5606-23-5

Basic information

• Product Name: ETHYLMELAMINE
• Synonyms: ETHYLMELAMINE
• CAS NO: 5606-23-5
• Molecular Formula: C5H10 N6
• Molecular Weight: 154.17
• Mol File: 5606-23-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 436.8°Cat760mmHg
• Flash Point: 218°C
• Appearance: /
• Density: 1.406g/cm³
• Vapor Pressure: 7.86E-08mmHg at 25°C
• Refractive Index: 1.718
• CAS DataBase Reference: ETHYLMELAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYLMELAMINE(5606-23-5)
• EPA Substance Registry System: ETHYLMELAMINE(5606-23-5)

Safety Data

• Hazardous Substances Data: 5606-23-5(Hazardous Substances Data)

Usage

General Description

Ethylmelamine is a chemical compound that is primarily used as an intermediate in the production of pharmaceuticals, pesticides, and industrial chemicals. It is a colorless liquid with a strong odor, and it is soluble in water and organic solvents. Ethylmelamine is a versatile compound that can undergo various reactions to produce a wide range of products. It is commonly used as a cross-linking agent in the production of resins and polymers, as a precursor for the synthesis of dyes and pigments, and as a starting material for the production of other nitrogen-based compounds. While ethylmelamine itself has limited direct applications, its derivates and reactions products are widely used in various industries.

InChI:InChI=1/C5H10N6/c1-2-8-5-10-3(6)9-4(7)11-5/h2H2,1H3,(H5,6,7,8,9,10,11)

Upstream product

• 3397-62-4 2-Chloro-4,6-diamino-1,3,5-triazine 
• 75-04-7 ethylamine 
• 123-91-1 1,4-dioxane 

Relevant articles and documents

Method for modifying 1,3,5-triazine derivatives

PCT No. PCT/JP96/03762 Sec. 371 Date Jun. 22, 1998 Sec. 102(e) Date Jun. 22, 1998 PCT Filed Dec. 24, 1996 PCT Pub. No. WO97/24338 PCT Pub. Date Jul. 10, 1997A method for modifying 1,3,5-triazine derivatives characterized by heating and reacting a 1,3,5-triazine derivatives having at least one amino or mono-substituted amino group on a carbon atom or atoms on its ring with an alcohol in the presence of a metal catalyst and a hydrogen atom to introduce an alkyl group or an alkenyl group into each amino or mono-substituted amino group; another method for modifying 1,3,5-triazine derivatives characterized by heating and reacting a 1,3,5-triazine derivatives having at least one amino or mono-substituted amino group on a carbon atom or atoms on its ring with a dihydric alcohol in the presence of a metal catalyst and a hydrogen atom to introduce an alkyl group having a hydroxyl group into each amino or mono-substituted amino group; and 1,3,5-triazine derivatives obtained by the methods. The various modified sustituted 1,3,5-triazine derivatives thus produced are generally obtained as a mixture. These derivatives can be isolated as compounds having high-purity by a normal separation method for organic compounds, and the compounds are usable in the various applications mentioned in the specification.