16268-92-1

Basic information

• Product Name: N,N',N''-triethyl-1,3,5-triazine-2,4,6-triamine
• Synonyms: N,N',N''-triethyl-1,3,5-triazine-2,4,6-triamine;N2,N4,N6-triethyl-1,3,5-triazine-2,4,6-triaMine;TriethylMelaMine;2,4,6-tris-ethylamino-(1,3,5)triazine
• CAS NO: 16268-92-1
• Molecular Formula: C₉H₁₈N₆
• Molecular Weight: 210.27942
• EINECS: 240-372-3
• Mol File: 16268-92-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 339.81°C (rough estimate)
• Flash Point: 181.7°C
• Appearance: /
• Density: 1.1756 (rough estimate)
• Refractive Index: 1.7900 (estimate)
• Water Solubility: 1.539g/L(25 oC)
• CAS DataBase Reference: N,N',N''-triethyl-1,3,5-triazine-2,4,6-triamine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N',N''-triethyl-1,3,5-triazine-2,4,6-triamine(16268-92-1)
• EPA Substance Registry System: N,N',N''-triethyl-1,3,5-triazine-2,4,6-triamine(16268-92-1)

Safety Data

• Hazardous Substances Data: 16268-92-1(Hazardous Substances Data)

Usage

Uses

Triethylmelamine, can be used as a chemosterilants of houseflies.

Upstream product

• 108-78-1 2,4,6-triamino-s-triazine 
• 64-17-5 ethanol 
• 75-04-7 ethylamine 
• 5759-58-0 2,4,6-tris(methylthio)-1,3,5-triazine 
• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 122-34-9 Simazine 

Downstream Products

• 75-04-7 ethylamine 
• 108-80-5 isocyanuric acid 

Relevant articles and documents

METHOD FOR ALKYLATING AN AMINO COMPOUND

The invention relates to a method for alkylating an amino compound, characterized in that at least one triazine derivative of general formula (I) or at least one urea or urea derivative of the general formula (II), (II), wherein ? R4 and R5 mean independently from each other Q1 or a moiety of the formula R6-N-R7 or R8-N-R9 bound with its central nitrogen atom to the triazine ring of the structure of formula (I), whereat - Q1 means a linear or branched C1-C30-alkyl or a cyclic substituent in form of a C5-C20-cycloalkyl, a C5-C20-aryl, a C1-C20-alkylsubstituted C5-C20-aryl or an amide of a cyclic unsaturated carboxylic acid, whereat the C1-C30-alkyl or the cyclic substituent can be interrupted by one or multiple oxygen atoms, sulphur atoms, substituted nitrogen atoms and/or by one or multiple groups of the type –C(O)O-,-OC(O)-,-C(O)- and/or –OC(O)O-, ? R1, R2, R3, R6, R7, R8 and R9 mean independently from each other H, linear or branched C1-C20-alkyl, C5-C20-cyclo alkyl, C5-C20-aryl, C1-C20-alkylsubstituted C5-C20-aryl, which in each case can be interrupted by one or multiple oxygen atoms, sulphur atoms and/or substituted nitrogen atoms and/or by one or multiple groups of the type –C(O)O-, - OC(O)-, -C(O)- and/or –OC(O) O- and/or can be functionalized by one or multiple hydroxyl groups and/or mercapto groups, and ? X means O or S, is reacted with at least one alcohol of the general formula (III) R10-OH wherein R10 means a linear or branched C1-C20-alkyl, C5-C20-cycloalkyl, or C1-C20- alkylsubstituted C5-C20-aryl, which can be in each case interrupted by one or multiple oxygen atoms, sulphur atoms, substituted nitrogen atoms and/or by one or multiple groups of the type –C(O)O-, -OC(O)-, -C(O)- and/or –OC(O)O- and/or can be functionalized by one or multiple hydroxyl groups and/or mercapto groups, wherein the reaction is carried out in the presence of at least one Ruthenate of the general formula (IV) Mn(RuO4) and/or at least one Perruthenate of the general formula (V) M(RuO4)n wherein the cation M is selected from a group comprising an alkali, earth alkali or substituted or non-substituted ammonium cation.