Acetamide, 2,2'-oxybis[N,N-dioctyl-

Base Information

• Chemical Name: Acetamide, 2,2'-oxybis[N,N-dioctyl-
• CAS No.: 342794-43-8
• Molecular Formula: C₃₆H₇₂N₂O₃
• Molecular Weight: 580.979
• Mol file: 342794-43-8.mol

Synonyms:N,N,N',N'-tetraoctyl diglycolamide;Acetamide,2,2'-oxybis[N,N-dioctyl;2,2'-Oxybis(N,N-dioctylacetamide);

Chemical Property of Acetamide, 2,2'-oxybis[N,N-dioctyl-

Chemical Property:

• Boiling Point: 652.6±40.0 °C(Predicted)
• PKA: -0.53±0.70(Predicted)
• PSA: 49.85000
• Density: 0.910±0.06 g/cm3(Predicted)
• LogP: 10.10220
• Storage Temp.: Sealed in dry,Room Temperature

Purity/Quality:

99% ^*data from raw suppliers

2,2'-Oxybis(N,N-di-n-octylacetamide) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Use Description: Acetamide, 2,2'-oxybis[N,N-dioctyl-], a specific chemical compound, serves diverse functions across different fields. In the realm of materials science and polymer chemistry, it plays a pivotal role as a plasticizer and softening agent in the production of flexible and durable plastics and polymers, contributing to the development of materials used in various industries, including automotive, construction, and packaging. In the field of organic synthesis and chemical research, this compound can serve as a reagent or building block for the creation of specialized organic molecules, aiding in the development of new chemical compounds and processes. Moreover, in analytical chemistry, it may be employed as a reference material or standard for calibration purposes, ensuring accurate measurements and chemical analysis. Its applications in materials science, organic synthesis, and analytical chemistry underscore its significance in enhancing material properties, facilitating chemical innovation, and supporting precise chemical analysis within these diverse domains.

Technology Process of Acetamide, 2,2'-oxybis[N,N-dioctyl-

There total 4 articles about Acetamide, 2,2'-oxybis[N,N-dioctyl- 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: 94.0%

n-dioctylamine (1120-48-5) + diglycolyl chloride (21062-20-4) → TODGA (342794-43-8)

Guidance literature:

With sodium hydroxide; In diethyl ether; water; at 20 ℃; for 2.5h; Temperature;

DOI:10.1055/s-0035-1561495

Reference yield: 85.0%

diethyl diglycolate (6634-17-9) + n-dioctylamine (1120-48-5) → TODGA (342794-43-8)

Guidance literature:

With aluminum (III) chloride; triethylamine; In dichloromethane; at 20 ℃; for 2.5h;

DOI:10.1055/s-0035-1561495

Reference yield: 83.0%

n-dioctylamine (1120-48-5) + dimethyl diglycolate (7040-23-5) → TODGA (342794-43-8)

Guidance literature:

With aluminum (III) chloride; triethylamine; In dichloromethane; at 20 ℃; for 2.5h;

DOI:10.1055/s-0035-1561495

upstream raw materials:

n-dioctylamine

diglycolyl chloride

dimethyl diglycolate

diethyl diglycolate

Refernces

• 1、 -. "Novel process for synthesizing N,N,N',N'-tetraoctyl-3-oxyglutaramide". Paragraph 0026; 0028-0030; 0032-0034; 0036; 0037. . Retrieved 2019/07/04.