Hi everyone!

I am doing a derivatization reaction for conversion of formaldehye into a more friendly GC analyte, diethoxymethane. The reaction is done in a 10 mL headspace vial, and a sample of formaldehyde is exposed to excess of pure ethanol with p-toluenesulfonic acid as a catalyst. The vial is heated, agitated and injection done after ~20 minutes of equlibration.

Here is where I am seing some odd behavior - a 1000 ppm standard of the pure derivative (diethoxymethane) yields a much lower area in comparison to a 1000 ppm standard of formaldehyde that undergoes the derivatization.

I am new at derivatization, so I was wondering if this is something normal?

Thanks!

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