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c/hplc·posted 4 days ago by u/mass_spec_maggie

[Lab] LC-MS confirmed identity but the UV purity is 94%. now what

Lab Clean Column ×4

Research peptide, not a GLP-1, from a vendor I will not name because this is a methodology question rather than a vendor post.

MS confirms the expected molecular mass and the fragmentation is consistent with the sequence. So it is the right molecule. UV purity integrates to 94.1%, with a single impurity at 3.2% and the rest scattered.

So: correct identity, mediocre purity, one dominant impurity. How do people weigh that? Genuinely asking, because I keep going back and forth.

1,200 up / 381 down76% upvoted27 commentsid 1hly5g25 Jul 2026

27 comments

12 in this archive, depth 6

best — the order this archive was captured in

u/sig_figs_samMOD276 points·4 days ago

The 3.2% single impurity is the whole question and MS can probably tell you what it is. If it is a related substance — a truncation, an oxidation, a des-amido — that is a synthesis and purification story and it is disappointing rather than alarming.

If it is unrelated, that is a different conversation. Can you get a mass on that peak?

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u/mass_spec_maggieOPMS187 points·3 days ago·edited

i can and i should have. edit next day: it is +16 on the parent mass. so an oxidation product, almost certainly methionine, and almost certainly a storage or handling artefact rather than a synthesis failure.

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u/sequence_checkerresearch peptides154 points·3 days ago

+16 with a met in the sequence is about as unambiguous as this gets. which means the material was made properly and then sat somewhere with air.

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u/coldchain_karencold chain132 points·3 days ago

and oxidation is one of the routes that does not need much water, so it is one of the few things that does progress in a dry vial over long enough.

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u/mass_spec_maggieOPMS118 points·3 days ago

so the practical read is: correct molecule, honest vendor, old vial. that is a much more actionable conclusion than "94% bad".

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u/purity_pedantanalytical96 points·3 days ago

and this is why identity plus profile beats a single purity figure. 94% tells you nothing about which of six stories you are in.

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u/analog_alphabet121 points·4 days ago

for anything outside the GLP-1s i would put identity first and purity second every time. the naming mess in the research-peptide supply chain means "is this the right thing" is a live question.

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u/quant_not_qual84 points·4 days ago

and neither number tells you how much peptide is in the vial. three questions, three assays, one document.

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u/rui_only_ro58 points·4 days ago

research use only reminder since this is not a GLP-1: handling and analysis discussion is fine, protocols are not.

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u/devils_advocate_d-13 points·4 days ago

94% is 94%. all this analysis is a long way of avoiding the word bad.

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u/mass_spec_maggieOPMS108 points·3 days ago

a 94% that is one identified oxidation product on an old vial and a 94% that is six unknown peaks are not the same material. that is not avoidance, it is the actual difference.

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[deleted]3 points·4 days ago

[deleted]

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