Acetamide, 2-hydroxy-N,N-bis(2-hydroxyethyl)-

Base Information

• Chemical Name: Acetamide, 2-hydroxy-N,N-bis(2-hydroxyethyl)-
• CAS No.: 17409-41-5
• Molecular Formula: C₆H₁₃NO₄
• Molecular Weight: 163.174
• Hs Code.: 2924199090
• NSC Number: 274597
• UNII: 2Y8JET6THE
• DSSTox Substance ID: DTXSID2066195
• Nikkaji Number: J421.989I
• Wikidata: Q81992778
• ChEMBL ID: CHEMBL509252
• Mol file: 17409-41-5.mol

Synonyms:2-Hydroxy-N,N-bis(2-hydroxyethyl)acetamide;17409-41-5;Acetamide, 2-hydroxy-N,N-bis(2-hydroxyethyl)-;N,N-Bis(2-hydroxyethyl)glycolamide;Glycolamide, N,N-bis(2-hydroxyethyl)-;AI3-63111;2Y8JET6THE;NSC 274597;NSC-274597;ACETAMIDE,2-HYDROXY-N,N-BIS(2-HYDROXYETHYL)-;NSC274597;N-glycolyl-diethanolamine;UNII-2Y8JET6THE;CHEMBL509252;SCHEMBL1387475;DTXSID2066195;Acetamide,N-bis(2-hydroxyethyl)-;Glycolamide,N-bis(2-hydroxyethyl)-;N,N-bis(hydroxyethyl)hydroxyacetamide;AKOS006278229;N,N-bis(hydroxyethyl) hydroxyacetamide;LS-72906

Chemical Property of Acetamide, 2-hydroxy-N,N-bis(2-hydroxyethyl)-

Chemical Property:

• Vapor Pressure: 1.24E-07mmHg at 25°C
• Boiling Point: 388.3°Cat760mmHg
• Flash Point: 188.6°C
• PSA: 81.00000
• Density: 1.31g/cm³
• LogP: -2.20810
• XLogP3: -2.3
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 163.08445790
• Heavy Atom Count: 11
• Complexity: 111

Purity/Quality:

99% ^*data from raw suppliers

GLYCOLAMIDE, N,N-BIS(2-HYDROXYETHYL)- 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of Acetamide, 2-hydroxy-N,N-bis(2-hydroxyethyl)-

There total 1 articles about Acetamide, 2-hydroxy-N,N-bis(2-hydroxyethyl)- 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: 15.0%

4-oxo-2,2-dimethyl-1,3-dioxolane (4158-86-5) + 2,2'-iminobis[ethanol] (111-42-2) → 2-hydroxy-N,N-bis(2-hydroxyethyl)acetamide (17409-41-5)

Guidance literature:

In dichloromethane; at 20 ℃; Inert atmosphere;

DOI:10.1016/j.ejmech.2008.02.022

Reference yield:

2-hydroxy-N,N-bis(2-hydroxyethyl)acetamide (17409-41-5) + Trimethyl borate (121-43-7,63156-11-6) → C6H10BNO4

Guidance literature:

In toluene; for 20.5h; Reflux;

upstream raw materials:

4-oxo-2,2-dimethyl-1,3-dioxolane

2,2'-iminobis[ethanol]

Refernces