Dodecylethyldimethylammonium bromide - ≥99% , CAS No.68207-00-1

CAS: 68207-00-1 Cat. No.: D113032 Peso molecular: 322.37 Beilstein Registry Number: 6007021 Número EC: 269-249-2

GRADE & PURITY ≥99%

Synonyms

EDDAB | 1-Dodecanaminium, N-ethyl-N,N-dimethyl-, bromide | N-Ethyl-N,N-dimethyldodecan-1-aminium bromide | N-Dodecyl-N,N-dimethyl-N-ethylammonium bromide | Q27274290 | DODECYL-N,N-DIMETHYL-N-ETHYLAMMONIUM BROMIDE | MFCD00043170 | B2YOU5667H | DODECYL(ETHY

Storage

Room temperature,Desiccated

Shipped In

Normal

Descripción general

Application：

Dodecylethyldimethylammonium bromide (C12EDMAB) can be used:

As a growth-directing surfactant in the synthesis of monodisperse gold nanorods.

As a surfactant in the synthesis of poly(methyl methacrylate)-poly(N-isopropylacrylamide) core-shell particles via emulsion polymerization.

As an additive in the synthesis of mesoporous nanocrystalline TiO2 microspheres to increasing the degree of crystallization and modification in the texture of TiO2.

Specifications

Sinónimos

EDDAB | 1-Dodecanaminium, N-ethyl-N, N-dimethyl-, bromide | N-Ethyl-N, N-dimethyldodecan-1-aminium bromide | N-Dodecyl-N, N-dimethyl-N-ethylammonium bromide | Q27274290 | DODECYL-N, N-DIMETHYL-N-ETHYLAMMONIUM BROMIDE | MFCD00043170 | B2YOU5667H | DODECYL(ETHY

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Room temperature, Desiccated

Enviado en

Normal

Pureza

≥99%

Nombres e identificadores

• Sonrisas canónicas: CCCCCCCCCCCC[N+](C)(C)CC.[Br-]
• IUPAC Name: dodecyl-ethyl-dimethylazanium;bromide
• InChIKey: FFGSPQDSOUPWGY-UHFFFAOYSA-M
• INCHI: 1S/C16H36N.BrH/c1-5-7-8-9-10-11-12-13-14-15-16-17(3,4)6-2;/h5-16H2,1-4H3;1H/q+1;/p-1
• Isómeros SMILES: CCCCCCCCCCCC[N+](C)(C)CC.[Br-]
• WGK Alemania: 3
• Peso molecular: 322.37
• Beilstein: 6007021
• Reaxy-Rn: 6007021
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6007021&ln=

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: Organic bromide salts Hydrocarbon derivatives Amines Organic cations
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetraalkylammonium salt - Hydrocarbon derivative - Organic bromide salt - Organic salt - Amine - Organic cation - 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

Objetivos asociados (humanos)

DNM1 Tbio Dynamin-1 (215 Activities)

Discover Target: DNM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive
• Punto de fusión (°C): 185-188°C
• Peso molecular: 322.370 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 12
• Exact Mass: 321.203 Da
• Monoisotopic Mass: 321.203 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 152.000
• 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: 2

XLogP3

Referencias

1. Haofei Li, Zhuojun Cai, Yilin Wang.  (2020)  Impact Behaviors on Superhydrophobic Surfaces for Water Droplets of Asymmetric Double-Chain Quaternary Ammonium Surfactants.  LANGMUIR,      [PMID:33166156] [10.1021/acs.langmuir.0c02783]

2. Jinghui Wang, Renliang Huang, Wei Qi, Rongxin Su, Zhimin He.  (2017)  Oriented Enzyme Immobilization at the Oil/Water Interface Enhances Catalytic Activity and Recyclability in a Pickering Emulsion.  LANGMUIR,      [PMID:28968113] [10.1021/acs.langmuir.7b02862]