2,4,6-Tris[bis(methoxymethyl)amino]-1,3,5-triazine - ≥98%(HPLC) , CAS No.3089-11-0

CAS: 3089-11-0 Cat. No.: T162539 Peso molecular: 390.44 Beilstein Registry Number: 26(3/4)1274 Número EC: 221-422-3 PubChem CID: 62479

GRADE & PURITY ≥98%(HPLC)

Synonyms

T2059 | Hexa(methoxymethyl)melamine | HEXAKIS(METHOXYMETHYL)MELAMINE | N,N,N',N',N'',N''-Hexakis(methoxymethyl)-1,3,5-triazine-2,4,6-triamine | SB73698 | hexamethoxymethylmelamine (HMMM) | Hexamethylol-melamin-hexa-methylaether | W-109858 | Methazin | Mal

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

T2059 | Hexa(methoxymethyl)melamine | HEXAKIS(METHOXYMETHYL)MELAMINE | N, N, N', N', N'', N''-Hexakis(methoxymethyl)-1, 3, 5-triazine-2, 4, 6-triamine | SB73698 | hexamethoxymethylmelamine (HMMM) | Hexamethylol-melamin-hexa-methylaether | W-109858 | Methazin | Mal

Especificaciones y pureza

≥98%(HPLC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%(HPLC)

Nombres e identificadores

• Pubchem Sid: 488183582
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488183582
• Sonrisas canónicas: COCN(COC)C1=NC(=NC(=N1)N(COC)COC)N(COC)COC
• IUPAC Name: 2-N,2-N,4-N,4-N,6-N,6-N-hexakis(methoxymethyl)-1,3,5-triazine-2,4,6-triamine
• InChIKey: BNCADMBVWNPPIZ-UHFFFAOYSA-N
• INCHI: 1S/C15H30N6O6/c1-22-7-19(8-23-2)13-16-14(20(9-24-3)10-25-4)18-15(17-13)21(11-26-5)12-27-6/h7-12H2,1-6H3
• Isómeros SMILES: COCN(COC)C1=NC(=NC(=N1)N(COC)COC)N(COC)COC
• RTECS: XZ1065000
• PubChem CID: 62479
• Peso molecular: 390.44
• Beilstein: 26(3/4)1274
• Reaxy-Rn: 356813

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Amines
        • Level5 Tertiary amines
          • Level6 Tertiary alkylarylamines
            • Level7 Dialkylarylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Tertiary amines - Tertiary alkylarylamines
• Direct Parent: Dialkylarylamines
• Alternative Parents: N-aliphatic s-triazines 1,3,5-triazines Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Dialkylarylamine - N-aliphatic s-triazine - Amino-1,3,5-triazine - 1,3,5-triazine - Triazine - Heteroaromatic compound - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as dialkylarylamines. These are aliphatic aromatic amines in which the amino group is linked to two aliphatic chains and one aromatic group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Solubilidad: Soluble in water
• Punto de fusión (°C): 52℃
• Peso molecular: 390.440 g/mol
• XLogP3: 1.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 12
• Rotatable Bond Count: 15
• Exact Mass: 390.223 Da
• Monoisotopic Mass: 390.223 Da
• Topological Polar Surface Area: 104.000 Ų
• Heavy Atom Count: 27
• Formal Charge: 0
• Complexity: 289.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Xun Luo, Wenyan Lv, Hongyu Luo, Lier Wang, Pan Liu, Xin Deng, Zhiping Liu, Renbo Wei, Zhiyuan Xiong, Bo Tang.  (2025)  Mass-produced anti-fogging films with excellent performances formed from amphiphilic random copolymers via roll-to-roll coating.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2025.109089]