Poli(cloruro de dialildimetilamonio（PDADMAC） - Mw 200.000-350.000 ,20 % en peso en agua,250-500 cP(25 °C) , CAS No.26062-79-3

CAS: 26062-79-3 Cat. No.: P109720 Fórmula: (C₈H₁₆ClN)_n Número EC: 607-855-4 PubChem CID: 33286

GRADE & PURITY Mw 200,000-350,000 ,20 wt. % in water,250-500 cP(25 °C)

Synonyms

N,N-dimethyldiallylammonium chloride | Diallyldimethylammonium chloride | DTXCID407650 | NSC59284 | NSC-59284 | 2-Propen-1-aminium,N-dimethyl-N-2-propenyl-, chloride | Agefloc WT 20 | NCGC00257309-01 | Merquat 100 | 2-Propen-1-aminium, N,N-dimethyl-N-2-pr

Storage

Room temperature

Shipped In

Normal

Descripción general

Descripción del producto

La solución de poli(cloruro de dialildimetilamonio) (PDADMAC) es un polielectrolito catiónico preparado por polimerización radical de cloruro de dialildimetilamonio (DADMAC) en presencia de un catalizador en forma de peróxido orgánico. Se utiliza ampliamente como floculante。

Aplicación del producto

El PDADMAC puede utilizarse como solución electrolítica en diversas aplicaciones, como la administración de fármacos, los sistemas biomédicos y los sensores, que incluyen biosensores y sensores químicos.

Specifications

Sinónimos

N,N-dimethyldiallylammonium chloride | Diallyldimethylammonium chloride | DTXCID407650 | NSC59284 | NSC-59284 | 2-Propen-1-aminium,N-dimethyl-N-2-propenyl-, chloride | Agefloc WT 20 | NCGC00257309-01 | Merquat 100 | 2-Propen-1-aminium, N,N-dimethyl-N-2-pr

Especificaciones y pureza

Mw 200.000-350.000 ,20 % en peso en agua,250-500 cP(25 °C)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Nombres e identificadores

Pubchem Sid

508816155

IUPAC Name

dimethyl-bis(prop-2-enyl)azanium;chloride

InChIKey

GQOKIYDTHHZSCJ-UHFFFAOYSA-M

INCHI

1S/C8H16N.ClH/c1-5-7-9(3,4)8-6-2;/h5-6H,1-2,7-8H2,3-4H3;1H/q+1;/p-1

Isómeros SMILES

C[N+](C)(CC=C)CC=C.[Cl-]

PubChem CID

33286

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Quaternary ammonium salts

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Quaternary ammonium salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetraalkylammonium salts
• Alternative Parents: Organopnictogen compounds Organic chloride salts Hydrocarbon derivatives Amines
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetraalkylammonium salt - Organopnictogen compound - Hydrocarbon derivative - Organic chloride salt - Organic salt - Amine - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as tetraalkylammonium salts. These are organonitrogen compounds containing a quaternary ammonium substituted with four alkyl chains.
• 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: 1.375
• Punto de inflamación (°C): >100°C
• Peso molecular: 161.670 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 161.097 Da
• Monoisotopic Mass: 161.097 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 91.100
• 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

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