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Advice on quantification with hexadecane

Discussions about GC and other "gas phase" separation techniques.

4 posts Page 1 of 1
Currently, I'm using a GC-MS with a HP-5 column to quantify phenol and cyclohexanol which does a good job with quantification in methylene chloride solvent by itself. I am running reactions in hexadecane which is not a good solvent for phenol or cyclohexanol and am using toluene as a co-solvent, but I am having issues with injection repeatability on 75% of my samples. The liner has been changed out and so has the inlet septum. The column is free of obstruction. I have tried to run at a higher inlet temp (310 deg C), but the signal of the low boiling pt components is bad. Is there a way I can get good quantification of phenol and cyclohexanol using the GC? Will I have to use a solvent that is immiscible in hexdecane for quantification? Would LC be a better choice?

Thanks for any suggestions.
Would LC be a better choice?
No, I think GC is a better choice. If you "must" have hexadecane in your matrix, if me I'd try diluting/disssolving all in DMF, keep your column type as it is.

We've used hexadecane successfully as solvent when assaying high-boiling paraffins.
Would LC be a better choice?
No, I think GC is a better choice. If you "must" have hexadecane in your matrix, if me I'd try diluting/disssolving all in DMF, keep your column type as it is.

We've used hexadecane successfully as solvent when assaying high-boiling paraffins.

So you are inferring that Hexadecane will cause issue with quantification?
So you are inferring that Hexadecane will cause issue with quantification?
No.
4 posts Page 1 of 1

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