N-(2-Hydroxyethyl)tetradecanamide

Base Information

• Chemical Name: N-(2-Hydroxyethyl)tetradecanamide
• CAS No.: 142-58-5
• Molecular Formula: C16H33 N O2
• Molecular Weight: 271.444
• Hs Code.: 2924199090
• European Community (EC) Number: 205-546-5
• UNII: 6CYG57WXZ0
• DSSTox Substance ID: DTXSID0042452
• Nikkaji Number: J115.314E
• Wikidata: Q27083876
• Metabolomics Workbench ID: 4686
• Mol file: 142-58-5.mol

Synonyms:N-myristoylethanolamine

Chemical Property of N-(2-Hydroxyethyl)tetradecanamide

Chemical Property:

• Vapor Pressure: 1.91E-09mmHg at 25°C
• Melting Point: 93-94 °C
• Boiling Point: 436.3°Cat760mmHg
• PKA: 14.49±0.10(Predicted)
• Flash Point: 217.7°C
• PSA: 49.33000
• Density: 0.916g/cm³
• LogP: 4.18690
• Storage Temp.: Sealed in dry,Room Temperature
• XLogP3: 5.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 14
• Exact Mass: 271.251129295
• Heavy Atom Count: 19
• Complexity: 195

Purity/Quality:

99%, ^*data from raw suppliers

N-(2-Hydroxyethyl)tetradecanamide 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Nitrogen Compounds -> Other Nitrogen Compounds
• Canonical SMILES: CCCCCCCCCCCCCC(=O)NCCO

Technology Process of N-(2-Hydroxyethyl)tetradecanamide

There total 6 articles about N-(2-Hydroxyethyl)tetradecanamide 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: 98.0%

ethanolamine (141-43-5) + tetradecanoyl chloride (112-64-1) → myristic monoethanolamide (142-58-5)

Guidance literature:

In dichloromethane; for 1h;

DOI:10.1080/14756366.2021.1912035

Reference yield: 97.3%

Ethyl myristate (124-06-1) + ethanolamine (141-43-5) → myristic monoethanolamide (142-58-5)

Guidance literature:

With Novozym 435; In 1,4-dioxane; for 0.075h; chemoselective reaction; Microwave irradiation; Enzymatic reaction;

DOI:10.3762/bjoc.5.10

Reference yield: 97.2%

ethanolamine (141-43-5) + n-tetradecanoic acid (544-63-8) → myristic monoethanolamide (142-58-5)

Guidance literature:

With Novozym 435; In 1,4-dioxane; for 0.075h; chemoselective reaction; Microwave irradiation; Enzymatic reaction;

DOI:10.3762/bjoc.5.10

upstream raw materials:

methyl myristoate

ethanolamine

Ethyl myristate

tetradecanoyl chloride

Downstream raw materials:

N-dodecanoylglycine

N-myristoylglycine

N-palmitoyl glycine

N-stearoylglycine

Refernces

• 1、 Pal, Amrita,Mahapatra, Rita Das,Dey, Joykrishna. "Comparison of the gelation behaviour of N-substituted tetradecanamide amphiphiles in organic liquids: Effect of hydrogen-bonding ability of the head-group". . p. 7760 - 7765. Retrieved 2014.
• 2、 -. "Methods for production of fatty acid alkanolamides (FAAAs) from microalgae biomass". Page/Page column 11; 12. . Retrieved 2017/02/28.