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. 2020 Oct 9;61(12):1539–1555. doi: 10.1194/jlr.S120001025

TABLE 2B.

Level-dependent shorthand notation for examples of fatty acids

Subclass Species Levela,b DB-Position Levelc Full Structure Leveld Complete Structure Level (= Common Name)e
Straight-chain FA FA 12:0 Laurate
FA 14:0 Myristate
FA 16:0 Palmitate
FA 16:1 FA 16:1(9) FA 16:1(9Z) Palmitoleate
FA 18:0 Stearate
FA 18:1 FA 18:1(9) FA 18:1(9Z) Oleate
FA 18:1 FA 18:1(11) FA 18:1(11E) trans-Vaccenate
FA 18:2 FA 18:2(9, 12) FA 18:2(9Z,12Z) Linoleate
FA 18:3 FA 18:3(9, 12, 15) FA 18:3(9Z,12Z,15Z) α-Linolenate
FA 18:3 FA 18:3(6, 9, 12) FA 18:3(6Z,9Z,12Z) γ-Linolenate
FA 18:4 FA 18:4(6, 9, 12, 15) FA 18:4(6Z,9Z,12Z,15Z) Stearidonate
FA 20:0 Arachidate
FA 20:3 FA 20:3(8, 11, 14) FA 20:3(8Z,11Z,14Z) dihomo-γ-Linolenate
FA 20:3 FA 20:3(11, 14, 17) FA 20:3(11Z,14Z,17Z)
FA 20:3 FA 20:3(5, 8, 11) FA 20:3(5Z,8Z,11Z) Mead acid
FA 20:4 FA 20:4(5, 8, 11, 14) FA 20:4(5Z,8Z,11Z,14Z) Arachidonate
FA 20:5 FA 20:5(5, 8, 11, 14, 17) FA 20:5(5Z,8Z,11Z,14Z,17Z) Eicosapentaenoate
FA 22:0 Behenate
FA 22:6 FA 22:6(4, 7, 10, 13, 16, 19) FA 22:6(4Z,7Z,10Z,13Z,16Z,19Z) Docosahexaenoate
FA 24:0 Lignocerate
FA 24:1 FA 24:1(15) FA 24:1(15Z) Nervonate
FA 32:5 FA 32:5(14, 17, 20, 23, 26) FA 32:5(14Z,17Z,20Z,23Z,26Z) Dotriacontapentaenoic acid; FA 32:5(n-6)
FA 34:5 FA 34:5 (19, 22, 25, 28, 31) FA 34:5(19Z,22Z,25Z,28Z,31Z) Tetratriacontapentaenoic acid; FA 34:5(n-3)
FA 36:6 FA 36:6(18, 21, 24, 27, 30, 33) FA 36:6(18Z,21Z,24Z,27Z,30Z,33Z) Hexatriacontahexaenoic acid; FA 36:6(n-3)
Fatty acyl ester FA 19:0 FA 18:0;1OMe Methyl stearate
Methyl branched FA 20:0 FA 16:0;3Me,7Me,11Me,15Me FA 16:0;3Me,7Me[R],11Me[R],15Me (Phytanate)
Hydroxy FA 18:0;O FA 18:0;9OH FA 18:0;9OH[S]
Oxo FA 11:1;Ob FA 11:0;9oxo FA 11:0;9oxo
Cyclopropane FA 19:1 FA 19:0;[11-13cy3:0] Lactobacillic acid
Cyclopropene FA 19:2 FA 19:0;[9-11cy3:1(9)] Sterculic acid
Cyclopentene FA 18:3 FA 18:1(6Z);[14-18cy5:1(15)] Gorlic acid
a

Uncharged molecular mass measured by low resolution MS of corresponding m/z from carboxylate anion (electrospray ionization) or molecular ion species (radical cation by EI).

b

Annotation based on the assumption of a straight-chain fatty acyl plus functional groups based on exact mass measurements using a high-resolution mass spectrometer of fatty acyl indicating ion.

c

Positions of DBs determined by independent techniques such as ozonolysis (8) or photochemical derivatization (9).

d

Shorthand notation applies only when exact location and nature of functional group(s) are determined by specific fragment ions obtained by derivatization and GC/MS or specific product ions in a MS/MS experiment.

e

Validated assay is required to employ trivial names that engages appropriate internal standard, proper assessment of signal-to-noise, and a chromatographic based separation of potential isomers (GC or HPLC).