Triglycidyl Isocyanurate

• CAT Number: R029705
• CAS Number: 2451-62-9
• Molecular Formula: C12H15N3O6
• Molecular Weight: 297.27
• Purity: ≥95%
• Synonyms: 1,3,5-Triglycidyl isocyanurate; 1,3,5-Triglycidyl-s-triazine-2,4,6-trione; 1,3,5-Triglycidylhexahydro-1,3,5-triazine-2,4,6-trione; 1,3,5-Triglycidylisocyanuric acid; 1,3,5-Tris(2,3-epoxypropyl) isocyanurate; 1,3,5- Tris(oxiran-2-ylmethyl)-1,3,5-triaz
• Target: MDM-2/p53
• Storage: -20°C
• IUPAC Name: 1,3,5-tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione
• InChI: InChI=1S/C12H15N3O6/c16-10-13(1-7-4-19-7)11(17)15(3-9-6-21-9)12(18)14(10)2-8-5-20-8/h7-9H,1-6H2
• InChIKey: OUPZKGBUJRBPGC-UHFFFAOYSA-N
• SMILES: C1C(O1)CN2C(=O)N(C(=O)N(C2=O)CC3CO3)CC4CO4

Triglycidyl Isocyanurate (TGIC) (Cat No.: R029705) is a chemical compound commonly used as a crosslinking agent in the production of powder coatings and plastic materials. It reacts with various resins to improve the durability, heat resistance, and chemical stability of coatings. TGIC also plays a role in enhancing the mechanical properties of polymers. However, it is considered a potential health hazard due to its toxicity and may pose risks during handling and manufacturing, prompting the need for protective measures in industrial settings. Triglycidyl isocyanurate can be used for cancer research.

Reference

1.Di, Y., and R. J. Heath. "Collagen stabilization and modification using a polyepoxide, triglycidyl isocyanurate." Polymer Degradation and Stability 94.10 (2009): 1684-1692.
2.Wu, Kun, et al. "Flame retardant effect of polyhedral oligomeric silsesquioxane and triglycidyl isocyanurate on glass fibre‐reinforced epoxy composites." Polymer composites 32.3 (2011): 378-389.
3.Xing, Weiyi, et al. "Flame retardancy and thermal degradation of cotton textiles based on UV-curable flame retardant coatings." Thermochimica acta 513.1-2 (2011): 75-82.