Sulfato ácido de tetraetilamonio - ≥99% , CAS No.16873-13-5

CAS: 16873-13-5 Cat. No.: T113710 Peso molecular: 227.32 Beilstein Registry Number: 6590581 Número EC: 240-899-9 PubChem CID: 167582

GRADE & PURITY ≥99%

Synonyms

J-010480 | T3506 | tetraethylazanium hydrogen sulfate | FT-0659633 | hydrogen sulfate;tetraethylazanium | AKOS015915196 | 3-PYRROLIDIN-1-YLACRYLICACIDMETHYLESTER | EINECS 240-899-9 | AS-69274 | DTXSID10168605 | Ethanaminium, N,N,N-triethyl-, hydrogen sulf

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

El hidrogenosulfato de tetraetilamonio es un reactivo de cromatografía de pares de iones (IPC) adecuado para la separación aniónica clasificada por la longitud de la cadena de carbono.
El hidrogenosulfato de tetraetilamonio puede utilizarse como reactivo de par iónico para el análisis de tensioactivos alifáticos y aromáticos sulfonados en lodos de depuradora mediante extracción por par iónico/fluido supercrítico y cromatografía de gases/espectrometría de masas de derivación.

Specifications

Sinónimos

J-010480 | T3506 | tetraethylazanium hydrogen sulfate | FT-0659633 | hydrogen sulfate;tetraethylazanium | AKOS015915196 | 3-PYRROLIDIN-1-YLACRYLICACIDMETHYLESTER | EINECS 240-899-9 | AS-69274 | DTXSID10168605 | Ethanaminium, N, N, N-triethyl-, hydrogen sulf

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 488188412
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488188412
• Sonrisas canónicas: CC[N+](CC)(CC)CC.OS(=O)(=O)[O-]
• IUPAC Name: hydrogen sulfate;tetraethylazanium
• InChIKey: CREVBWLEPKAZBH-UHFFFAOYSA-M
• INCHI: 1S/C8H20N.H2O4S/c1-5-9(6-2,7-3)8-4;1-5(2,3)4/h5-8H2,1-4H3;(H2,1,2,3,4)/q+1;/p-1
• Isómeros SMILES: CC[N+](CC)(CC)CC.OS(=O)(=O)[O-]
• WGK Alemania: 3
• PubChem CID: 167582
• Peso molecular: 227.32
• Beilstein: 6590581

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Organic sulfuric acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Organic sulfuric acids and derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic sulfuric acids and derivatives
• Alternative Parents: Tetraalkylammonium salts Organopnictogen compounds Organic salts Organic oxides Hydrocarbon derivatives Amines
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetraalkylammonium salt - Quaternary ammonium salt - Organic sulfuric acid or derivatives - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organonitrogen compound - Amine - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as organic sulfuric acids and derivatives. These are organic compounds containing the sulfuric acid or a derivative thereof.
• 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

• Solubilidad: Soluble in water
• Sensibilidad: Hygroscopic
• Punto de fusión (°C): 243-245°C
• Peso molecular: 227.320 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 227.119 Da
• Monoisotopic Mass: 227.119 Da
• Topological Polar Surface Area: 85.800 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 123.000
• 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. Li Shuai, Yang Shenghai, Wang Changhong.  (2022)  Electrochemical Behavior of Tetraethylammonium-Hydrogen Sulfate-Based Electrodissolution-Coupled Hafnium Alkoxide Synthesis.  JOM,  74  (9): (3548-3556).  [PMID:] [10.1007/s11837-022-05393-y]

2. Shuai Li, Shenghai Yang, Kangkang Li, Yanqing Lai, Chaoyong Deng, Changhong Wang.  (2022)  Electrodissolution-Coupled Hafnium Alkoxide Synthesis with High Environmental and Economic Benefits.  ChemSusChem,  15  (11): (e202200474).  [PMID:35365962] [10.1002/cssc.202200474]

3. Jielin Huang, Jie Wang, Haonan Duan, Songsong Chen, Junping Zhang, Li Dong, Xiangping Zhang.  (2024)  Constructing mesoporous CeO2 single-crystal particles in ionic liquids for enhancing the conversion of CO2 and alcohols to carbonates.  CHINESE JOURNAL OF CATALYSIS,      [PMID:] [10.1016/S1872-2067(24)60117-8]

4. Shuai LI, Sheng-hai YANG, Yong-ming CHEN, Chao-bo TANG, Yan-qing LAI, Chao-yong DENG, Chang-hong WANG.  (2024)  Electrochemical mechanism and kinetics of electrodissolution-coupled hafnium alkoxide synthesis in tetraethylammonium-chloride-based anhydrous system.  TRANSACTIONS OF NONFERROUS METALS SOCIETY OF CHINA,      [PMID:] [10.1016/S1003-6326(24)66499-X]