Triethanolamine acetate

Base Information

• Chemical Name: Triethanolamine acetate
• CAS No.: 67924-03-2
• Molecular Formula: C8H19NO5
• Molecular Weight: 209.2402
• European Community (EC) Number: 238-874-2,614-176-7
• UNII: Y40P5N140O
• Wikidata: Q27294237
• Mol file: 67924-03-2.mol

Synonyms:2,2',2''-nitrilotriethanol;triethanolamine;triethanolamine acetate;triethanolamine citrate;triethanolamine citrate (1:1);triethanolamine copper salt;triethanolamine hydrochloride;triethanolamine iodohydrate;triethanolamine maleate;triethanolamine phosphate;triethanolamine sulfate;triethanolamine sulfate (2:1);triethanolamine sulfite (1:1);triethanolamine tartrate (1:1), (R-(R*,R*))-isomer;triethanolamine titanium salt;triethanolammonium chloride;trolamine

Chemical Property of Triethanolamine acetate

Chemical Property:

• Boiling Point: 335.4°Cat760mmHg
• Flash Point: 185°C
• Density: g/cm³
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 6
• Exact Mass: 209.12632271
• Heavy Atom Count: 14
• Complexity: 86.8

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(=O)O.C(CO)N(CCO)CCO

Technology Process of Triethanolamine acetate

There total 3 articles about Triethanolamine 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:

triethanolamine (102-71-6,64114-46-1) + acetic acid (64-19-7,77671-22-8) → triethanolammonium acetate (14806-72-5,67924-03-2)

Guidance literature:

In neat (no solvent); at 20 ℃; for 2h;

DOI:10.1002/jccs.201700019

Reference yield:

triethanolamine (102-71-6,64114-46-1) + acetic acid (64-19-7,77671-22-8) → 49.9C2H4O2*50.1C6H15NO3 (67924-03-2)

Guidance literature:

Neat (no solvent);

DOI:10.1039/b921432a

Reference yield:

→ triethanolammonium acetate (14806-72-5,67924-03-2)

Guidance literature:

In water; at 20 ℃; for 3h;

upstream raw materials:

triethanolamine

acetic acid

Refernces

• 1、 Chen, Qianhan,Cheng, Shuang,Fan, Dongshuang,Feng, Wanlu,Guo, Yuanyang,Li, Lingjun,Li, Zhiyong,Wang, Jianji,Zhu, Anlian. "Cleaner enzymatic production of biodiesel with easy separation procedures triggered by a biocompatible hydrophilic ionic liquid". . p. 1944 - 1951. Retrieved 2020/04/09.
• 2、 -. "The hydrophilic ionic liquid at room temperature and its use". Paragraph 0105; 0106. . Retrieved 2019/09/11.