Triethyl ammonium acetate

Base Information

• Chemical Name: Triethyl ammonium acetate
• CAS No.: 5204-74-0
• Molecular Formula: C8H19NO2
• Molecular Weight: 161.244
• Hs Code.: 2921199090
• Mol file: 5204-74-0.mol

Synonyms:triethyl ammonium acetate;SCHEMBL22152

Chemical Property of Triethyl ammonium acetate

Chemical Property:

• Appearance/Colour: colourless liquid
• Melting Point: -18 °C
• Refractive Index: n20/D 1.357
• Boiling Point: 90.5 °C at 760 mmHg
• Flash Point: 98.4 °C
• PSA: 40.54000
• Density: 1.010 g/mL at 20 °C
• LogP: 1.43900
• Storage Temp.: 2-8°C
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 161.141578849
• Heavy Atom Count: 11
• Complexity: 51.2

Purity/Quality:

99% ^*data from raw suppliers

Triethylammonium Acetate, 1 M Solution ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C
• Hazard Codes: C,Xi
• Statements: 35-36/37/38-34
• Safety Statements: 26-36/37/39-45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC[NH+](CC)CC.CC(=O)[O-]
• Uses: Triethylammonium acetate buffer has been used for visualizing and quantifying single mRNA molecules in mammalian (mouse and human) tissues.

Technology Process of Triethyl ammonium acetate

There total 5 articles about Triethyl ammonium acetate 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: 98.0%

acetic acid (64-19-7,77671-22-8) + triethylamine (121-44-8) → triethylammonium acetate (5204-74-0)

Guidance literature:

at 70 - 80 ℃; for 3h;

DOI:10.1007/s00706-008-0886-4 DOI:10.1021/jp101209j

Reference yield:

triethylammonium triacetatouranylate → uranyl diacetate (17442-23-8,541-09-3) + triethylammonium acetate (5204-74-0)

Guidance literature:

In neat (no solvent); thermolysis in the absence of O2;

Reference yield:

1,4,10,13-tetraoxa-7,16-diazacyclooctadecane-7-acetic acid monohydrate + copper(II) acetate monohydrate (6046-93-1) → trans-acetato(1,4,10,13-tetraoxa-7,16-diazacyclooctadecane-7-acetato)copper(II) + triethylammonium acetate (5204-74-0)

Guidance literature:

With triethylamine; In methanol; refluxed for 1 h; removal of solvent in vac., addn. of acetone and triethylamine, left overnight in the refrigerator, filtered off, dried over P4O10; elem. anal.;

DOI:10.1016/S0277-5387(00)86395-0

upstream raw materials:

acetic acid

triethylamine

copper(II) acetate monohydrate

Downstream raw materials:

17α,21-dihydroxypregna-1,4-diene-3,20-dione 21-acetate

P₁-uridine 5-P₃-phenyltriphosphate triethylammonium salt

Refernces

• 1、 Zhao, Shuo,He, Man,Zhou, Yuming,Sheng, Xiaoli,Fu, Xiaoqin,Zhang, Yiwei. "Synthesis of micro/mesoporous silica material by duallate method as a heterogeneous catalyst support for alkylation". . p. 28124 - 28132. Retrieved 2015.
• 2、 Lv, Yi Qi,Guo, Yan,Luo, Xiao Yan,Li, Hao Ran. "Infrared spectroscopic study on chemical and phase equilibrium in triethylammonium acetate". . p. 1688 - 1694,7. Retrieved 2012.
• 3、 Zhu, Anlian,Li, Qixing,Feng, Wanlu,Fan, Dongshuang,Li, Lingjun. "Biocompatible Ionic Liquid Promote One-Pot Synthesis of 2-Amino-4H-Chromenes Under Ambient Conditions". . p. 720 - 733. Retrieved 2020/08/07.