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22,22,22-d3-docosanoic acid

Base Information
  • Chemical Name:22,22,22-d3-docosanoic acid
  • CAS No.:1193721-67-3
  • Molecular Formula:C22H44O2
  • Molecular Weight:343.566
  • Hs Code.:
22,22,22-d<sub>3</sub>-docosanoic acid

Synonyms:

Suppliers and Price of 22,22,22-d3-docosanoic acid
Supply Marketing:
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
  • Medical Isotopes, Inc.
  • Docosanoic-22,22,22-d3Acid
  • 100 mg
  • $ 690.00
  • American Custom Chemicals Corporation
  • DOCOSANOIC-22,22,22-D3 ACID 95.00%
  • 5MG
  • $ 505.90
Total 2 raw suppliers
Chemical Property of 22,22,22-d3-docosanoic acid
Chemical Property:
  • Melting Point:79 - 81°C 
Purity/Quality:

97% *data from raw suppliers

Docosanoic-22,22,22-d3Acid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Docosanoic-22,22,22-d3 Acid can be used to study the neutron diffraction study on basic nanostructure of stratum corneum lipid matrices based on ceramides [EOS] and [AP]
Technology Process of 22,22,22-d3-docosanoic acid

There total 17 articles about 22,22,22-d3-docosanoic acid 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 chromium(VI) oxide; sulfuric acid; In chloroform; acetone; at 0 ℃; for 3h;
DOI:10.1002/jlcr.3443
Guidance literature:
Docosansaeure, D2O;
Guidance literature:
Multi-step reaction with 7 steps
1.1: lithium aluminium tetrahydride / diethyl ether / Reflux
2.1: triethylamine / chloroform / 14 h / 0 - 20 °C
3.1: lithium aluminium deuteride / diethyl ether / Heating
4.1: triphenylphosphine; bromine / dichloromethane / 12 h
5.1: magnesium / tetrahydrofuran / 3 h / 50 °C / Inert atmosphere
5.2: 3 h / -10 - -5 °C / Inert atmosphere
6.1: pyridinium p-toluenesulfonate / methanol / 3 h / Reflux
7.1: sulfuric acid; chromium(VI) oxide / chloroform; acetone / 3 h / 0 °C
With chromium(VI) oxide; lithium aluminium tetrahydride; lithium aluminium deuteride; sulfuric acid; bromine; pyridinium p-toluenesulfonate; magnesium; triethylamine; triphenylphosphine; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; chloroform; acetone; 5.1: |Grignard Reaction / 5.2: |Grignard Reaction;
DOI:10.1002/jlcr.3443
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