5425-82-1

Basic information

• Product Name: 2-Chloro-4-methylamino-6-amino-1,3,5-triazine-
• Synonyms: 2-Chloro-4-methylamino-6-amino-1,3,5-triazine-
• CAS NO: 5425-82-1
• Molecular Formula: C4H6ClN5
• Molecular Weight: 159.58
• Mol File: 5425-82-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 401.2°Cat760mmHg
• Flash Point: 196.5°C
• Appearance: /
• Density: 1.552g/cm³
• Vapor Pressure: 1.2E-06mmHg at 25°C
• Refractive Index: 1.689
• CAS DataBase Reference: 2-Chloro-4-methylamino-6-amino-1,3,5-triazine-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Chloro-4-methylamino-6-amino-1,3,5-triazine-(5425-82-1)
• EPA Substance Registry System: 2-Chloro-4-methylamino-6-amino-1,3,5-triazine-(5425-82-1)

Safety Data

• Hazardous Substances Data: 5425-82-1(Hazardous Substances Data)

Usage

General Description

2-Chloro-4-methylamino-6-amino-1,3,5-triazine, also known as Atrazine, is a herbicide commonly used in agriculture to control broadleaf and grassy weeds. It acts by inhibiting photosynthesis in target plants, leading to their eventual death. Atrazine is a chlorotriazine compound and is classified as a restricted use pesticide due to its potential environmental and human health impacts. It has been found to persist in soil and water, posing a risk of contamination to aquatic ecosystems and drinking water sources. The compound has also been linked to adverse effects on wildlife and human health, including developmental and reproductive toxicity. Due to these concerns, the use of atrazine has been banned or heavily restricted in several countries.

InChI:InChI=1/C4H6ClN5/c1-7-4-9-2(5)8-3(6)10-4/h1H3,(H3,6,7,8,9,10)

Upstream product

• 933-20-0 4,6-dichloro-1,3,5-triazin-2-amine 
• 74-89-5 methylamine 
• 593-51-1 methylamine hydrochloride 
• 27282-80-0 4,6-dichloro-N-methyl-1,3,5-triazin-2-amine 

Downstream Products

• 37019-25-3 6-methoxy-N-methyl-[1,3,5]triazine-2,4-diamine 
• 16268-82-9 N²,N²,N⁴-trimethylmelamine 

Relevant articles and documents

Microwave assisted synthesis, docking and antimalarial evaluation of hybrid PABA-substituted 1,3,5-triazine derivatives

A series of novel PABA-substituted 1,3,5-triazine derivatives were developed via microwave assisted synthesis and subsequently tested for antimalarial activity against chloroquine sensitive 3D7 strain of Plasmodium falciparum using chloroquine as standard. Antimalarial screening result showed that synthesized compounds exhibited IC50 in the range of 4.46 to 79.72 μg mL?1. Among the tested compounds, 4c and 4f showed significant antimalarial activity with low binding energies (BE) -172.32 and 160.41 kcal mol?1 via interacting with Arg122 through the involvement of COOH of the phenyl linked to 1,3,5-triazine. In conclusion, these core scaffolds can be used for future antimalarial drug development.

N-ALKYL MELAMINE FORMALDEHYDE CROSS-LINKING AND CURABLE COMPOSITIONS

This invention relates to bis-N-alkyl melamine formaldehyde cross-linking composition or a mixture of bis- and tris-N-alkyl melamine formaldehyde cross-linking composition. This invention also contemplates curable compositions comprising the bis-N-alkyl melamine formaldehyde composition and an active hydrogen-containing material. The invention further encompasses a curable composition comprising a mixture of bis- and tris-N-alkyl melamine formaldehyde compounds and an active hydrogen-containing material.

Herbicidal sulfonamides

Herbicidal sulfonamides such as 2-[[[4-(methylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-yl]aminocarbonyl]aminosulfonyl]benzoic acid, methyl ester are useful as herbicides and plant growth regulants.