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Featured Application: 3-MCPD and Glycidyl Esters on Rxi-17Sil MS

Faster GC-MS Analysis of 3-MCPD and Glycidyl Esters in Edible Oils


  • Meet AOCS Cd 29c-13 method requirements with optimized GC conditions.
  • Use split injection to decrease analysis time by 8 min and reduce damage from derivatization reagents.
  • Gain flexibility: use either a PTV or a split/splitless inlet.

Fatty acid esters of 3-chloropropane-1,2,-diol (3-MCPD) and glycidyl esters in edible oils are contaminants that form during refining processes. When ingested, these compounds release free MCPD and glycidol, which are considered potentially carcinogenic and/or genotoxic. The most common analytical approach is an indirect method where esters in the sample are hydrolyzed, further derivatized, and then analyzed by GC-MS. Methods such as AOCS Cd 29c-13—or its international (ISO 18363-1) or national (DGF C-VI 18 (10)) equivalents—are routinely used for this analysis. During the sample preparation process, free glycidol coverts to 3-MCPD under acidic conditions and is then analyzed together with the directly formed 3-MCPD. The chromatographic method calls for a PTV inlet operated in splitless mode, which necessitates a low initial oven temperature (85 ˚C) and solvent focusing to maintain narrow, symmetrical peaks, especially for early eluting compounds. After several temperature gradients, the final analysis time (as published in AOCS Cd 29c-13) is 24.8 minutes.

In order to provide labs with a less time-consuming method for the analysis of 3-MCPD and glycidyl esters, we optimized the AOCS Cd 29c-13 sample introduction technique and temperature program. First, we switched to split injection because it reduces the amount of derivatization reagent that enters the system; this is gentler on the column and MS and can reduce maintenance frequency and replacement costs. Also, because sample transfer from the inlet to the column is much faster with split injection compared to splitless, there is less need for solvent focusing and the initial oven temperature can be much higher. Raising the starting oven temperature to 120 ˚C produced sharp peaks and, even with a 10:1 split ratio, suitable detection limits were achieved. Doubling the first temperature ramp rate from 6 ˚C/min to 12 ˚C/min also sped up the analysis significantly without any negative effects. A higher final oven temperature was also used in order to more effectively remove higher molecular weight contaminants from the column. The optimized method shown here saved 8 minutes compared to the published AOCS Cd 29c-13 analysis time and performed well when tested using both PTV and dedicated split/splitless inlets, providing both faster analysis times and greater flexibility for labs analyzing 3-MCPD and glycidyl esters in edible oils.


PeakstR (min)Conc.
(µg/g)
1.3-MCPD-d5 PBA derivative5.9371.81
2.3-MCPD PBA derivative5.9772.94
3-Monochloropropane-1,2-Diol (3-MCPD) Esters in Olive Oil on Rxi-17Sil MS
GC_FS0566
ColumnRxi-17Sil MS, 30 m, 0.25 mm ID, 0.25 µm (cat.# 14123)
SampleExtracted olive oil
Diluent:Isooctane
Injection
Inj. Vol.:1 µL split (split ratio 10:1)
Liner:Topaz 4.0 mm ID Precision inlet liner w/wool (cat.# 23305)
Inj. Temp.:280 °C
Oven
Oven Temp.:120 °C (hold 0.5 min) to 180 °C at 12 °C/min to 330 °C at 25 °C/min (hold 5 min)
Carrier GasHe, constant flow
Flow Rate:1.4 mL/min
DetectorMS
Mode:SIM
SIM Program:147, 150, 196, 201 m/z, 50 ms dwell
Transfer Line Temp.:320 °C
Analyzer Type:Quadrupole
Source Temp.:230 °C
Quad Temp.:150 °C
InstrumentAgilent 7890A GC & 5975C MSD
NotesThe olive oil sample was spiked with 3-MCPD-d5 ester and prepared according to AOCS method Cd 29c-13.

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