. The TADF emitters with the peripheral alkyl branches both in the donor and acceptor units showed a high quantum efficiency above 22.0%, a deep blue color coordinate of (0.15, 0.20), and doping concentration independent emission color as TADF emitters, and 13.7% quantum efficiency in the TADF sensitized hyperfluorescent device. Therefore, the multiple alkyl modification method of both donor and acceptor units of TADF emitters can resolve the issues of TADF emitters for ideal device performances.

A t-butyl modification approach of acceptor moiety for stable deep blue emission in thermally activated delayed fluorescent devices

A t-butyl modification method of an acceptor moiety was developed as a molecular design approach of blue emitters to shift the emission color to deep blue region and to stabilize the emission color according to doping concentration. A phenyl unit of triphenyltriazine acceptor moiety of blue thermally activated delayed fluorescent emitter was modified with either one or two t-butyl units to study the effect of the t-butyl unit on the electroluminescence emission of the blue thermally activated delayed fluorescent emitters. It was found that two t-butyl units introduced in the phenyl unit of the triphenyltriazine shifted the emission color to deep blue emission while keeping the deep blue color over wide doping concentration range.

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