57137-33-4

Basic information

• Product Name: 2-(tert-butyldioxy)-4,6-dimethoxy-1,3,5-triazine
• Synonyms: 2-(tert-butyldioxy)-4,6-dimethoxy-1,3,5-triazine;2-[(1,1-Dimethylethyl)peroxy]-4,6-dimethoxy-1,3,5-triazine;Einecs 260-588-1
• CAS NO: 57137-33-4
• Molecular Formula: C₉H₁₅N₃O₄
• Molecular Weight: 229.2331
• EINECS: 260-588-1
• Mol File: 57137-33-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 311.3°Cat760mmHg
• Flash Point: 114.1°C
• Appearance: /
• Density: 1.163g/cm³
• Vapor Pressure: 0.00104mmHg at 25°C
• Refractive Index: 1.481
• CAS DataBase Reference: 2-(tert-butyldioxy)-4,6-dimethoxy-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(tert-butyldioxy)-4,6-dimethoxy-1,3,5-triazine(57137-33-4)
• EPA Substance Registry System: 2-(tert-butyldioxy)-4,6-dimethoxy-1,3,5-triazine(57137-33-4)

Safety Data

• Hazardous Substances Data: 57137-33-4(Hazardous Substances Data)

Usage

Physical form

White crystalline powder

Stability

Stable under normal conditions

Use as coupling agent

Facilitates the formation of strong and stable bonds between different molecules

Use as crosslinking agent

Used in the production of polymers and resins

Use as reagent

Particularly useful in the formation of carbon-carbon and carbon-nitrogen bonds.

InChI:InChI=1/C9H15N3O4/c1-9(2,3)16-15-8-11-6(13-4)10-7(12-8)14-5/h1-5H3

Upstream product

• 75-91-2 tert.-butylhydroperoxide 
• 3140-73-6 2-chloro-4,6-dimethoxy-1 ,3,5-triazine 

Relevant articles and documents

Organic Peroxides. Part 12. The Preparation and Properties of Some Triazinyl Peroxides

The triazinyl peroxides (A; X=Y=OOBut; X=OMe, Y=OOBut; X=Y=OMe; X=NEt2, Y=OOBut; X=Y=NEt2) and (B) have been prepared from the reaction between the appropriate peroxidic nucleophile and chlorotriazine.The structures of the peroxides are confirmed by their 13C n.m.r. spectra, and by the recovery of t-butyl hydroperoxide when the peroxides (A; X=Y=OOBut; X=OMe, Y=OOBut) were hydrolysed. .These peroxides are thermally stable up to ca. 90 deg C.Photolysis of the peroxides (A) gives the radical ButO. and XYC3N3O..The e.s.r. spectra of the triazinoxyl radicals could not be observed, but the adducts XYC3N3OCH2CH2. and XYC3N3OP.(OMe)3, which they form with ethylene and with trimethyl phosphite, respectively, were detected.It is suggested that these properties imply that the radicals have a ?-O rather than a ?-delocalised structure.