5606-16-6

Basic information

• Product Name: 2-AMINO-4,6-BIS(ETHYLAMINO)-1,3,5-TRIAZINE
• Synonyms: N2,N4-Diethylmelamine
• CAS NO: 5606-16-6
• Molecular Formula: C₇H₁₄N₆
• Molecular Weight: 182.23
• Mol File: 5606-16-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 392.8°Cat760mmHg
• Flash Point: 191.4°C
• Appearance: /
• Density: 1.271g/cm³
• Vapor Pressure: 2.23E-06mmHg at 25°C
• Refractive Index: 1.665
• PKA: 5.86±0.10(Predicted)
• CAS DataBase Reference: 2-AMINO-4,6-BIS(ETHYLAMINO)-1,3,5-TRIAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-4,6-BIS(ETHYLAMINO)-1,3,5-TRIAZINE(5606-16-6)
• EPA Substance Registry System: 2-AMINO-4,6-BIS(ETHYLAMINO)-1,3,5-TRIAZINE(5606-16-6)

Safety Data

• Hazardous Substances Data: 5606-16-6(Hazardous Substances Data)

Usage

Physical State

White crystalline solid

Uses

Production of plastics
Adhesives
Flame retardants
Fertilizers

Metabolite

of the pesticide cyromazine

Safety Concerns

Subject of product recalls and bans
Presence in food and milk products
Health risks include kidney and bladder stones, kidney damage, urinary tract infections

Continued Use

Despite safety concerns, due to advantageous properties

InChI:InChI=1/C7H14N6/c1-3-9-6-11-5(8)12-7(13-6)10-4-2/h3-4H2,1-2H3,(H4,8,9,10,11,12,13)

Upstream product

• 74-96-4 ethyl bromide 

Downstream Products

• 7664-41-7 ammonia 
• 75-04-7 ethylamine 
• 108-80-5 isocyanuric acid 

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.