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Usage

Uses

Used in Pharmaceutical Industry:
6-Benzyl-1,3,5-triazine-2,4-diamine is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex molecular structures, contributing to the development of new drugs with potential therapeutic benefits.
Used in Anticancer Research:
In the field of oncology, 6-Benzyl-1,3,5-triazine-2,4-diamine is studied for its potential as an anticancer agent, with research focusing on its ability to inhibit the growth of cancer cells and its potential synergistic effects when combined with other treatments.
Used in Materials Science:
6-Benzyl-1,3,5-triazine-2,4-diamine is utilized in the production of polymers and other industrial materials, where its unique chemical structure allows for the creation of novel materials with specific properties for various applications.
Used in Organic Synthesis:
As a key component in organic synthesis, 6-Benzyl-1,3,5-triazine-2,4-diamine is used as a building block for the creation of a wide range of organic compounds, showcasing its versatility and importance in chemical research and development.

Upstream product

• 140-29-4 phenylacetonitrile 
• 127099-85-8 N-Cyanoguanidine 
• 56-03-1 BIGUANIDE 
• 101-97-3 Ethyl 2-phenylethanoate 

Relevant academic research and scientific papers

Supramolecular hydrogen-bonded 1D arrangement in the crystals of 2,4-diamino-6-benzyl-1,3,5-triazine and 2,4-diamino-6-(4′-methylbenzyl)-1,3,5-triazine

Two crystals of triazine derivatives, 2,4-diamino-6-benzyl-1,3,5-triazine (1) and 2,4-diamino-6-(4′-methylbenzyl)-1,3,5-triazine (2), are synthesised by a direct reaction of cyanoguanidine with the respective cyanocompounds. The IR spectra of the compounds are very similar. In the crystals the molecules are interconnected by N{single bond}H?N hydrogen bonds forming one-dimensional hydrogen bonded polymer in 1 and three-dimensional hydrogen bonded network in 2. The arrangement of molecules in the crystal of 1 is denser than in 2 due to the π-π interactions between the π-clouds of the aromatic triazine rings that are absent in the crystal of 2. The geometries of the molecules in the crystals have been compared with those obtained by ab-initio molecular orbital calculated results that represent the geometries of molecules in the gas-phase.

Colorant compositions and processes

A process for making solid colored particles by preparing a reaction solution in water comprising formaldehyde, urea, a cyclic polyamine functional triazine compound, and acid. A dye can be incorporated into the reaction solution if a color other than white is desired. Particles are formed having an average particle size between 1 and 70 microns without the need to resort to crushing to break up agglomerates. Particles made by this process provide excellent color and are easily washable from a substrate when incorporated into a washable formulation. Additionally, it has been found that the incorporation of colored microcapsules of average size of 1-70 microns where the color is located primarily on or in the shell of the microcapsule also provides excellent washable compositions when incorporated into a washable formulation.