Tetraethylammonium

Base Information

• Chemical Name: Tetraethylammonium
• CAS No.: 66-40-0
• Molecular Formula: C8H20N
• Molecular Weight: 130.254
• NSC Number: 156315,152122
• UNII: 5AV7G7EIEE
• DSSTox Substance ID: DTXSID2045024
• Nikkaji Number: J91.253K
• Wikipedia: Tetraethylammonium
• Wikidata: Q410728
• Pharos Ligand ID: J3RVSY2X355U
• Metabolomics Workbench ID: 52372
• ChEMBL ID: CHEMBL9324
• Mol file: 66-40-0.mol

Synonyms:Bromide, Tetraethylammonium;Chloride, Tetraethylammonium;Hydroxide, Tetraethylammonium;Iodide, Tetraethylammonium;Ion, Tetraethylammonium;Tetraethylammonium;Tetraethylammonium Bromide;Tetraethylammonium Chloride;Tetraethylammonium Hydroxide;Tetraethylammonium Iodide;Tetraethylammonium Ion

Chemical Property of Tetraethylammonium

Chemical Property:

• Melting Point: 223 °C (decomp)
• Refractive Index: 1.4525 (estimate)
• Boiling Point: 231°C (rough estimate)
• PSA: 0.00000
• Density: 0.7930 (rough estimate)
• LogP: 1.88280
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 4
• Exact Mass: 130.159574642
• Heavy Atom Count: 9
• Complexity: 47.5

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC[N+](CC)(CC)CC
• Recent ClinicalTrials: Endothelial Hyperpolarization in Humans

Technology Process of Tetraethylammonium

There total 2 articles about Tetraethylammonium which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

diethyl chlorophosphate (814-49-3) + triethylamine (121-44-8) + benzene (71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1) → triethyl phosphate (78-40-0) + chloroethane (75-00-3) + tetraethyl ammonium (66-40-0)

Guidance literature:

Reference yield:

{(C2H5)4N}(1+)*{BI4}(1-)={(C2H5)4N}{BI4} (23289-77-2) → {BI2}(1+) + tetraethyl ammonium (66-40-0) + iodide (14362-44-8,20461-54-5,69239-56-1)

Guidance literature:

In acetonitrile; dissociation in CH3CN;; not isolated, by measurement of electrolytic conductivity;;

Reference yield: 90.0%

(η5-methylcyclopentadienyl)dicarbonyl(hydrido)(triphenylgermyl)manganese (90148-95-1) + tetraethyl ammonium (66-40-0) → tetraethylammonium (η5-methylcyclopentadienyl)dicarbonyl(triphenylgermyl)manganese (68168-06-9)

Guidance literature:

With NaH; In tetrahydrofuran; Complex was treated with NaH in THF at room temp., 1 h (N2 atm.);;

upstream raw materials:

diethyl chlorophosphate

triethylamine

benzene

{(C₂H₅)4N}⁽¹⁺⁾*{BI₄}^(1-)={(C₂H₅)4N}{BI₄}

Downstream raw materials:

oxo-bis

ethene

triethylamine

formic acid

Refernces