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N-Vinylcaprolactam

Base Information Edit
  • Chemical Name:N-Vinylcaprolactam
  • CAS No.:25189-83-7
  • Deprecated CAS:146876-34-8,266309-50-6,1280200-98-7,1453194-36-9,266309-50-6
  • Molecular Formula:C8H13NO
  • Molecular Weight:139.19492
  • Hs Code.:
  • European Community (EC) Number:218-787-6
  • UNII:KFC10CY9UP
  • DSSTox Substance ID:DTXSID1041423
  • Nikkaji Number:J213.131E
  • Wikidata:Q15712394
  • RXCUI:2534441
  • ChEMBL ID:CHEMBL3188330
  • Mol file:25189-83-7.mol
N-Vinylcaprolactam

Synonyms:oligo(N-vinylcaprolactam);poly(N-vinylcaprolactam);poly-N-vinylcaprolactam

Suppliers and Price of N-Vinylcaprolactam
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
Total 31 raw suppliers
Chemical Property of N-Vinylcaprolactam Edit
Chemical Property:
  • Boiling Point:254.7°Cat760mmHg 
  • Flash Point:112.5°C 
  • Density:1.049g/cm3 
  • XLogP3:1.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:139.099714038
  • Heavy Atom Count:10
  • Complexity:142
Purity/Quality:

99%, *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Chemical Classes:Plastics & Rubber -> Other Monomers
  • Canonical SMILES:C=CN1CCCCCC1=O
Technology Process of N-Vinylcaprolactam

There total 6 articles about N-Vinylcaprolactam 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: 95.0%

Guidance literature:
With surface modified hydroxyapatite; at 220 ℃;
Guidance literature:
Guidance literature:
With dmap; [bis(2-methylallyl)cycloocta-1,5-diene]ruthenium(II); tributylphosphine; In toluene; at 100 ℃; for 16h; Reagent/catalyst; Autoclave; Glovebox;
DOI:10.1039/d0cc01533d
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