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Determination of tetrabutylammonium chloride

Discussions about GC-MS, LC-MS, LC-FTIR, and other "coupled" analytical techniques.

3 posts Page 1 of 1
Hi all,

I have a need to determine the level of TBAC in a material.

For an ion pairing agent the compound seems well retained on a C18 column (standard ACN:Water 0.03%TFA) and is easily detected by LCMS (obviously as the quat ammonium ion).

However, the RSD for 6 replicate injection is ~20% and the Linearity has an R2 = 0.8164. A spiked sample recovered only ~70% of the TBAC.

I've also tried it under 0.1% formic acid conditions but observed the same results.

This instrument produces acceptable results for other compounds - so any idea as to the reason for this compound specific variability?

Many thanks in advance,

Serp.
Hi all,

I have a need to determine the level of TBAC in a material.

For an ion pairing agent the compound seems well retained on a C18 column (standard ACN:Water 0.03%TFA) and is easily detected by LCMS (obviously as the quat ammonium ion).

However, the RSD for 6 replicate injection is ~20% and the Linearity has an R2 = 0.8164. A spiked sample recovered only ~70% of the TBAC.

I've also tried it under 0.1% formic acid conditions but observed the same results.

This instrument produces acceptable results for other compounds - so any idea as to the reason for this compound specific variability?

Many thanks in advance,

Serp.
Given the immense difficulty in completely removing an IP reagent from a C18 column which has been used in IP chromatography, I am not surprised at you results.


Have you tried using less non-polar stationary phases, they may improve your results.
Good judgment comes from bad experience, and a lot of that comes from bad judgment.

HILIC column may work better
3 posts Page 1 of 1

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