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#hplc-massspec 2025-09-06

Saturday22 messages7 participantstimes are UTC
Highlights from this day
  • non_scale_win — baseline drift on a gradient is normal. baseline drift on an isocratic hold is your column if the lab reports area percent without stating the wavelength, the number… 19:53
  • peak_split — i have had a lot where the mass was exactly right and the purity was 96.8. wrong question, right answer 20:33
  • peak_split — oxidation is about plus 15.99 Da and is usually methionine or tryptophan, for what its worth 20:56
  • non_scale_win — shallow gradients hide related substances behind the main peak. a steeper one separates and looks worse, honestly 21:15
HH

if the lab reports area percent without stating the wavelength, the number is less useful than it looks

VB

Digest for the week of 2025-04-13 has been published.

PS

monoisotopic and average diverge more the bigger the molecule. say which one you are quoting
a warm transit can put a visible degradant peak on a chromatogram. that is what 7 days at ambient does

within inter-lab range

HH

retention time is a hint, not a fingerprint. two different peptides can co-elute perfectly happily

a dimer usually shows up late and at roughly double the mass. the chromatogram alone will not tell you

PS

i have had a lot where the mass was exactly right and the purity was 96.8. wrong question, right answer

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how would a truncation sequence show up

FT

i asked VendorInvestigate for the raw trace and they sent it. that is the right answer to that question

semaglutide is about 4113.6 Da. [M+2H]2+ lands near 2057.8, [M+3H]3+ near 1372.2

plus 0.98 is deamidation

PS

oxidation is about plus 15.99 Da and is usually methionine or tryptophan, for what its worth

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NS

shallow gradients hide related substances behind the main peak. a steeper one separates and looks worse, honestly

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