MESO "Specialized" Testing Group Fund

Request the "raw data" for HPLC data so we have it for posterity. Other peaks on the chromatogram? Surely a couple of the ones seen on the GC trace should show up (gonane cores)?

Since we are finding free "hormone" on some of the GC data where is the fatty acid if the ester is thermally cracking in the GC? Hint: it ain't.
 
yeah but there is a mass spectrometry available for hplc as far as I’m aware, and previously Jano has said they include it by default now for all hplc.
 
yeah but there is a mass spectrometry available for hplc as far as I’m aware, and previously Jano has said they include it by default now for all hplc.
His default detector is UV-VIS IIRC for standard UHPLC screenings. MS is an option but not standard.

 
@janoshik I thought I read somewhere that you include MS with all HPLC or is that only for specific tests?

Also, could LC-MS quantitatively identify some of these closely related substances maybe in these steroid samples or in any way be helpful to us here?
 
His default detector is UV-VIS IIRC for standard UHPLC screenings. MS is an option but not standard.

Big difference! without ms and only uv vis we cant identify unknown peaks! and it overestimates the purity.

with the hplc-ms we can identify each peak with the mol weight and match it to database.

how much extra did you say the ms option cost?
 
Big difference! without ms and only uv vis we cant identify unknown peaks! and it overestimates the purity.

with the hplc-ms we can identify each peak with the mol weight and match it to database.

how much extra did you say the ms option cost?
I didn't. It is on here somewhere.
 

Here is the standard method: HPLC-DAD.
 
Big difference! without ms and only uv vis we cant identify unknown peaks! and it overestimates the purity.

with the hplc-ms we can identify each peak with the mol weight and match it to database.

how much extra did you say the ms option cost?



See front page. Not sure it is set up for AAS. Above he says it is an option. Might be an interesting angle. Would need to consult with their team.

Code:
https://janoshik.com/pricing/
 
gcms is defiently better for aas. only reason to run hplc ms is just for overall cost savings instead of running hplc-dad + gc-ms
If you want gnat's ass accuracy and ID of everything you need GCMS plus derivatization. We are here spinning our wheels between the HPLC and GCMS data. Co-eluting HPLC peaks? HPLC overestimating purity? Hard for me to reconcile the GCMS data with the HPLC purity data. Volatility and ionization of each component, etc. All over the internet LMAO.

Risk of false positive purity with current HPLC setup?
 
gcms is defiently better for aas. only reason to run hplc ms is just for overall cost savings instead of running hplc-dad + gc-ms

Issue is that GCMS wont give you purity% to brew oils.
Non-volatile stuff also won't turn up, so even if you have a nice GCMS, you might get low purity% due to non-volatile crap contamination.
 

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