937-35-9

Basic information

• Product Name: [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol
• Synonyms: [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol;hydroxymethylmelamine
• CAS NO: 937-35-9
• Molecular Formula: C₄H₈N₆O
• Molecular Weight: 156.14592
• EINECS: 213-327-0
• Mol File: 937-35-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 540.6°Cat760mmHg
• Flash Point: 280.8°C
• Appearance: /
• Density: 1.722g/cm³
• Vapor Pressure: 1.61E-12mmHg at 25°C
• Refractive Index: 1.839
• CAS DataBase Reference: [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol(937-35-9)
• EPA Substance Registry System: [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol(937-35-9)

Safety Data

• Hazardous Substances Data: 937-35-9(Hazardous Substances Data)

Usage

General Description

The chemical compound [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol, also known as aminomethanol or 4,6-diamino-1,3,5-triazin-2-ylamino-methanol, is an organic compound that contains a triazine ring structure. It is a derivative of triazine and contains both amino and alcohol functional groups. Aminomethanol has potential applications in the field of organic synthesis, pharmaceuticals, and materials science due to its unique structure and reactivity. Its properties and reactivity make it a valuable building block for the synthesis of various compounds and materials. Overall, aminomethanol has potential for various applications in the chemical and pharmaceutical industries due to its unique structure and reactivity.

InChI:InChI=1/C4H8N6O/c5-2-8-3(6)10-4(9-2)7-1-11/h11H,1H2,(H5,5,6,7,8,9,10)

Upstream product

• 50-00-0 formaldehyd 
• 108-78-1 2,4,6-triamino-s-triazine 
• 870-72-4 sodium formaldehyde bisulfite 

Downstream Products

• 5001-80-9 bis(hydroxymethyl)melamine 

Relevant articles and documents

Inorganic hybridized hydroxymethyl melamine phosphate and preparation method thereof

The invention belongs to the technical field of inorganic hybridized polymer materials and particularly relates to inorganic hybridized hydroxymethyl melamine phosphate and a preparation method thereof. The preparation method mainly includes steps: (1) hydroxymethylation reaction, to be more specific, adding melamine, formaldehyde and water into a reactor, and performing hydroxymethylation reaction under a weak-alkaline medium condition to obtain hydroxymethyl melamine; (2) hybridization reaction, to be more specific, reacting with inorganic hybrid compounds; (3) salt forming reaction; (4) cooling and filtering, to be more specific, cooling to 40DEG C or below, crystallizing and filtering to obtain the inorganic hybridized hydroxymethyl melamine phosphate. The inorganic hybridized hydroxymethyl melamine phosphate prepared according to the method has advantages that by hybridization cross-linking reaction with the inorganic hybrid compounds, high-temperature flame-retardant elements such as boron, molybdenum and stibium are added into hydroxymethyl melamine phosphate generated finally, and accordingly high temperature resistance and flame retardation of the hydroxymethyl melamine phosphate are improved.

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.