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N-Octadecyl methacrylamide

Base Information Edit
  • Chemical Name:N-Octadecyl methacrylamide
  • CAS No.:7283-61-6
  • Molecular Formula:C22H43NO
  • Molecular Weight:337.59
  • Hs Code.:2924199090
  • DSSTox Substance ID:DTXSID20440161
  • Nikkaji Number:J1.068.332G
  • Wikidata:Q82256396
  • Mol file:7283-61-6.mol
N-Octadecyl methacrylamide

Synonyms:N-OCTADECYL METHACRYLAMIDE;7283-61-6;2-methyl-N-octadecylprop-2-enamide;N-OCTADECYLMETHACRYLAMIDE;n-stearylmethacrylamide;SCHEMBL144546;DTXSID20440161;MFCD00080599;FT-0702985

Suppliers and Price of N-Octadecyl methacrylamide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • N-OCTADECYLMETHACRYLAMIDE 95.00%
  • 5MG
  • $ 501.92
Total 3 raw suppliers
Chemical Property of N-Octadecyl methacrylamide Edit
Chemical Property:
  • PSA:29.10000 
  • LogP:7.33110 
  • XLogP3:9.3
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:18
  • Exact Mass:337.334464995
  • Heavy Atom Count:24
  • Complexity:298
Purity/Quality:

97% *data from raw suppliers

N-OCTADECYLMETHACRYLAMIDE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Statements: 36/37/38 
  • Safety Statements: 26-36/37/39 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCCCCCCCCCCNC(=O)C(=C)C
Technology Process of N-Octadecyl methacrylamide

There total 2 articles about N-Octadecyl methacrylamide 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:
Guidance literature:
With triethylamine; In monoethylene glycol diethyl ether; water; at 20 - 40 ℃; for 2h; Inert atmosphere;
Guidance literature:
With 10H-phenothiazine; 4-methoxy-phenol; magnesium chloride; In tetrahydrofuran; at 70 ℃; for 4h; Inert atmosphere;
upstream raw materials:

1-aminooctadecane

Methacryloyl chloride

Refernces Edit
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