Poly(melamine-co-formaldehyde) methylated, solution - average Mₙ ~432, 84wt. % in 1-butanol , CAS No.68002-20-0

CAS: 68002-20-0 Cat. No.: P466386 Número EC: 614-203-2 PubChem CID: 93374

GRADE & PURITY average Mₙ ~432, 84wt. % in 1-butanol

Synonyms

melamine/formaldehyde | MELAMINE FORMALDEHYDE | melamine-formaldehyde | melamine formalin | Melamine, formaldehyde, butanol resin | DTXSID10974980 | formaldehyde melamine | IVJISJACKSSFGE-UHFFFAOYSA-N | SCHEMBL20816 | Cymel 481 resin | Formaldehyde--1,3,5

Storage

Room temperature

Descripción general

Poly(melamine-co-formaldehyde) methylated, solution (PMF) is a heat initiated cross-linking agent that forms an optically transparent solution. It can be linked with poly(4-vinly phenol) (PVP) by attaching with phenol groups that reduce the hydroxyl units in the blend.PMF can be used in the preparation of PVP-based ink, which can be used in inkjet printing for the development of electronic components such as:organic thin film transistorradio frequency capacitorsparallel plate capacitorsmetal insulated metal (MIM) capacitor

Specifications

Sinónimos

melamine/formaldehyde | MELAMINE FORMALDEHYDE | melamine-formaldehyde | melamine formalin | Melamine, formaldehyde, butanol resin | DTXSID10974980 | formaldehyde melamine | IVJISJACKSSFGE-UHFFFAOYSA-N | SCHEMBL20816 | Cymel 481 resin | Formaldehyde--1, 3, 5

Especificaciones y pureza

average Mₙ ~432, 84wt. % in 1-butanol

Condiciones de almacenamiento de almacenamiento

Room temperature

Nombres e identificadores

• Sonrisas canónicas: C=O.C1(=NC(=NC(=N1)N)N)N
• IUPAC Name: formaldehyde;1,3,5-triazine-2,4,6-triamine
• InChIKey: IVJISJACKSSFGE-UHFFFAOYSA-N
• INCHI: 1S/C3H6N6.CH2O/c4-1-7-2(5)9-3(6)8-1;1-2/h(H6,4,5,6,7,8,9);1H2
• Isómeros SMILES: C=O.C1(=NC(=NC(=N1)N)N)N
• PubChem CID: 93374
• Número ONU: 1866C

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Carbonyl compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Not available
• Direct Parent: Carbonyl compounds
• Alternative Parents: Organic oxides Hydrocarbon derivatives
• Molecular Framework: Not available
• Substituents: Organic oxide - Hydrocarbon derivative - Carbonyl group - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as carbonyl compounds. These are organic compounds containing a carbonyl group, with the general structure RC(=O)R', where R=organyl, R'=H, N, O, organyl group or halide 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

• Índice de refracción: n20/D 1.515
• Punto de inflamación (°F): Not applicable
• Punto de inflamación (°C): Not applicable
• Punto de ebullición (°C): 118℃
• Peso molecular: 156.150 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 0
• Exact Mass: 156.076 Da
• Monoisotopic Mass: 156.076 Da
• Topological Polar Surface Area: 134.000 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 65.300
• 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: 2

XLogP3

Referencias

1. Chunzu Cheng, Zhongkai Xu, Qingbo Zhao, Min Gao, Ting Li, Guozhen Li, Kedong Chi, Jigang Xu, Bowen Cheng.  (2024)  Prepartion of low-cost blended lyocell fibres with phosphorus, nitrogen, halogen and inorganic flame retardants and study on their synergistic fame retardancy mechanism.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39471917] [10.1016/j.ijbiomac.2024.136971]