5118-79-6

Basic information

• Product Name: 6,6'-(2,1-Phenylene)bis(1,3,5-triazine-2,4-diamine)
• Synonyms: 6,6'-(1,2-Phenylene)bis(1,3,5-triazine-2,4-diamine);6,6'-(2,1-Phenylene)bis(1,3,5-triazine-2,4-diamine);Phthaloguanamine
• CAS NO: 5118-79-6
• Molecular Formula: C₁₂H₁₂N₁₀
• Molecular Weight: 296.2907
• Mol File: 5118-79-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 834.1°Cat760mmHg
• Flash Point: 502.3°C
• Appearance: /
• Density: 1.572g/cm³
• CAS DataBase Reference: 6,6'-(2,1-Phenylene)bis(1,3,5-triazine-2,4-diamine)(CAS DataBase Reference)
• NIST Chemistry Reference: 6,6'-(2,1-Phenylene)bis(1,3,5-triazine-2,4-diamine)(5118-79-6)
• EPA Substance Registry System: 6,6'-(2,1-Phenylene)bis(1,3,5-triazine-2,4-diamine)(5118-79-6)

Safety Data

• Hazardous Substances Data: 5118-79-6(Hazardous Substances Data)

Usage

General Description

6,6'-(2,1-Phenylene)bis(1,3,5-triazine-2,4-diamine) is a chemical compound with the molecular formula C15H14N10. It is a diaminotriazine-based compound that is commonly used in the production of industrial products such as plastics, dyes, and pigments. This chemical is known for its high thermal stability and excellent UV resistance, making it a valuable component in the production of materials that require durability and longevity. Additionally, it is used as a curing agent in epoxy resins and as a crosslinking agent in the production of polymers. Due to its versatility and stability, 6,6'-(2,1-Phenylene)bis(1,3,5-triazine-2,4-diamine) is in high demand in various industrial applications.

Upstream product

• 127099-85-8 N-Cyanoguanidine 
• 91-15-6 phthalonitrile 

Relevant articles and documents

Green synthesis and self-association of 2,4-diamino-1,3,5-triazine derivatives

2,4-Diamino-1,3,5-triazines have been prepared by reaction of dicyandiamide with nitriles under microwave irradiation, a method that can be considered as a green procedure due to the reduction in the use of solvents during synthesis and purification, the short reaction time and the simplicity of the procedure. The structures have been confirmed in solution by NMR spectroscopy. Variable temperature experiments have been used to calculate the free energy of activation for rotation about the amino-triazine bond. The crystal structures of three 2,4-diamino-6-R-1,3,5-triazine derivatives (3a: R = phenyl, 3i: R = 1-piperidino and 3g: R = 1-phenylpyrazol-3-yl) have been determined by X-ray analysis. The N-H...N interactions change from structure to structure, resulting in a variation from pseudo-honeycomb networks to corrugated rosette layers.