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Usage

Uses

Used in Coatings Industry:
Trimethallyl isocyanurate is used as a crosslinking agent for improving the durability and performance of coatings. Its addition results in coatings with enhanced resistance to heat, chemicals, and mechanical stress, making them suitable for various applications, including automotive and industrial coatings.
Used in Adhesives Industry:
In the adhesives industry, trimethallyl isocyanurate is utilized as a crosslinking agent to create strong bonds between different materials. Its ability to improve the adhesive's thermal and chemical stability makes it ideal for use in high-performance adhesives for various applications, such as in the assembly of automotive components and construction materials.
Used in Thermosetting Resins Industry:
Trimethallyl isocyanurate is employed as a crosslinking agent in the production of thermosetting resins. Its incorporation leads to resins with superior mechanical properties and resistance to heat and chemicals, which are essential for applications in the aerospace and construction industries.
Used in Automotive Industry:
Trimethallyl isocyanurate is used as a crosslinking agent in the automotive industry to enhance the performance of materials used in the manufacturing of vehicles. Its contribution to improved mechanical properties and resistance to heat and chemicals ensures the longevity and reliability of automotive components.
Used in Aerospace Industry:
In the aerospace industry, trimethallyl isocyanurate is utilized as a crosslinking agent to improve the performance of materials used in aircraft construction. Its ability to enhance thermal and chemical resistance, as well as mechanical properties, is crucial for the development of lightweight and durable aerospace components.
Used in Construction Industry:
Trimethallyl isocyanurate is employed as a crosslinking agent in the construction industry to improve the performance of building materials. Its contribution to enhanced thermal and chemical resistance, as well as mechanical properties, ensures the durability and stability of construction materials in various applications.
It is important to handle trimethallyl isocyanurate with care, as it may cause irritation or allergic reactions upon contact with skin or inhalation. Proper safety measures should be taken during its use to minimize potential health risks.

InChI:InChI=1/C15H21N3O3/c1-10(2)7-16-13(19)17(8-11(3)4)15(21)18(14(16)20)9-12(5)6/h1,3,5,7-9H2,2,4,6H3

Upstream product

• 1458-98-6 2-methyl-3-bromo-1-propene 
• 3047-33-4 sodium cyanurate 
• 16715-84-7 2,4,6-tris(methallyloxy)-1,3,5-triazine 
• 101-37-1 triallyl cyanurate 
• 108-80-5 cyanuric acid 
• 563-47-3 3-Chloro-2-methylpropene 

Relevant academic research and scientific papers

Photosensitive resin composition for color filter and uses thereof

The present invention relates to a photosensitive resin composition for a color filter and uses thereof. The photosensitive resin composition includes an alkali-soluble resin (A), a compound (B) containing an ethylenically unsaturated group, a photoinitiator (C), a pigment (D) and an organic solvent (E). The photosensitive resin composition according to the present invention can improve linearity of pattern with high finesse and developing-resistance of the color filter.

Application of the study of reactivity of alkaline salts of isocyanuric acid to the synthesis of mono and trisubstituted isocyanurates

Reactivity of alkaline salts of isocyanuric acid has been studied. It has been established that the nucleophilic substitution is not selective because of the protonic exchanges between salts and substituted derivatives. The synthesis of mono or trisubstituted derivative is due to secondary reactions and to solvent effects. With this study, it has been possible to settle a method to prepare mono and trisubstituted derivatives of isocyanuric acid.

INTER- AND INTRAMOLECULAR REARRANGEMENTS OF CYANURIC ACID TRIALLYL ESTERS

It is shown that the catalytic and thermal rearrangements of cyanuric acid triallyl esters to isocyanuric acid esters proceed via inter- and intramolecular mechanisms.Cross-reaction products are formed when the reaction is carried out with a mixture of homologs, while the reaction in the presence of a hydroxy-containing compound gives its allyl ether and diallyl isocyanurate.

CATALYTIC REARRANGEMENT OF TRIS-(2-SUBSTITUTED-2-PROPENYL) CYANURATES.

Allyl esters of cyanuric and isocyanuric acids are widely used as cross-linking additives in order to confer thermal stability and heat resistance on polymeric materials. This paper is concerned with the synthesis and rearrangement of tris-(2-methyl-2-propenyl) (I), tris-(2-fluoro-2-propenyl) (II) and tris-(2-chloro-2-propenyl) (III) cyanurates. Experiments show that introduction of a substituent in position 2 of the allyl group retards the rearrangement reaction in comparison with triallyl cyanurate.

Investigation of the antitumor activity of new epoxide derivatives. I: s-Triazinetrione derivatives

The noteworthy cytostatic activity of triglycidyl-s-triazinetrione and the planned clinical testing of this new active substance induced us to subject this class of substances to closer examination. By chemical reaction of one of the three glycidyl groups present it was possible to introduce wide variations in the properties of the compounds, whilst still retaining the active principle. A number of these substances possessed very high antitumor activity as revealed in the leukemia screening test (P 388; mouse). The influence of other substituents within the glycidyl groups affecting the reactivity of the epoxide groups was also examined.