CAS 760952-88-3

THPTA

Triazole Ligands & Catalysts

About This Compound

Triazole-containing ligands are specialized additives designed to accelerate and stabilize Cu(I)-catalyzed click reactions. THPTA, BTTAA, and related polytriazole ligands coordinate Cu(I) ions, preventing oxidative degradation while maintaining catalytic activity. These ligands are essential for performing CuAAC in aqueous media and biological systems, where unprotected Cu(I) would rapidly generate reactive oxygen species that damage proteins and nucleic acids.

Related Reactions: CuAAC
Molecular FormulaC18H30N10O3 Molecular Weight434.501 g/mol InChIKeyVAKXPQHQQNOUEZ-UHFFFAOYSA-N CAS Registry760952-88-3 Literature Refs143 references

Synthesis Routes

Showing 3 of 25 available routes, sorted by yield.

Route 1

1 step Yield: 100%
tris(3-acetoxypropyltriazolylmethyl)amine
CAS 1208358-31-9
C24H36N10O6
THPTA
Conditions With ammonia In methanol at 40℃;
Reference Post, Elias A. J.; Fletcher, Stephen P. [Journal of Organic Chemistry, 2019, vol. 84, # 5, p. 2741 - 2755] DOI
Source Reaxys

Route 2

1 step Yield: 90%
C24H27N5O13
C24H27N5O13
+
1,11-bis(2-propyn-1-oxy)-3,6,9-trioxaundecane
CAS 159428-42-9
C14H22O5
+
THPTA
CAS 760952-88-3
C18H30N10O3
THPTA
Conditions With copper(ll) sulfate pentahydrate; (+)-sodium L-ascorbate In methanol; water at 20℃;
Reference Current Patent Assignee: NANKAI UNIVERSITY - CN119977917, 2025, A Location in patent: Paragraph 0048-0050; 0054-0055
Source Reaxys

Route 3

1 step Yield: 90%
tripopargylamine
CAS 6921-29-5
C9H9N
+
3-azidopropan-1-ol
CAS 72320-38-8
C3H7N3O
THPTA
Conditions With biocompatible Cu(I)/melanin dot-based catalyst In aq. phosphate buffer for 0.5h;
Reference Sun, Yao; Hong, Suhyun; Ma, Xiaowei; Cheng, Kai; Wang, Jing; Zhang, Zhe; Yang, Meng; Jiang, Yuxin; Hong, Xuechuan; Cheng, Zhen [Chemical Science, 2016, vol. 7, # 9, p. 5888 - 5892] DOI
Source Reaxys
22 additional routes available in the full dataset. Contact us for complete synthesis route data.

Related Compounds

Other Triazole Ligands & Catalysts in our catalog:

Frequently Asked Questions

Why do I need a triazole ligand for CuAAC in biological systems?

Cu(I) ions in aqueous solution rapidly react with dissolved oxygen to produce Cu(II) and reactive oxygen species (ROS), which oxidatively damage proteins, DNA, and lipids. Triazole ligands like THPTA and BTTAA tightly chelate Cu(I), shielding it from oxygen while maintaining its catalytic activity. This reduces biomolecular damage by >90% compared to ligand-free CuAAC.

What is the optimal ligand-to-copper ratio?

For THPTA, a 2:1 or 3:1 ligand:Cu ratio is standard (e.g., 1.8 mM THPTA with 0.9 mM CuSO₄). For BTTAA, a 3:1 ratio is recommended. Excess ligand ensures complete Cu(I) coordination but very high concentrations may inhibit the reaction by over-stabilizing Cu(I) and reducing its reactivity with the azide.

Can I use THPTA for in vivo click chemistry?

THPTA is suitable for cell-surface labeling and extracellular applications but has limited cell permeability. For intracellular CuAAC, BTTAA offers better biocompatibility, though copper-free methods (SPAAC, IEDDA) are generally preferred for live-cell applications. THPTA has been successfully used for zebrafish embryo labeling at low Cu concentrations.

How should I store triazole ligand solutions?

Stock solutions of THPTA or BTTAA (10–100 mM in DMSO or water) can be stored at −20 °C for several months. Avoid repeated freeze-thaw cycles. Working solutions (1–10 mM) should be prepared fresh or stored at 4 °C for up to one week. The ligands are stable at room temperature as solids.

Last updated: July 27, 2026