Difference between revisions of "Fatty Acid Methyl Esters"

From MC Chem Wiki
Jump to navigation Jump to search
Line 3: Line 3:
 
[[File:2021-04-13 (1).png|400px]]
 
[[File:2021-04-13 (1).png|400px]]
  
[[File:2021-04-13 (2).png|400px]]
+
[[File:2021-04-13 (2).png|400px|center]]
  
[[File:2021-04-13 (3).png|400px]]
+
[[File:2021-04-13 (3).png|400px|right]]
  
 
==Significance of Fatty Acid Methyl Esters==
 
==Significance of Fatty Acid Methyl Esters==

Revision as of 02:36, 14 April 2021

Background Information

2021-04-13 (1).png

2021-04-13 (2).png
2021-04-13 (3).png

Significance of Fatty Acid Methyl Esters

Transesterification

2021-04-13.png


Image . This reaction is known as transesterification. The methyl from the methanol group is added to the carboxylic acid of the fatty acid to create a fatty acid methyl ester.

Sample Preparation

  • Combined 200 ul of the sample with 40 ul of anhydrous methanol into a microcentrifuge tube
  • Added 4.3 ul of 5 M KOH to the top methanol layer (catalyst)
  • Sonicated the tubes in an ultrasonic bath for 30 minutes
  • Added 200 ul of 0.1 M acetic acid (neutralize the base catalyst)
  • Centrifuged the solution at 6,000 rpm for 5 minutes
  • Transferred 40 ul of the top layer to a GC vial and diluted with pentane

GC-MS Analysis

Data