6291-95-8

Basic information

• Product Name: TRIMETHALLYL ISOCYANURATE
• Synonyms: TRIMETHALLYL ISOCYANURATE;1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-tris(2-methyl-2-propenyl)-;1,3,5-Tris(2-methyl-2-propenyl)-1,3,5-triazine-2,4,6(1H,3H,5H)-trione;1,3,5-Tris(2-methylallyl)-1,3,5-triazine-2,4,6(1H,3H,5H)-trione;1,3,5-tris(2-methyl-2-propen-1-yl)-1,3,5-Triazine-2,4,6(1H,3H,5H)-trione;1,3,5-Tris(2-methylallyl)-1,3,5-triazinane-2,4,6-trione
• CAS NO: 6291-95-8
• Molecular Formula: C₁₅H₂₁N₃O₃
• Molecular Weight: 291.35
• Product Categories: monomer
• Mol File: 6291-95-8.mol
• Article Data: 5

Chemical Properties

• Melting Point: 85-86 °C
• Boiling Point: 402.7°C at 760 mmHg
• Flash Point: 163.4°C
• Appearance: /
• Density: 1.097g/cm³
• Vapor Pressure: 1.08E-06mmHg at 25°C
• Refractive Index: 1.509
• PKA: -2.41±0.20(Predicted)
• CAS DataBase Reference: TRIMETHALLYL ISOCYANURATE(CAS DataBase Reference)
• NIST Chemistry Reference: TRIMETHALLYL ISOCYANURATE(6291-95-8)
• EPA Substance Registry System: TRIMETHALLYL ISOCYANURATE(6291-95-8)

Safety Data

• Statements: 20/21/22-36/37/38
• Safety Statements: 22-26-36/37/39
• RIDADR: 2811
• Hazardous Substances Data: 6291-95-8(Hazardous Substances Data)

Usage

General Description

Trimethallyl isocyanurate is a chemical compound with the molecular formula C12H15N3O3. It is commonly used as a crosslinking agent in the production of various materials, such as coatings, adhesives, and thermosetting resins. Trimethallyl isocyanurate is known for its excellent thermal and chemical resistance, as well as its ability to improve the mechanical properties of the materials it is added to. Due to its versatility and effectiveness as a crosslinking agent, trimethallyl isocyanurate is widely used in industries such as automotive, aerospace, and construction. However, it is important to handle this chemical with care, as it may cause irritation or allergic reactions upon contact with skin or inhalation.

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 articles and documents

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.

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.

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.