Tetrahexylammonium bromide - for ion pair chromatography, ≥99% , CAS No.4328-13-6

CAS: 4328-13-6 Cat. No.: T120735 Peso molecular: 434.58 Beilstein Registry Number: 3637302 Número EC: 224-363-1

GRADE & PURITY for Ion pair chromatography, ≥99%

Synonyms

DTXSID50884059 | AKOS015833006 | tetrahexylazanium bromide | D70474 | 1-Hexanaminium, N,N,N-trihexyl-, bromide | C24H52BrN | 1-Hexanaminium, N,N,N-trihexyl-, bromide (1:1) | AS-58722 | SCHEMBL82322 | Tetrahexylammonium bromide | EINECS 224-363-1 | HY-W010

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Descripción general

Tetrahexylammonium bromide can be used:

· As a hydrogen bond acceptor in the preparation of deep eutectic solvents which can be used for desulfurization and denitrogenation from n-heptane.

· To produce aqueous biphasic system for the heavy metal ions preconcentration.

· As a phase transfer salt to fabricate an optical chemical gas-sensor.

Specifications

Sinónimos

DTXSID50884059 | AKOS015833006 | tetrahexylazanium bromide | D70474 | 1-Hexanaminium, N, N, N-trihexyl-, bromide | C24H52BrN | 1-Hexanaminium, N, N, N-trihexyl-, bromide (1:1) | AS-58722 | SCHEMBL82322 | Tetrahexylammonium bromide | EINECS 224-363-1 | HY-W010

Especificaciones y pureza

for ion pair chromatography, ≥99%

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged, Desiccated

Enviado en

Normal

Grado

for Ion pair chromatography

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 504755238
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504755238
• Sonrisas canónicas: CCCCCC[N+](CCCCCC)(CCCCCC)CCCCCC.[Br-]
• IUPAC Name: tetrahexylazanium;bromide
• InChIKey: SYZCZDCAEVUSPM-UHFFFAOYSA-M
• INCHI: 1S/C24H52N.BrH/c1-5-9-13-17-21-25(22-18-14-10-6-2,23-19-15-11-7-3)24-20-16-12-8-4;/h5-24H2,1-4H3;1H/q+1;/p-1
• Isómeros SMILES: CCCCCC[N+](CCCCCC)(CCCCCC)CCCCCC.[Br-]
• WGK Alemania: 3
• CAS alternativo: 20256-54-6
• Peso molecular: 434.58
• Beilstein: 3637302

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 bromide salts Hydrocarbon derivatives Amines
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetraalkylammonium salt - Organopnictogen compound - Hydrocarbon derivative - Organic bromide 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

• Sensibilidad: Moisture sensitive
• Punto de fusión (°C): 98-100°C
• Peso molecular: 434.600 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 20
• Exact Mass: 433.328 Da
• Monoisotopic Mass: 433.328 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 26
• Formal Charge: 0
• Complexity: 195.000
• 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. Min Wang, Yajie Yue, Xiaoning Wei, Jinyuan Zhang, Xinyuan Bi, Liyan Jia, Xu Jing.  (2024)  Chitosan-based emulsive liquid-liquid microextraction for the determination of strobilurin fungicides in water samples.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39486720] [10.1016/j.ijbiomac.2024.137136]

2. Binwang Yang, Zhixiong Ye, Feiyu Lu, Jianna Yu, Jiaxu Liu, Xiuqing Zheng, Cheng Wang, Lian Duan, Zhijian Yang, Guoxing Jing, Wen Liu, Wenshan Li, Wenjie Liu.  (2024)  High Resolving Power Electrospray Ionization Ion Mobility Spectrometer Based on Fourier Deconvolution Multiplexing.  ANALYTICAL CHEMISTRY,      [PMID:39413295] [10.1021/acs.analchem.4c04549]

3. Xiao-Ya Wang, Wen-Qiang Gong, Fei-Feng Mao, Wei Hui, Xian-Lu Wu, Tiao Zhang, Yan Zhou, Jia-Yin Zhang, Duan-Jian Tao.  (2026)  Ultrahigh SO2 selective absorption in SO2/CO2 mixtures via reversible solid–liquid phase transition in tunable ionic liquids.  CHEMICAL ENGINEERING SCIENCE,      [PMID:] [10.1016/j.ces.2026.123635]