38228-21-6

Basic information

• Product Name: [(6-amino-1,3,5-triazine-2,4-diyl)dinitrilo]tetrakismethanol
• Synonyms: [(6-amino-1,3,5-triazine-2,4-diyl)dinitrilo]tetrakismethanol;2-Amino-4,6-bis[bis(hydroxymethyl)amino]-1,3,5-triazine
• CAS NO: 38228-21-6
• Molecular Formula: C₇H₁₄N₆O₄
• Molecular Weight: 246.22386
• EINECS: 253-839-1
• Mol File: 38228-21-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 620.1°Cat760mmHg
• Flash Point: 328.8°C
• Appearance: /
• Density: 1.792g/cm³
• Vapor Pressure: 3.09E-16mmHg at 25°C
• Refractive Index: 1.814
• CAS DataBase Reference: [(6-amino-1,3,5-triazine-2,4-diyl)dinitrilo]tetrakismethanol(CAS DataBase Reference)
• NIST Chemistry Reference: [(6-amino-1,3,5-triazine-2,4-diyl)dinitrilo]tetrakismethanol(38228-21-6)
• EPA Substance Registry System: [(6-amino-1,3,5-triazine-2,4-diyl)dinitrilo]tetrakismethanol(38228-21-6)

Safety Data

• Hazardous Substances Data: 38228-21-6(Hazardous Substances Data)

Usage

General Description

[(6-amino-1,3,5-triazine-2,4-diyl)dinitrilo]tetrakismethanol is a chemical compound with the molecular formula C8H12N6O4. It is a complex organic molecule that contains a central 1,3,5-triazine ring with amino and nitro functional groups attached to it. The compound also contains four methanol (CH3OH) groups attached to the central triazine ring. This chemical may have various potential applications in fields such as organic synthesis, pharmaceuticals, and materials science due to its unique molecular structure and potential reactivity. Further research and testing would be needed to fully understand its properties and potential applications.

InChI:InChI=1/C7H14N6O4/c8-5-9-6(12(1-14)2-15)11-7(10-5)13(3-16)4-17/h14-17H,1-4H2,(H2,8,9,10,11)

Upstream product

• 50-00-0 formaldehyd 
• 108-78-1 2,4,6-triamino-s-triazine 

Relevant articles and documents

Canonical Chemical Theories Exemplified by the Mehtylolation of Urea and Melamine

Old and recent data on equilibria and kinetics of methylolation of urea and melamine are analysed.The theoretical framework affords a sequence, claimed to be canonical of successive phenomenological approximations.The theory, expounded earlier, begin with two successive schemes whose essentials go back to early work by Pauling and by Flory.The two stages here suffice to show that all the data from eight laboratories, covering the six-membered family of methylol ureas and rhe ten-membered family of methylol melamines, are in quantitative agreement, a circumstance unsespected by other workers in the field.The statisticalthermodynamic and kinetic principles involved are therefore expounded in more detail than before.Using them, very small substituent effects (e.g O.35 kJ kol-1 are deduced with high significance and accuracy.Owing largly to the recent measurement by Tomita, the methylol melamines are claimed currently to be the thermdinamically best characterised family in the chemical literature.A challenge arises for theoretical chemists to test quantum-theoreticaltechniques against the measured energetics of substituent effects in this family, and to exploit for other families the graph-theoretical analysis of molecular additivity which underlies the approximation schemes, which already well tested.