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Triazine

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Triazine 

any of several six-membered heterocyclic compounds containing three nitrogen atoms in the ring. The substituted triazines, which are the best known, exist in all three possible systems: vicinal 1,2,3-triazines (I), asymmetric 1,2,4-triazines (II), and symmetric 1,3,5-triazines (III).

Triazines are strong bases, which yield salts with acids. Substituted 1,3,5-triazines, which are used as herbicides (for example, atrazine, desmetryn, and prometryn) and dyes and in the production of plastics and rubbers, have the greatest practical importance. They are obtained, for example, from cyanuric chloride (1) or by the trimerization of the nitriles of carboxylic acids (2):



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CSIRO Entomology's Cameron Begley says the enzyme also works well against a range of other triazine herbicides and, once in commercial production, would benefit farmers and water consumers wherever triazines are used.
Triazine chemistry also added another facet to stabilization from UV light by providing significant improvements in durability.
The crosslinking agent has a glass transition temperature of at least 10[degrees]C and is substantially free of functional groups that are reactive with the aminoplast resin; wherein the aminoplast resin comprises an aminotriazine compound comprising an (alkoxyalkyl) aminotriazine having one or less non-alkylated NH bond per triazine ring.
 
 
 
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