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

Base Information

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

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:

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 5 raw suppliers

Chemical Property of Docosa-7,10,13,16-tetraenoic acid

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:: 99% ^*data from raw suppliers

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:

Reference yield:

: ((5Z,8Z,11Z,14Z)-2-Icosa-5,8,11,14-tetraenyl)-malonic acid

: 2091-25-0,28874-58-0
adrenic acid

Guidance literature:: With hydrogenchloride; In diethylene glycol dimethyl ether; at 120 ℃; for 1h; Yield given;

Reference yield:

: 2566-89-4
methyl arachidonate

: 2091-25-0,28874-58-0
adrenic acid

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;

Reference yield:

: 13487-46-2
arachidonyl alcohol

: 2091-25-0,28874-58-0
adrenic acid

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;