6294-79-7

Basic information

• Product Name: Diallyl Isocyanurate
• Synonyms: DIALLYL ISOCYANURATE;Hexahydro-1,3-diallyl-1,3,5-triazine-2,4,6-trione;1,3-diallylisocyanuric acid;1,3-Diallyl-1,3,5-triazinane-2,4,6-trione
• CAS NO: 6294-79-7
• Molecular Formula: C₉H₁₁N₃O₃
• Molecular Weight: 209.2
• Mol File: 6294-79-7.mol

Chemical Properties

• Melting Point: 145.0 to 150.0 °C
• Appearance: /
• Density: 1.213g/cm³
• Refractive Index: 1.515
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 6.65±0.20(Predicted)
• CAS DataBase Reference: Diallyl Isocyanurate(CAS DataBase Reference)
• NIST Chemistry Reference: Diallyl Isocyanurate(6294-79-7)
• EPA Substance Registry System: Diallyl Isocyanurate(6294-79-7)

Safety Data

• RTECS: XZ1835000
• Hazardous Substances Data: 6294-79-7(Hazardous Substances Data)

Usage

Uses

Used in Electrical Industry:
Diallyl Isocyanurate is used as a flame retardant and crosslinking agent in the electrical industry to enhance the safety and performance of electrical components and devices.
Used in Automotive Industry:
In the automotive industry, Diallyl Isocyanurate is utilized as a crosslinking agent in the production of plastics and polymers for automotive parts, contributing to their durability and flame resistance.
Used in Aerospace Industry:
Diallyl Isocyanurate is employed as a crosslinking agent in aerospace applications, providing high thermal stability and flame retardancy to materials used in aircraft and spacecraft components.
Used in Coatings and Adhesives:
Diallyl Isocyanurate serves as a curing agent in coatings and adhesives, improving their performance characteristics such as adhesion, durability, and resistance to environmental factors.
Used in Composite Materials:
As a component in resin systems for composite materials, Diallyl Isocyanurate enhances the mechanical properties and thermal stability of the final product, making it suitable for various applications.
Used as a Chemical Intermediate:
Diallyl Isocyanurate is also used as a chemical intermediate in the synthesis of other specialty chemicals, further expanding its applications in the chemical industry.
It is important to handle Diallyl Isocyanurate with caution due to its potential as a skin and eye irritant, as well as its potential to cause respiratory irritation and allergic reactions in sensitive individuals. Despite these precautions, its desirable properties and performance characteristics make it a valuable chemical in various industrial applications.

InChI:InChI=1/C9H11N3O3/c1-3-5-11-7(13)10-8(14)12(6-4-2)9(11)15/h3-4H,1-2,5-6H2,(H,10,13,14)

Upstream product

• 101-37-1 triallyl cyanurate 
• 108-80-5 cyanuric acid 
• 107-18-6 allyl alcohol 

Downstream Products

• 87709-09-9 1,3-diallyl-5-benzoylisocyanurate 
• 20395-16-8 1,3-diallyl-5-glycidyl isocyanurate 
• 5318-57-0 1,3-diallyl-5-octyl isocyanurate 
• 208850-41-3 1-benzoyl-3,5-bis(2,3-dibromopropyl)isocyanurate 

Relevant articles and documents

Production of [...]

A method for producing alkenyl isocyanurate by reacting cyanuric acid or isocyanuric acid with an unsaturated alcohol while in the presence of a palladium-loaded-activated-carbon catalyst. (Unsaturated alcohol example) R1-5: H, C1-20 alkyl, C6-20 aryl, C6-20 heterocyclic hydrocarbon; n: 1-4 (2-propen-1-ol, 3-buten-1-ol, 4-penten-1-ol, 5-hexen-1-ol, 2-buten-1-ol, 3-penten-2-ol, 2-methyl-2-propen-1-ol, and the like). (Example of palladium-loaded-activated-carbon catalyst) A zero-valent metal palladium, a bivalent palladium compound, or a catalyst obtained by loading activated carbon with these mixtures.

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.