4039-98-9

Usage

Uses

Used in Plastics and Adhesives Industry:
N,N-dimethyl-1,3,5-triazine-2,4-diamine is used as a key component in the production of plastics and adhesives for its ability to enhance the durability and heat resistance of these materials.
Used in Flame Retardants:
In the flame retardants industry, N,N-dimethyl-1,3,5-triazine-2,4-diamine is utilized as an effective additive to reduce the flammability of various materials, thereby improving their fire safety.
Used in Dinnerware and Kitchenware Manufacturing:
N,N-dimethyl-1,3,5-triazine-2,4-diamine is used as a raw material in the manufacturing of durable and heat-resistant dinnerware and kitchenware, providing consumers with long-lasting and high-quality products.
Used as a Nitrogen-Rich Fertilizer:
In agriculture, N,N-dimethyl-1,3,5-triazine-2,4-diamine serves as a nitrogen-rich fertilizer, promoting plant growth and enhancing crop yields.
However, it is crucial to note that melamine has been associated with health risks and controversies, particularly due to its presence in some food products. In high doses, it can cause kidney damage and failure in humans and animals. Therefore, proper handling, regulation, and caution are essential when using N,N-dimethyl-1,3,5-triazine-2,4-diamine in consumer products to ensure safety and prevent adverse health effects.

InChI:InChI=1/C5H9N5/c1-10(2)5-8-3-7-4(6)9-5/h3H,1-2H3,(H2,6,7,8,9)

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Relevant academic research and scientific papers

Metal free [4+1] and [5+1] annulation reactions to prepare heterocycles using DMF and its derivatives as one-carbon source

1,2,4-Triazolo[3,4-a]pyridines and related heterocycles and substituted triazines were commonly discovered scaffolds in a variety of pharmaceutical and agrochemical agents. Herein, we report a highly efficient and practical method using DMF and its derivative for the [4+1] and [5+1] annulation reactions to prepare these heterocycles. This metal free reaction takes advantages of shelf stable DMF as solvent and carbon donor, imidazole chloride as a catalyst, the mild reaction condition tolerates a broad substrate range and substitutes. The prepared 3-unsubstituted 1,2,4-triazolo[3,4-a]pyridine and derivatives allow further introduction of a variety of functional group1 at 3-position.

Imidazole-triazine type compound and preparation method and application thereof

The invention provides an imidazole-triazine type compound which is shown as the formula 3 in the description and a preparation method and application thereof. The method comprises the steps that a triazine compound and an alpha,beta-unsaturated ketone type compound are mixed and added into a solvent, under the existence of a metal copper catalyst and an oxidizing material, the mixed solution is stirred and reacts 5-20 hours under the temperature of 60-150 DEG C, after the reaction is finished, the reacted solution is subjected to post processing, and the imidazole-triazine type compound which is shown as the formula 3 is obtained; the metal copper catalyst is halogenide of the copper or a copper salt; the oxidizing material is a halogen elementary substance. The imidazole-triazine type compound can be applied to prepare antibacterial drugs or antibacterial agents, and the preferred antibacterial drugs are the drugs which inhibit activity of escherichia coli.

2,4-diamine-1,3,5-triazine compound, preparation method and application thereof

The invention provides a 2,4-diamine-1,3,5-triazine compound represented as the formula (III). A preparation method includes the following steps: adding compounds represented as the formulas (I) and (II), a metal copper catalyst, a ligand, an alkaline sub

Diuretics on the basis of N substituted 2,4 diamino s triazines by cyclisation of biguanides

The structural class of 2,4 diamino s triazines (5) functioning as diuretics has become accessible by a novel preparatory procedure. The new synthesis is based on the aminomethinylating principle of s triazine (1), under the action of which biguanides (2) are cyclized to 5 passing through the intermediary states 3 and 4.