Date published: 2026-2-1

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Triethyl 1,3,5-triazine-2,4,6-tricarboxylate (CAS 898-22-6)

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CAS Number:
898-22-6
Molecular Weight:
297.26
Molecular Formula:
C12H15N3O6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Triethyl 1,3,5-triazine-2,4,6-tricarboxylate, known as TETA, is a chemical compound belonging to the triazine class. Its extensive usage spans diverse fields, including chemical synthesis and polymer chemistry. Triethyl 1,3,5-triazine-2,4,6-tricarboxylate has served as a chelating agent, effectively forming stable complexes with metal ions. Moreover, it has found application as a crosslinking agent in polymer synthesis, facilitating the formation of covalent bonds between polymer chains. This results in the development of a three-dimensional network that enhances the mechanical and thermal properties of the polymer. Furthermore, Triethyl 1,3,5-triazine-2,4,6-tricarboxylate acts as a precursor for synthesis. Its notable affinity for divalent and trivalent metal ions, such as copper, zinc, and iron, contributes to its chelating capabilities.


Triethyl 1,3,5-triazine-2,4,6-tricarboxylate (CAS 898-22-6) References

  1. Design and synthesis of 'dumb-bell' and 'triangular' inorganic-organic hybrid nanopolyoxometalate clusters and their characterisation through ESI-MS analyses.  |  Pradeep, CP., et al. 2011. Chemistry. 17: 7472-9. PMID: 21594915
  2. Reaction of Aldehydes/Ketones with Electron-Deficient 1,3,5-Triazines Leading to Functionalized Pyrimidines as Diels-Alder/Retro-Diels-Alder Reaction Products: Reaction Development and Mechanistic Studies.  |  Yang, K., et al. 2017. J Org Chem. 82: 2336-2344. PMID: 28112917
  3. Acyclic and Heterocyclic Azadiene Diels-Alder Reactions Promoted by Perfluoroalcohol Solvent Hydrogen Bonding: Comprehensive Examination of Scope.  |  Zhu, Z. and Boger, DL. 2022. J Org Chem. 87: 14657-14672. PMID: 36239452
  4. Dienophilicity of imidazole in inverse electron demand Diels–Alder reactions: cycloadditions with 1,2,4,5-tetrazines and the structure of zarzissine  |  Zhao-Kui Wan, Grace H.C. Woo, John K. Snyder. 2001. Tetrahedron. 57: 5497-5507.
  5. Exploring the Route to 1,3,5-Triazine-2,4,6-triisocyanate (C6N6O3), a Hydrogen-Free Molecular Precursor for Polymeric C–N–(O) Materials  |  Carsten Ludwig Schmidt, Martin Jansen. 2012. European Journal of Organic Chemistry. 2012: 5649-5657.
  6. Synthesis of semi-saturated polycyclic 1,2,4-triazoles from lactams  |  Sierra C. Nguyen, Allen Y. Hong. 2021. Tetrahedron Letters. 82.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Triethyl 1,3,5-triazine-2,4,6-tricarboxylate, 5 g

sc-255696
5 g
$218.00