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1,3,5-Tris(2-hydroxyethyl)isocyanurate / 50 G

Purity: 97 %
Synonym: Theic; 1,3,5-Tris(2-hydroxyethyl)cyanuric acid; 1,3,5-Tris(2-hydroxyethyl)-1,3,5-triazine-2,4,6(1H,3H,5H)-trione
Molecular Formula: C9H15N3O6
Molecular Weight: 261.23
SKU: MND-72115
CAS Number: 839-90-7
MDL number: MFCD00003549
EC Number: 212-660-9
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 50 G  
77.70 EUR


Properties

Flash Point (C)241 °C - open cup
Flash Point (F)465.8 °F - open cup
Melting Point136-140 °C (lit.)

 Product Description

1,3,5-Tris(2-hydroxyethyl)isocyanurate is a chemical compound commonly used as a crosslinking agent and flame retardant in the production of polyurethane foams and coatings. It contains three hydroxyethyl groups attached to an isocyanurate ring structure.

 

Application:

1,3,5-Tris(2-hydroxyethyl)isocyanurate serves as a crosslinking agent in the synthesis of polyurethane foams, coatings, and adhesives, enhancing their strength and durability. It is also employed as a flame retardant additive, improving the fire resistance of various polymeric materials.

 

 

 

Articles:

- New Hydrogen-Bond-Enriched 1,3,5-Tris(2-hydroxyethyl) Isocyanurate Covalently Functionalized MCM-41: An Efficient and Recoverable Hybrid Catalyst for Convenient Synthesis of Acridinedione Derivatives

Publication Date: November 12, 2019

Zahra Alirezvani, Mohammad G. Dekamin and Ehsan Valiey

https://doi.org/10.1021/acsomega.9b02755

 

- Dendrons containing boric acid and 1,3,5-tris(2-hydroxyethyl)isocyanurate covalently attached to silica-coated magnetite for the expeditious synthesis of Hantzsch esters

Publication Date: 27 January 2021

Mahsa Sam, Mohammad G. Dekamin & Zahra Alirezvani

https://doi.org/10.1038/s41598-020-80884-z

 

- 1,3,5-Tris(2-hydroxyethyl)isocyanurate functionalized graphene oxide: a novel and efficient nanocatalyst for the one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones

Publication Date: 13 Jun 2017

Mohammad G. Dekamin, Fatemeh Mehdipoora and Amene Yaghoubia 

https://doi.org/10.1039/C7NJ00632B