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Docosa-7,10,13,16-tetraenoic acid

Base Information Edit
  • Chemical Name:Docosa-7,10,13,16-tetraenoic acid
  • CAS No.:2091-25-0
  • Molecular Formula:C22H36O2
  • Molecular Weight:332.527
  • Hs Code.:2916190090
  • DSSTox Substance ID:DTXSID60862828
  • Mol file:2091-25-0.mol
Docosa-7,10,13,16-tetraenoic acid

Synonyms:7,10,13,16-docosatetraenoic acid;adrenic acid;adrenic acid, (Z)-isomer

Suppliers and Price of Docosa-7,10,13,16-tetraenoic acid
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 1 raw suppliers
Chemical Property of Docosa-7,10,13,16-tetraenoic acid Edit
Chemical Property:
  • Vapor Pressure:5.94E-09mmHg at 25°C 
  • Boiling Point:439.5°Cat760mmHg 
  • PKA:4.77±0.10(Predicted) 
  • Flash Point:336.2°C 
  • PSA:37.30000 
  • Density:0.921g/cm3 
  • LogP:6.99690 
  • XLogP3:7.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:16
  • Exact Mass:332.271530387
  • Heavy Atom Count:24
  • Complexity:389
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCCCCC=CCC=CCC=CCC=CCCCCCC(=O)O
Technology Process of Docosa-7,10,13,16-tetraenoic acid

There total 6 articles about Docosa-7,10,13,16-tetraenoic 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 hydrogenchloride; In diethylene glycol dimethyl ether; at 120 ℃; for 1h; Yield given;
Guidance literature:
Multi-step reaction with 5 steps
1: 65 percent / LiAlH4 / diethyl ether / 3 h / Ambient temperature
2: 82 percent / PPh3*Br2 / acetonitrile
3: 1.) Na / 1.)diglyme 2.) diglyme 140 deg C, 2h
4: 40percent aq NaOH / H2O; ethanol / 4 h / Ambient temperature
5: 1.5 M HCl / bis-(2-methoxy-ethyl) ether / 1 h / 120 °C
With hydrogenchloride; sodium hydroxide; lithium aluminium tetrahydride; sodium; triphenylphosphine dibromide 1:1 addition complex; In diethyl ether; ethanol; diethylene glycol dimethyl ether; water; acetonitrile;
Guidance literature:
Multi-step reaction with 4 steps
1: 82 percent / PPh3*Br2 / acetonitrile
2: 1.) Na / 1.)diglyme 2.) diglyme 140 deg C, 2h
3: 40percent aq NaOH / H2O; ethanol / 4 h / Ambient temperature
4: 1.5 M HCl / bis-(2-methoxy-ethyl) ether / 1 h / 120 °C
With hydrogenchloride; sodium hydroxide; sodium; triphenylphosphine dibromide 1:1 addition complex; In ethanol; diethylene glycol dimethyl ether; water; acetonitrile;
Refernces Edit
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