Ethanaminium, N,N,N-trimethyl-, hydroxide

Base Information

• Chemical Name: Ethanaminium, N,N,N-trimethyl-, hydroxide
• CAS No.: 30382-83-3
• Molecular Formula: C5H14 N . H O
• Molecular Weight: 105.18
• European Community (EC) Number: 608-473-0
• DSSTox Substance ID: DTXSID5067552
• Mol file: 30382-83-3.mol

Synonyms:Ethanaminium, N,N,N-trimethyl-, hydroxide;30382-83-3;Ethyltrimethylammonium hydroxide;ethyl(trimethyl)azanium;hydroxide;Ethanaminium, N,N,N-trimethyl-, hydroxide (1:1);Trimethylathylammoniumhydroxyd;C5H14N.HO;ethyltrimethylazanium hydroxide;SCHEMBL187547;DTXSID5067552;C5-H14-N.H-O

Chemical Property of Ethanaminium, N,N,N-trimethyl-, hydroxide

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 23.06000
• Density: g/cm³
• LogP: 0.53570
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 105.115364102
• Heavy Atom Count: 7
• Complexity: 33.7

Purity/Quality:

99.9% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC[N+](C)(C)C.[OH-]
• Use Description: ETHYLTRIMETHYLAMMONIUM HYDROXIDE is a quaternary ammonium compound with various applications across different fields. In organic synthesis and chemical research, it serves as a phase-transfer catalyst facilitating reactions between immiscible phases, typically between organic and aqueous phases. Its role is crucial in promoting efficient chemical reactions by enabling reactants to move between these phases and enhancing reaction yields. In the field of analytical chemistry, it can be utilized as a reagent for the determination of certain analytes through ion chromatography or other analytical techniques. Its use in this context aids in the quantification and analysis of specific ions or compounds. Furthermore, in the pharmaceutical and biochemical industries, it may find application as a reactant or intermediate in the synthesis of various organic compounds or as an agent for protein or nucleic acid extraction. Its significance varies within these fields, but it consistently plays a pivotal role in advancing chemical reactions, analytical methods, and organic synthesis across diverse scientific and industrial applications.

Technology Process of Ethanaminium, N,N,N-trimethyl-, hydroxide

There total 2 articles about Ethanaminium, N,N,N-trimethyl-, hydroxide 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:

ethyltrimethylammonium iodide (51-93-4) → trimethylethylammonium hydroxide (30382-83-3)

Guidance literature:

With anion exchange resin DOWEX 1X-8;

Reference yield:

→ trimethylethylammonium hydrogencarbonate (117442-31-6) + trimethylethylammonium hydroxide (30382-83-3)

Guidance literature:

Reference yield:

trimethylethylammonium hydroxide (30382-83-3) + acetic acid (64-19-7,77671-22-8) → ethyltrimethylammonium acetate

Guidance literature:

With amberlyst A₂₆; In methanol; at 20 ℃; for 12h;

DOI:10.1039/c8gc03549k

upstream raw materials:

ethyltrimethylammonium iodide

Downstream raw materials:

ethene

water

trimethylamine

Refernces

• 1、 Ono, Hiroshi,Ikeda, Ryuichi,Ishida, Hiroyukl. "Ionic motions and phase transitions in solid trimethylethylammonium tetrafluroberate studied by by1H, 19F, and14N NMR, powder X-ray diffraction and differential scanning calorimetry". . p. 1833 - 1838. Retrieved 2007/10/03.