5637-83-2

Usage

Uses

Used in Military and Industrial Applications:
2,4,6-Triazido-s-triazine is used as a propellant for its high energy release, making it suitable for applications requiring rapid propulsion, such as in missiles and rockets.
2,4,6-Triazido-s-triazine is used as an explosive filler for its high explosive power, utilized in the production of high-impact explosives for demolition and construction purposes.
2,4,6-Triazido-s-triazine is used as an initiator due to its sensitivity to shock, heat, or friction, making it ideal for triggering the detonation process in various explosive devices.
Used in High-Energy Materials Production:
2,4,6-Triazido-s-triazine is used as a key component in the formulation of high-energy materials, contributing to their high energy density and performance in applications such as propellants and explosives.
Due to the compound's instability and potential hazards, strict safety precautions are necessary in its handling, storage, and transportation to mitigate risks associated with its explosive nature.

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 

Downstream Products

• 108-80-5 isocyanuric acid 
• 460-19-5 ethanedinitrile 
• 108-78-1 2,4,6-triamino-s-triazine 

Relevant academic research and scientific papers

Improving stability of the metal-free primary energetic cyanuric triazide (CTA) through cocrystallization

Cyanuric triazide (CTA) and benzotrifuroxan (BTF) form a metal-free primary energetic cocrystal with suppressed volatility and improved thermal properties relative to CTA. Though electrostatic potential maps of the most stable conformations do not predict favorable interactions, a higher energy conformer has appropriate electrostatics and is selected by BTF in the cocrystal.

Organocatalytic Enamine–Azide Addition Reaction in the Synthesis of 1,4,5-Trisubstituted 1,2,3-Triazoles

Abstract: A high efficiency of diethanolamine as organocatalyst in the cycloaddition of organic (including heterocyclic) mono-, di-, and triazides to active methylene compounds has been demonstrated. As a result, a number of functionally substituted bi- a

Synthesis of azidopropargylamino-substituted 1,3,5-triazines – novel monomers for the production of energetic polymers

[Figure not available: see fulltext.] Efficient methods for the synthesis of novel azidopropargylamino-substituted 1,3,5-triazines were developed. 4,6-Diazido-N-(prop-2-yn-1-yl)-1,3,5-triazin-2-amine was obtained by the method of sequential nucleophilic substitution of chlorine atoms in cyanuric chloride by amino and azido groups or by the method of selective substitution of the azido group in triazidotriazine with propargylamine. 6-Azido-N2,N4-dimethyl-N2,N4-di(prop-2-yn-1-yl)-1,3,5-triazine-2,4-diamine was obtained by nitrosation of the corresponding 6-hydrazinyl-N2,N4-dimethyl-N2,N4-di(prop-2-yn-1-yl)-1,3,5-triazine-2,4-diamine. Monomers with a lower melting point were obtained by N-methylation of azidopropargylamino-substituted 1,3,5-triazines.

Synthesis and unique photoluminescence properties of nitrogen-rich quantum dots and their applications

Nitrogen-rich quantum dots (N-dots) were serendipitously synthesized in methanol or aqueous solution at a reaction temperature as low as 50 °C. These N-dots have a small size (less than 10 nm) and contain a high percentage of the element nitrogen, and are thus a new member of quantumdot family. These N-dots show unique and distinct photoluminescence properties with an increasing percentage of nitrogen compared to the neighboring carbon dots. The photoluminescence behavior was adjusted from blue to green simply through variation of the reaction temperature. Furthermore, the detailed mechanism of N-dot formation was also proposed with the trapped intermediate. These N-dots have also shown promising applications as fluorescent ink and biocompatible staining in C. elegans.