5637-83-2

Basic information

• Product Name: 2,4,6-Triazido-s-triazine
• Synonyms: 2,4,6-Triazido-1,3,5-triazine;2,4,6-Triazido-s-triazine;Cyanuric triazide
• CAS NO: 5637-83-2
• Molecular Formula: C₃N₁₂
• Molecular Weight: 204.12
• Mol File: 5637-83-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 351.74°C (rough estimate)
• Appearance: /
• Density: 2.2785 (estimate)
• Refractive Index: 1.4000 (estimate)
• CAS DataBase Reference: 2,4,6-Triazido-s-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-Triazido-s-triazine(5637-83-2)
• EPA Substance Registry System: 2,4,6-Triazido-s-triazine(5637-83-2)

Safety Data

• Hazardous Substances Data: 5637-83-2(Hazardous Substances Data)

Usage

General Description

"2,4,6-Triazido-s-triazine" is a chemical compound with the molecular formula C3N9. It is a highly energetic and explosive material, often used as a component in high-energy materials and pyrotechnic mixtures. The compound has three azide (N3) groups attached to a central s-triazine ring, making it highly reactive and sensitive to shock, heat, or friction. Due to its explosive nature, it is used in military and industrial applications as a propellant, explosive filler, and initiator. Its chemical properties make it a valuable component in the production of high-impact and high-energy explosives. However, its instability and potential hazards make it extremely dangerous to handle and require strict safety precautions in its handling, storage, and transportation.

Upstream product

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

Downstream Products

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

Relevant articles and documents

-

-

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 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.