N-Hexadecylacrylamide

Base Information

• Chemical Name: N-Hexadecylacrylamide
• CAS No.: 21216-80-8
• Molecular Formula: C19H37 N O
• Molecular Weight: 295.509
• Hs Code.: 2924199090
• European Community (EC) Number: 244-278-3
• DSSTox Substance ID: DTXSID20175446
• Nikkaji Number: J107.695G
• Wikidata: Q83045788
• Mol file: 21216-80-8.mol

Synonyms:N-Hexadecylacrylamide;21216-80-8;N-hexadecylprop-2-enamide;2-Propenamide, N-hexadecyl-;N-cetylacrylamide;SCHEMBL252114;DTXSID20175446;EINECS 244-278-3

Chemical Property of N-Hexadecylacrylamide

Chemical Property:

• Vapor Pressure: 1.29E-07mmHg at 25°C
• Boiling Point: 430.5°Cat760mmHg
• Flash Point: 267.9°C
• PSA: 32.59000
• Density: 0.861g/cm³
• LogP: 6.61020
• XLogP3: 7.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 16
• Exact Mass: 295.287514804
• Heavy Atom Count: 21
• Complexity: 238

Purity/Quality:

98%Min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCCNC(=O)C=C

Technology Process of N-Hexadecylacrylamide

There total 3 articles about N-Hexadecylacrylamide 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: 65.0%

1-Chlorohexadecan (4860-03-1) + 2-propenamide (79-06-1,12624-24-7,25038-45-3,27754-57-0,33338-03-3,39387-77-4,68247-81-4,9082-06-8,79079-15-5) → N-cetylacrylamide (21216-80-8)

Guidance literature:

1-Chlorohexadecan; 2-propenamide; aluminum (III) chloride; In acetone; at 20 ℃; for 0.0833333 - 0.166667h;

at 40 - 50 ℃;

Reference yield:

hexadecylamine (143-27-1) + acryloyl chloride (814-68-6,25189-84-8) → N-cetylacrylamide (21216-80-8)

Guidance literature:

With TEA; In dichloromethane; at 0 - 20 ℃;

DOI:10.1021/jm000508c

Reference yield:

→ N-cetylacrylamide (21216-80-8)

Guidance literature:

Cetylamin, Acrylchlorid;

upstream raw materials:

hexadecylamine

acryloyl chloride

1-Chlorohexadecan

2-propenamide

Downstream raw materials:

(E)-3-(4-{2-[4-((E)-2-Hexadecylcarbamoyl-vinyl)-phenyl]-2-oxo-acetyl}-phenyl)-acrylic acid tert-butyl ester

3-(4-{4-[4-((E)-2-tert-butoxycarbonyl-vinyl)phenyl]-5-[4-(2-hexadecylcarbamoyl-vinyl)phenyl]-1H-imidazol-2-yl}phenyl)-4,5-dihydroisoxazole-5-carboxylic acid tert-butyl ester

3-(4-{4-[4-((E)-2-tert-butoxycarbonyl-vinyl)phenyl]-5-[4-(2-hexadecylcarbamoyl-vinyl)phenyl]-1H-imidazol-2-yl}phenyl)-isoxazole-5-carboxylic acid ethyl ester

3-(4-{4-[4-((E)-2-Carboxy-vinyl)-phenyl]-5-[4-((E)-2-hexadecylcarbamoyl-vinyl)-phenyl]-1H-imidazol-2-yl}-phenyl)-4,5-dihydro-isoxazole-5-carboxylic acid

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