36196-44-8

Basic information

• Product Name: TRIS[2-(3-MERCAPTOPROPIONYLOXY)ETHYL] ISOCYANURATE
• Synonyms: TRIS[2-(3-MERCAPTOPROPIONYLOXY)ETHYL] ISOCYANURATE;propanoicacid,3-mercapto-,(2,4,6-trioxo-1,3,5-triazine-1,3,5(2h,4h,6h)-triyl;propanoicacid,3-mercapto-,(2,4,6-trioxo-1,3,5-triazine-1,3,5(2h,4h,6h)-triyl)tri-2,1-ethanediylester;Propanoicacid,3-mercpto-,[2,4,6-trioxo-1,3,5-triazine-1,3,5(2H,4H,6H)-triyl]tri-2,1-ethanediylester;(2,4,6-trioxo-1,3,5-triazine-1,3,5(2H,4H,6H)-triyl)triethane-2,1-diyl tris(3-mercaptopropionate);1,3,5-Tris[2-(3-mercaptopropionyloxy)ethyl]-1,3,5-triazine-2,4,6(1H,3H,5H)-trione;Tris(3-mercaptopropanoic acid)[2,4,6-trioxo-1,3,5-triazine-1,3,5(2H,4H,6H)-triyl]tri(2,1-ethanediyl) ester;3TI
• CAS NO: 36196-44-8
• Molecular Formula: C₁₈H₂₇N₃O₉S₃
• Molecular Weight: 525.62
• EINECS: 252-907-8
• Product Categories: Building Blocks;Chemical Synthesis;Crosslinkers;Heterocyclic Building Blocks;Materials Science;Polymer Additives;Polymer Science;Triazines
• Mol File: 36196-44-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 681.1°Cat760mmHg
• Flash Point: >110°C
• Appearance: /
• Density: 1.333g/mLat 25℃
• Vapor Pressure: 2.1E-18mmHg at 25°C
• Refractive Index: n20/D 1.538
• Storage Temp.: 2-8°C
• PKA: 9.15±0.10(Predicted)
• Water Solubility: 1.61g/L at 20℃
• CAS DataBase Reference: TRIS[2-(3-MERCAPTOPROPIONYLOXY)ETHYL] ISOCYANURATE(CAS DataBase Reference)
• NIST Chemistry Reference: TRIS[2-(3-MERCAPTOPROPIONYLOXY)ETHYL] ISOCYANURATE(36196-44-8)
• EPA Substance Registry System: TRIS[2-(3-MERCAPTOPROPIONYLOXY)ETHYL] ISOCYANURATE(36196-44-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/39
• Hazardous Substances Data: 36196-44-8(Hazardous Substances Data)

Usage

General Description

TRIS[2-(3-MERCAPTOPROPIONYLOXY)ETHYL] ISOCYANURATE is a specialty chemical denoted as a sulfur-containing triazinetrione. TRIS[2-(3-MERCAPTOPROPIONYLOXY)ETHYL] ISOCYANURATE is primarily used as a crosslinking agent due to its high reactivity toward polymers. The substance contains three mercaptopropionyloxy groups linked to an isocyanurate ring which drives its reactivity and functional properties. The mercaptopropionyl groups can interact with a variety of substrates to form covalent linkages, enabling the production of diverse crosslinked materials with enhanced mechanical and thermal resistance. Moreover, the isocyanurate ring in this chemical imparts additional thermal stability. This makes it potentially useful in a myriad of applications from adhesives and coatings to rubber and plastics.

InChI:InChI=1/C18H27N3O9S3/c22-13(1-10-31)28-7-4-19-16(25)20(5-8-29-14(23)2-11-32)18(27)21(17(19)26)6-9-30-15(24)3-12-33/h31-33H,1-12H2

Upstream product

• 839-90-7 1,3,5-tris(2-hydroxyethyl)-S-triazine-2,4,6-trione 
• 107-96-0 3-mercaptopropionic acid 

Relevant articles and documents

Activated dopamine derivatives as primers for adhesive-patch fixation of bone fractures

For the stabilization of complex bone fractures, tissue adhesives are an attractive alternative to conventional implants, often consisting of metal plates and screws whose fixation may impose additional trauma on the already fractured bone. This study reports on the synthesis and evaluation of activated dopamine derivatives as primers for fiber-reinforced-adhesive patches in bone-fracture stabilization strategies. The performance of synthesized dopamine derivatives are evaluated with regard to the adhesive shear strength of formed bone patches, as well as cell viability and surface properties. Dopamine-derived primers with methacrylamide, allyl, and thiol functional groups were found to significantly increase the adhesive shear strength of adhesive patches. Furthermore, deprotonation of the primer solution was determined to be essential in order to achieve good adhesion. In conclusion, the primer solutions that were found to give the best adhesion were the once where dopa-thiol was used in combination with either dopa-methacrylamide or dopa-allyl, resulting in shear bond strengths of 0.29 MPa.