Tetraethylammonium bromide - for ion pair chromatography , CAS No.71-91-0

CAS: 71-91-0 Cat. No.: T103710 Formula: C₈H₂₀NBr Peso molecolare: 210.16 Numero EC: 200-769-4 PubChem CID: 6285

GRADE & PURITY for Ion pair chromatography

Synonyms

Etambro | Ethanaminium, N,N,N-triethyl-, bromide | Ethanaminium,N,N-triethyl-, bromide | JC10004 | NSC 36724 | Tox21_302138 | HWCKGOZZJDHMNC-UHFFFAOYSA-M | CAS-71-91-0 | Ethylon | TEAB | Tetraethyl ammonium bromide | Bromure de tetraethylammonium | Beparo

Storage

Room temperature,Desiccated

Shipped In

Normal

Specifications

Sinonimi

Etambro | Ethanaminium, N,N,N-triethyl-, bromide | Ethanaminium,N,N-triethyl-, bromide | JC10004 | NSC 36724 | Tox21_302138 | HWCKGOZZJDHMNC-UHFFFAOYSA-M | CAS-71-91-0 | Ethylon | TEAB | Tetraethyl ammonium bromide | Bromure de tetraethylammonium | Beparo

Specifiche e purezza

for ion pair chromatography

Condizioni di conservazione di stoccaggio

Room temperature,Desiccated

Spedito in

Normal

Grado

per la cromatografia a coppie ioniche

Nomi e identificatori

Pubchem Sid

508813036

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508813036

Sorrisi canonici

CC[N+](CC)(CC)CC.[Br-]

IUPAC Name

tetraethylazanium;bromide

InChIKey

HWCKGOZZJDHMNC-UHFFFAOYSA-M

INCHI

1S/C8H20N.BrH/c1-5-9(6-2,7-3)8-4;/h5-8H2,1-4H3;1H/q+1;/p-1

Isomeri SMILES

CC[N+](CC)(CC)CC.[Br-]

RTECS

BS5950000

CAS alternativo

71-91-0,66-40-0 (Parent)

PubChem CID

6285

Numero NSC

36724

Termini MeSH

Bromide, Tetraethylammonium;Chloride, Tetraethylammonium;Hydroxide, Tetraethylammonium;Iodide, Tetraethylammonium;Ion, Tetraethylammonium;Tetraethylammonium;Tetraethylammonium Bromide;Tetraethylammonium Chloride;Tetraethylammonium Hydroxide;Tetraethylammo

Peso molecolare

210.16

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: 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
• Descrizione: 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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Sensibilità: Hygroscopic.
• Punto di fusione (°C): 285°C(dec.)(lit.)
• Peso molecolare: 210.160 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 209.078 Da
• Monoisotopic Mass: 209.078 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 47.500
• 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