Triglycidyl cyanurate

Base Information

• Chemical Name: Triglycidyl cyanurate
• CAS No.: 2589-01-7
• Molecular Formula: C12H15 N3 O6
• Molecular Weight: 297.268
• Hs Code.: 2933699090
• European Community (EC) Number: 219-974-5
• NSC Number: 59090
• DSSTox Substance ID: DTXSID40948790
• Nikkaji Number: J40.131E
• Mol file: 2589-01-7.mol

Synonyms:Triglycidyl cyanurate;2589-01-7;1,3,5-Triazine, 2,4,6-tris(oxiranylmethoxy)-;Cyanuric acid triglycidyl ester;2,4,6-tris(oxiran-2-ylmethoxy)-1,3,5-triazine;EINECS 219-974-5;2,4,6-Tris(glycidyloxy)-s-triazine;NSC 59090;BRN 0762505;2,4,6-Tris(oxiranylmethoxy)-1,3,5-triazine;s-Triazine, 2,4,6-tris(2,3-epoxypropoxy)-;s-Triazine-2,4,6-triol, tri(2,3-epoxypropyl) ester;SCHEMBL487480;Cyanuric acid, triglycidyl ester;DTXSID40948790;2,6-Tris(glycidyloxy)-s-triazine;NSC59090;NSC-59090;s-Triazine,4,6-tris(2,3-epoxypropoxy)-;LS-155581;1,5-Triazine, 2,4,6-tris(oxiranylmethoxy)-;s-Triazine-2,6-triol, tri(2,3-epoxypropyl) ester;2,4,6-Tris[(oxiran-2-yl)methoxy]-1,3,5-triazine;WLN: T6N CN ENJ BO1- BT3OTJ& DO1- BT3OTJ& FO1- BT3OTJ

Chemical Property of Triglycidyl cyanurate

Chemical Property:

• Vapor Pressure: 6.26E-10mmHg at 25°C
• Refractive Index: 1.5290 (estimate)
• Boiling Point: 507.7°Cat760mmHg
• Flash Point: 179.9°C
• PSA: 103.95000
• Density: 1.471g/cm³
• LogP: -0.79560
• XLogP3: 0
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 9
• Exact Mass: 297.09608521
• Heavy Atom Count: 21
• Complexity: 298

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(O1)COC2=NC(=NC(=N2)OCC3CO3)OCC4CO4

Technology Process of Triglycidyl cyanurate

There total 2 articles about Triglycidyl cyanurate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

1,3,5-trichloro-2,4,6-triazine (108-77-0) + oxiranyl-methanol (556-52-5) → 2,4,6-tris(glycidyl)-1,3,5-triazine (2589-01-7)

Guidance literature:

With sodium hydride; Yield given. Multistep reaction; 1.) benzene, toluene, 6 h, 2.a) toluene, r.t., 1 h, b) 45 deg C, 1 h, c) reflux, overnight;

DOI:10.1002/oms.1210271107

Reference yield:

→ 2,4,6-tris(glycidyl)-1,3,5-triazine (2589-01-7)

Guidance literature:

Cyanursaeure, Epichlorhydrin;

upstream raw materials:

1,3,5-trichloro-2,4,6-triazine

oxiranyl-methanol

Refernces