82124-01-4

Basic information

• Product Name: 1,3,5-triazine-2,4,6-triamine oxalate
• Synonyms: 1,3,5-triazine-2,4,6-triamine oxalate;1,3,5-Triazine-2,4,6-triamine/oxalic acid,(1:x);Einecs 279-902-3
• CAS NO: 82124-01-4
• Molecular Formula: C5H8N6O4
• Molecular Weight: 216.15482
• EINECS: 279-902-3
• Mol File: 82124-01-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 785.6°Cat760mmHg
• Flash Point: 428.9°C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: 1,3,5-triazine-2,4,6-triamine oxalate(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-triazine-2,4,6-triamine oxalate(82124-01-4)
• EPA Substance Registry System: 1,3,5-triazine-2,4,6-triamine oxalate(82124-01-4)

Safety Data

• Hazardous Substances Data: 82124-01-4(Hazardous Substances Data)

Usage

Appearance

White, crystalline powder

Solubility

Soluble in water

Uses

Manufacturing of melamine-formaldehyde resins, flame retardants, and adhesives; nitrogen-rich fertilizer; stabilizer in the food industry; component in the production of pharmaceuticals and plastics

Industrial applications

High nitrogen content and ability to form strong and durable compounds

Safety

Exposure can be harmful; precautions should be taken for safe handling and use

Upstream product

• 108-78-1 2,4,6-triamino-s-triazine 
• 144-62-7 oxalic acid 

Relevant articles and documents

Using Desmotropes, Cocrystals, and Salts to Manipulate Reactivity in Mechanochemical Organic Reactions

Performing reactions in the solid state offers the largely unexplored possibility of influencing reactivity by manipulating the solid form of the starting reactants. In this work, we explore the use of various solid forms of barbituric acid and its effect on reaction paths and kinetics in a Knoevenagel condensation reaction with vanillin. Modifications of barbituric acid included the use of its desmotrope, a cocrystal, and a salt as the starting reactant. Comparing these reactions with the reaction starting from the commercial keto tautomer of barbituric acid, we find that the reaction kinetics could be accelerated or decelerated, together with a change in the reaction mechanism. Exploring solid forms of reactants can be used as general methodology for manipulating mechanochemical reactivity, further highlighting the benefits of conducting reactions in the solid state, because many of the modifications of solids become unavailable upon dissolution.