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
• Article Data: 13

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

General Description

2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine is a chemical compound with the molecular formula C24H25ClN3. It is a triazine derivative that is commonly used as a UV stabilizer and light stabilizer in various products, such as plastics, coatings, adhesives, and rubber. Its structure consists of a triazine ring with two tert-butylphenyl groups and a chlorine atom attached. 2,4-bis(4-(tert-butyl)phenyl)-6-chloro-1,3,5-triazine is known for its ability to absorb and dissipate UV radiation, which helps to prevent degradation and discoloration in the materials it is added to. It is also used as an antioxidant and has been shown to have low toxicity in studies.

Upstream product

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

Triazine compound and preparation method thereof

The invention belongs to the technical field of organic chemical synthesis, and particularly relates to a triazine compound and a preparation method thereof. Most of existing triazine compounds and derivatives thereof are prepared through ring closing or an aromatic halogenated compound Grignard method, the reaction process is complex, and manpower and material resources are wasted. The invention provides the triazine compound. The general formula of the compound is shown in the specification, or reaction raw materials are cheap and easy to obtain, the reaction operation is simple, side reactions are few, and the yield is high.

NOVEL TRIAZINE COMPOUND, COMPOSITION THEREOF AND PREPARATION METHOD THEREOF

The present invention relates to novel triazine compounds, a process for their production and compositions comprising the compounds. Triazine compounds can be applied to a variety of organic materials to prevent UV damage, such as polyols, plastics, adhes