1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-tris[3-(trimethoxysilyl)propyl]-

Base Information

• Chemical Name: 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-tris[3-(trimethoxysilyl)propyl]-
• CAS No.: 26115-70-8
• Deprecated CAS: 701277-28-3,1387000-17-0,2645479-65-6,1387000-17-0
• Molecular Formula: C21H45N3O12Si3
• Molecular Weight: 615.858
• Hs Code.: 29336990
• European Community (EC) Number: 247-465-8
• UNII: V5YTB131U1
• DSSTox Substance ID: DTXSID2044896
• Nikkaji Number: J308.389F
• Wikidata: Q27291570
• ChEMBL ID: CHEMBL3188162
• Mol file: 26115-70-8.mol

Synonyms:26115-70-8;Tris(3-trimethoxysilylpropyl)isocyanurate;1,3,5-tris(3-(trimethoxysilyl)propyl)-1,3,5-triazinane-2,4,6-trione;1,3,5-tris(3-trimethoxysilylpropyl)-1,3,5-triazinane-2,4,6-trione;Tris[3-(trimethoxysilyl)propyl] isocyanurate;1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-tris[3-(trimethoxysilyl)propyl]-;tris(3-(trimethoxysilyl)propyl) isocyanurate;EINECS 247-465-8;UNII-V5YTB131U1;1,3,5-tris[3-(trimethoxysilyl)propyl]-1,3,5-triazinane-2,4,6-trione;V5YTB131U1;C21H45N3O12Si3;DTXSID2044896;1,3,5-Tris(gamma-trimethoxysilylpropyl)isocyanurate;1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-tris(3-(trimethoxysilyl)propyl)-;1,3,5-Tris(3-(trimethoxysilyl)propyl)-1,3,5-triazine-2,4,6(1H,3H,5H)-trione;1,3,5-tris[3-(trimethoxysilyl)propyl]-1,3,5-triazine-2,4,6(1H,3H,5H)-trione;SCHEMBL155052;CHEMBL3188162;DTXCID0024896;SILQUEST Y-19020 SILANE;Tox21_301284;MFCD00054746;AKOS024364961;C21-H45-N3-O12-Si3;FS-3995;SB73232;Tris(3-Trimethoxysilylpropyl)Iscyanurate;NCGC00256169-01;Tris[3-(Trimethoxysilyl)Propyl]Iscyanurate;CAS-26115-70-8;LS-155595;tris[3-(trimethoxysilyl)propyl]isocyanurate;CS-0199383;FT-0696801;I0602;1,3,5-tris(trimethoxysilylpropyl) isocyanurate;D91186;N,N',N"-Tris(3-trimethoxysilylpropyl)isocyanurate;J-016258;1,3,5-Tris(.gamma.-trimethoxysilylpropyl)isocyanurate;Q27291570;Isocyanuric Acid Tris[3-(trimethoxysilyl)propyl] Ester;TRIS(3-TRIMETHOXYSILYLPROPYL)CYCLOTRIISOCYANURATE;1,3,5-TRIS(3-(TRIMETHYOXYSILYL)PROPYL)ISOCYANURATE;2,4,6-TRIS(3-(TRIMETHOXYSILYL)PROPYL) ISOCYANURATE;Tris[3-(trimethoxysilyl)propyl] isocyanurate, technical grade;tris[3-(trimethoxysilyl)propyl]-1,3,5-triazinane-2,4,6-trione;S-TRIAZINE-2,4,6(1H,3H,5H)-TRIONE, 1,3,5-TRIS(3-(TRIMETHOXYSILYL)PROPYL)-

Chemical Property of 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-tris[3-(trimethoxysilyl)propyl]-

Chemical Property:

• Appearance/Colour: colorless to dark yellow liquid
• Vapor Pressure: 6.87E-12mmHg at 25°C
• Melting Point: <0°C
• Refractive Index: n20/D 1.461(lit.)
• Boiling Point: 543.9 °C at 760 mmHg
• PKA: -2.17±0.20(Predicted)
• Flash Point: 282.7 °C
• PSA: 149.07000
• Density: 1.131 g/cm³
• LogP: -0.02370
• Water Solubility.: 14-1000000000μg/L at 20℃
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 12
• Rotatable Bond Count: 21
• Exact Mass: 615.23110348
• Heavy Atom Count: 39
• Complexity: 636

Purity/Quality:

99.9% ^*data from raw suppliers

Tris[3-(trimethoxysilyl)propyl] Isocyanurate >95.0%(GC) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 23/25-36/38-68/20/21/22-42-21
• Safety Statements: 26-45-36/37-35-23

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Metals -> Metalloid Compounds (Silicon)
• Canonical SMILES: CO[Si](CCCN1C(=O)N(C(=O)N(C1=O)CCC[Si](OC)(OC)OC)CCC[Si](OC)(OC)OC)(OC)OC
• Uses: Adhesion promoter and cross-linking agent.Improves adhesion to PVC and a variety of substrates. Tris[3-(trimethoxysilyl)propyl] Isocyanurate is a cross-linking agent and an adhesion promoter that improves adhesion to PVS and variety of substrates. Tris[3-(trimethoxysilyl)propyl] isocyanurate (TTPI) can be used in the preparation of:Pd nanoparticle and single-walled carbon nanotube hybrid materials.Periodic mesoporous organosilicas exhibiting absorption properties for heavy metal ions like mercury.Mesoporous organosilica?alumina?composites with an affinity for CO2?gas at elevated temperatures.Isocyanurate-containing ordered mesoporous organosilicas using block copolymer.

Technology Process of 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-tris[3-(trimethoxysilyl)propyl]-

There total 6 articles about 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-tris[3-(trimethoxysilyl)propyl]- 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:

N-(3-trimethoxysilylpropyl) O-methyl carbamate (23432-62-4) → 3-(trimethoxysilyl)propyl isocyanate (15396-00-6) + tris-[3-(trimethoxysilyl)propyl]isocyanurate (26115-70-8)

Guidance literature:

at 210 ℃; for 1.65 - 5.65h; under 100 - 300 Torr; Product distribution / selectivity;

Reference yield:

N-(3-trimethoxysilylpropyl) O-methyl carbamate (23432-62-4) → tris-[3-(trimethoxysilyl)propyl]isocyanurate (26115-70-8)

Guidance literature:

With formic acid; sodium methylate; In methanol; at 130 - 214 ℃; for 0.5 - 1.75h; under 10 - 760.051 Torr; pH=5.6 - 10; Product distribution / selectivity;

Reference yield:

trimethoxysilane (2487-90-3) + triallyl isocyanurate (1025-15-6) → C18H35N3O9Si2 (26947-14-8) + C18H37N3O9Si2 + C21H45N3O12Si3 + tris-[3-(trimethoxysilyl)propyl]isocyanurate (26115-70-8)

Guidance literature:

With platinum⁽⁰⁾-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex; acetic acid; In toluene; at 53 - 55 ℃; for 2.5h; Temperature; Reagent/catalyst;

upstream raw materials:

N-(3-trimethoxysilylpropyl) O-methyl carbamate

3-(trimethoxysilyl)propan-1-amine

carbonic acid dimethyl ester

3-(trimethoxysilyl)propyl isocyanate

Refernces

• 1、 -. "COMPOSITION FOR RESIST UNDERLAYER FILM AND PROCESS FOR PRODUCING SAME". . . Retrieved 2010/06/22.
• 2、 -. "Process for making silylisocyanurate". Page/Page column 4. . Retrieved 2008/06/13.