Ethanolamine acetate

Base Information

• Chemical Name: Ethanolamine acetate
• CAS No.: 54300-24-2
• Molecular Formula: C4H11NO3
• Molecular Weight: 121.136
• Hs Code.: 2923900090
• European Community (EC) Number: 259-078-1
• DSSTox Substance ID: DTXSID5068940
• Wikidata: Q27288467
• Mol file: 54300-24-2.mol

Synonyms:ethanolamine acetate;2-Aminoethanol acetate;54300-24-2;Ethanol, 2-amino-, acetate (salt);2-Aminoethanolacetate;Ethanolamine acetate (salt);SCHEMBL503041;UNII-S20U1L1S25;DTXSID5068940;EINECS 259-078-1;Q27288467

Chemical Property of Ethanolamine acetate

Chemical Property:

• Vapor Pressure: 0.458mmHg at 25°C
• Melting Point: 65-66 °C
• Boiling Point: 170.9°C at 760 mmHg
• Flash Point: 93.3°C
• PSA: 83.55000
• Density: 1.120 g/cm3(Temp: 166.0 °C Press: 4.80 Torr)
• LogP: -0.27140
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 121.07389321
• Heavy Atom Count: 8
• Complexity: 41

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)O.C(CO)N

Technology Process of Ethanolamine acetate

There total 2 articles about Ethanolamine 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: 93.0%

ethanolamine (141-43-5) + acetic acid (64-19-7,77671-22-8) → (2-hydroxy-ethyl)ammonium acetate (54300-24-2)

Guidance literature:

at 0 - 20 ℃; for 24.5h; Inert atmosphere;

DOI:10.1080/00397911.2013.867505

Reference yield:

→ (2-hydroxy-ethyl)ammonium acetate (54300-24-2)

Guidance literature:

In water; at 20 ℃; for 3h;

Reference yield: 62.0%

potassium thioacyanate (333-20-0) + (2-hydroxy-ethyl)ammonium acetate (54300-24-2) + desyl bromide (1484-50-0) → 4,5-diphenyl-2-(2-hydroxyethylamino)thiazole (57639-14-2)

Guidance literature:

With aluminum oxide; silica gel; In benzene; at 80 ℃; for 6h;

DOI:10.1016/j.tet.2006.01.075

upstream raw materials:

ethanolamine

acetic acid

Downstream raw materials:

2-(2-hydroxyethylamino)-4-methylthiazole

2-N-(β-hydroxyethylamino)-4-phenylthiazole

4,5-diphenyl-2-(2-hydroxyethylamino)thiazole

2-Anilinoethanol

Refernces

• 1、 Cong, Yu,Li, Guangyi,Li, Ning,Wang, Aiqin,Wang, Ran,Wang, Xiaodong,Xu, Jilei,Zhang, Tao. "Synthesis of renewable alkylated naphthalenes with benzaldehyde and angelica lactone". supporting information. p. 5474 - 5480. Retrieved 2021/08/16.
• 2、 Abraham, Amanda N.,Arunkumar, Radhika,Drummond, Calum J.,Greaves, Tamar L.,Shukla, Ravi. "Cytotoxicity of protic ionic liquids towards the HaCat cell line derived from human skin". . . Retrieved 2020/07/03.