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Glycidyl Myristate

Base Information Edit
  • Chemical Name:Glycidyl Myristate
  • CAS No.:7460-80-2
  • Molecular Formula:C17H32O3
  • Molecular Weight:284.439
  • Hs Code.:
  • Mol file:7460-80-2.mol
Glycidyl Myristate

Synonyms:Glycidyl Tetradecanoate;myristic acid-(2,3-epoxy-propyl ester);Myristic Acid Glycidyl Ester;Glycidyl Myristate;Myristinsaeureglycidester;tetradecanoyloxymethyl-oxirane;Myristinsaeure-(2,3-epoxy-propylester);

Suppliers and Price of Glycidyl Myristate
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
  • TRC
  • GlycidylMyristate
  • 100mg
  • $ 185.00
  • Usbiological
  • Glycidyl Myristate
  • 100mg
  • $ 460.00
Total 5 raw suppliers
Chemical Property of Glycidyl Myristate Edit
Chemical Property:
  • Vapor Pressure:1.45E-05mmHg at 25°C 
  • Boiling Point:366.6°Cat760mmHg 
  • Flash Point:142.6°C 
  • PSA:38.83000 
  • Density:0.948g/cm3 
  • LogP:4.62950 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly) 
Purity/Quality:

99% *data from raw suppliers

GlycidylMyristate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Glycidyl Myristate is formed from monoacylglycerols and are present in edible fats and oils. A potential inhibitor of monoacylglycerol lipase.
Technology Process of Glycidyl Myristate

There total 5 articles about Glycidyl Myristate 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 acetonitrile; at 0 - 20 ℃; for 12.5h; Inert atmosphere;
DOI:10.1002/chem.201904686
Guidance literature:
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 24h; Cooling with ice;
DOI:10.1007/s11746-011-1873-1
Guidance literature:
Multi-step reaction with 2 steps
1: Amberlyst 15 / toluene / 24 h / Reflux
2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 24 h / 20 °C / Cooling with ice
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; toluene;
DOI:10.1007/s11746-011-1873-1
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