2091-25-0

Basic information

• Product Name: 7,10,13,16-Docosatetraenoic acid
• Synonyms: 7,10,13,16-Docosatetraenoic acid
• CAS NO: 2091-25-0
• Molecular Formula: C22H36O2
• Molecular Weight: 332.52
• Mol File: 2091-25-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 439.5°Cat760mmHg
• Flash Point: 336.2°C
• Appearance: /
• Density: 0.921g/cm³
• Vapor Pressure: 5.94E-09mmHg at 25°C
• Refractive Index: 1.498
• PKA: 4.77±0.10(Predicted)
• CAS DataBase Reference: 7,10,13,16-Docosatetraenoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 7,10,13,16-Docosatetraenoic acid(2091-25-0)
• EPA Substance Registry System: 7,10,13,16-Docosatetraenoic acid(2091-25-0)

Safety Data

• Hazardous Substances Data: 2091-25-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C22H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h6-7,9-10,12-13,15-16H,2-5,8,11,14,17-21H2,1H3,(H,23,24)

Upstream product

• 2566-89-4 methyl arachidonate 
• 339570-70-6 ((5Z,8Z,11Z,14Z)-2-Icosa-5,8,11,14-tetraenyl)-malonic acid diethyl ester 
• 13487-46-2 arachidonyl alcohol 
• 108803-63-0 (5Z,8Z,11Z,14Z)-1-bromoeicosa-5,8,11,14-tetraene 

Downstream Products

• 150314-35-5 docosatetraenoyl ethanolamide 

Relevant articles and documents

Synthesis of C2-elongated polyunsaturated fatty acids

The synthesis by a modified malonic ester procedure of C2-elongated polyunsaturated fatty acids from their natural precursors was described. Using the suggested Scheme 1, (7Z,11Z,14Z)-7,11,14-eicosatrienoic, (8Z,11Z,14Z,17Z)-8,11,14,17-eicosatetraenoic, (5Z,8Z,11Z,14Z,17Z)-5,8,11,14,17-eicosapentaenoic, (8Z,11Z,14Z,17Z)-8,11,14,17-docosatetraenoic, (7Z,10Z,13Z,16Z,19Z)-7,10,13,16,19-docosapentaenoic, and (6Z,9Z,12Z,15Z,18Z,21Z)-6,9,12,15,18,21-tetracosahexaenoic acids were synthesized. Their structures were confirmed by GC, UV, and MS data, which coincided with those of natural compounds. The target compounds were shown to be free from by-products, which could result from Z-E isomerization or migration of double bonds. The overall yields of the four-step synthesis of C2-elongated polyenoic acids were 25-30%.