Stearic monoethanolamide stearate

Base Information

• Chemical Name: Stearic monoethanolamide stearate
• CAS No.: 14351-40-7
• Molecular Formula: C38H75NO3
• Molecular Weight: 594.018
• Hs Code.: 2924199090
• European Community (EC) Number: 238-310-5
• UNII: L3WR6PEQ9J
• DSSTox Substance ID: DTXSID1051721
• Nikkaji Number: J216.979G
• Wikidata: Q27282662
• Mol file: 14351-40-7.mol

Synonyms:Stearic monoethanolamide stearate;14351-40-7;Stearamide MEA-stearate;2-(octadecanoylamino)ethyl octadecanoate;UNII-L3WR6PEQ9J;L3WR6PEQ9J;Ethanolamine N,o-distearate;2-((1-Oxooctadecyl)amino)ethyl octadecanoate;EINECS 238-310-5;Octadecanoic acid, 2-((1-oxooctadecyl)amino)ethyl ester;2-[(1-oxooctadecyl)amino]ethyl stearate;STEAROYL MONOETHANOLAMIDE STEARATE;Octadecanoic acid, 2-[(1-oxooctadecyl)amino]ethyl ester;2-((1-Oxooctadecyl)amino)ethyl stearate;2-stearamidoethyl stearate;SCHEMBL303966;DTXSID1051721;C38H75NO3;C38-H75-N-O3;STEARAMIDE MEA-STEARATE [INCI];STEARAMIDE MEA-STEARATE [VANDF];Stearic acid 2-(stearoylamino)ethyl ester;2- [(1- oxooctadecyl)amino]ethyl stearate;Q27282662

Chemical Property of Stearic monoethanolamide stearate

Chemical Property:

• Vapor Pressure: 2.93E-18mmHg at 25°C
• Melting Point: 92-94 °C(Solv: ethanol (64-17-5))
• Refractive Index: 1.463
• Boiling Point: 678.4 °C at 760 mmHg
• PKA: 15.32±0.46(Predicted)
• Flash Point: 364.1 °C
• PSA: 58.89000
• Density: 0.892 g/cm³
• LogP: 13.00910
• XLogP3: 16.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 36
• Exact Mass: 593.57469525
• Heavy Atom Count: 42
• Complexity: 551

Purity/Quality:

99% ^*data from raw suppliers

STEAROYL MONOETHANOLAMIDE STEARATE 97.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCCCC(=O)NCCOC(=O)CCCCCCCCCCCCCCCCC

Technology Process of Stearic monoethanolamide stearate

There total 7 articles about Stearic monoethanolamide stearate 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:

ethanolamine (141-43-5) + stearic acid (57-11-4) → N-stearoylethanolamine (111-57-9,8038-89-9) + stearic acid monoethanolamide stearate (14351-40-7)

Guidance literature:

With zeolite H-beta-150; In hexane; at 180 ℃; for 3h; under 15001.5 Torr; Reagent/catalyst; Inert atmosphere;

DOI:10.1002/cssc.201500526

Reference yield:

ethanolamine (141-43-5) + stearic acid (57-11-4) → stearic acid monoethanolamide stearate (14351-40-7)

Guidance literature:

With Lipozyme IM-20; In chloroform; at 60 ℃; for 16h;

Reference yield:

N-stearoylethanolamine (111-57-9,8038-89-9) → stearic acid monoethanolamide stearate (14351-40-7)

Guidance literature:

In water; at 220 - 230 ℃;

upstream raw materials:

N-stearoylethanolamine

O-stearoylethanolamine

stearic acid

ethanolamine

Downstream raw materials:

2-heptadecyl-2-imidazoline

Refernces

• 1、 Tkacheva, Anastasia,Dosmagambetova, Inkar,Chapellier, Yann,M?ki-Arvela, P?ivi,Hachemi, Imane,Savela, Risto,Leino, Reko,Viegas, Carolina,Kumar, Narendra,Er?nen, Kari,Hemming, Jarl,Smeds, Annika,Murzin, Dmitry Yu.. "Pharmaceuticals and Surfactants from Alga-Derived Feedstock: Amidation of Fatty Acids and Their Derivatives with Amino Alcohols". . p. 2670 - 2680. Retrieved 2015/09/02.
• 2、 -. "Amide esters as hydrocarbon gellants". Page/Page column 5-6. . Retrieved 2008/06/13.