Poly(diallyldimethylammonium chloride(PDADMAC) - Mw 200,000-350,000 ,20 wt. % in water,250-500 cP(25 °C) , CAS No.26062-79-3

CAS: 26062-79-3 Cat. No.: P109720 Formula: (C₈H₁₆ClN)_n EC Number: 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

Overview

Product Description

Poly(diallyldimethylammonium chloride) solution (PDADMAC) is a cationic polyelectrolyte prepared by the radical polymerization of diallyldimethylammonium chloride (DADMAC) in presence of a catalyst in the form of an organic peroxide. It is widely utilized as a flocculant。

Product Application

PDADMAC can be used as an electrolytic solution in a variety of applications such as drug delivery, biomedical systems, and sensors, which include biosensors and chemical sensors.

Specifications

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

Specifications & Purity

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

Storage

Room temperature

Shipped In

Normal

Names and Identifiers

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

Isomeric SMILES

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

PubChem CID

33286

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: 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
• Description: 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

Chemical and Physical Properties

• Refractive Index: 1.375
• Flash Point(°C): >100°C
• Molecular Weight: 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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