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Technology Process of N~2~,N~2~,N~4~,N~4~,N~6~,N~6~-Hexamethoxy-1,3,5-triazine-2,4,6-triamine

N~2~,N~2~,N~4~,N~4~,N~6~,N~6~-Hexamethoxy-1,3,5-triazine-2,4,6-triamine

Base Information
  • Chemical Name:N~2~,N~2~,N~4~,N~4~,N~6~,N~6~-Hexamethoxy-1,3,5-triazine-2,4,6-triamine
  • CAS No.:39863-30-4
  • Molecular Formula:C9H18N6O6
  • Molecular Weight:306.27600
  • Hs Code.:3909200000
  • DSSTox Substance ID:DTXSID30597094
  • Nikkaji Number:J1.592.621J
  • Wikidata:Q82492572
  • Mol file:39863-30-4.mol
N~2~,N~2~,N~4~,N~4~,N~6~,N~6~-Hexamethoxy-1,3,5-triazine-2,4,6-triamine

Synonyms:39863-30-4;2-N,2-N,4-N,4-N,6-N,6-N-hexamethoxy-1,3,5-triazine-2,4,6-triamine;N~2~,N~2~,N~4~,N~4~,N~6~,N~6~-Hexamethoxy-1,3,5-triazine-2,4,6-triamine;hexamethoxymelamine;SCHEMBL561793;DTXSID30597094

Suppliers and Price of N~2~,N~2~,N~4~,N~4~,N~6~,N~6~-Hexamethoxy-1,3,5-triazine-2,4,6-triamine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 11 raw suppliers
Chemical Property of N~2~,N~2~,N~4~,N~4~,N~6~,N~6~-Hexamethoxy-1,3,5-triazine-2,4,6-triamine
Chemical Property:
  • Boiling Point:349.8±25.0 °C(Predicted) 
  • PKA:5.71±0.10(Predicted) 
  • PSA：169.77000 
  • Density:1.384±0.06 g/cm3(Predicted) 
  • LogP:-4.01040 
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:12
  • Rotatable Bond Count:9
  • Exact Mass:306.12878232
  • Heavy Atom Count:21
  • Complexity:223
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CON(C1=NC(=NC(=N1)N(OC)OC)N(OC)OC)OC
  • uses Hexamethylolmelamine can further condense in the presence of an acid catalyst; ether linkages can also form (see “Urea Formaldehyde”). A wide variety of resins can be obtained by careful selection of pH, reaction temperature, reactant ratio, amino monomer, and extent of condensation. Liquid coating resins are prepared by reacting methanol or butanol with the initial methylolated products. These can be used to produce hard, solvent-resistant coatings by heating with a variety of hydroxy, carboxyl, and amide functional polymers to produce a cross-linked film.
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