vialroom

#coa-reading 2025-11-16

Sunday39 messages9 participantstimes are UTC
Highlights from this day
  • net_peptide — a lab that reports "greater than 98%" rather than a number is telling you they did not integrate carefully 10:18
  • reship_rita — update from 9 months ago: started asking every supplier for water content and about half now include it 11:47
  • customs_owl — two certificates from the same supplier have an identical chromatogram, is that normal 15:39
  • HPLC_Hank — does purity by hplc at one wavelength miss things 16:20
  • HPLC_Hank — i was wrong about this for a year: area percent under-reports nothing, it just answers a different question than assay does 16:23

not detected means nothing

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NP

sterility and endotoxin are separate tests and almost nobody runs either on research material

NP

the certificate from WWB is the one i use to teach this because it actually has a populated impurity table

a lab that reports "greater than 98%" rather than a number is telling you they did not integrate carefully

💀11👀12🧊13

one decimal versus two is usually just house style, not precision

RR

purity is what fraction of the contents is the target. assay is how many mg are actually there. different questions

CO

my 10mg vial weighed more than 10mg of powder, is the certificate lying

RR

tfa or acetate, how do i tell from the paperwork

fridge-temps.csv
103 rows · not retained in the public archive
CO

tfa counterion runs higher by mass than acetate. if the certificate does not say, you cannot do the mass balance
if the certificate date precedes the lot date, ask. sometimes it is sloppiness and sometimes it is not

RR

update from 9 months ago: started asking every supplier for water content and about half now include it

peak   RRT    area%    note
  1   0.42     0.31    solvent front
  2   0.88     0.44    related substance
  3   1.00    98.72    main
  4   1.14     0.53    related substance
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EE

gross mass on a jewellery scale plus the water content is enough to catch most underfills

1
CO

the three way match is vial, certificate, invoice. if all three agree you have something, ill dig out the number

single wavelength detection can miss a co-eluting impurity that does not absorb there

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EE

retention time shifts between runs are normal. relative retention time is the number to compare

EE

net peptide is gross mass minus water minus counterion. that is why 11.4mg of powder can be a correct 10mg vial

i keep every certificate in a dated folder and compare them. two suppliers had not changed their template since 2019
retention time shifts between runs are normal. relative retention time is the number to compare

whats the minimum a certificate has to have before you take it seriously

whats the related substances table actually telling me

P2

the paperwork can be perfect and the vial can still be light. weigh it

VB

Reminder for customs_owl: dose day is today. Set 7 days ago.

EE

no lot no certificate

peak   RRT    area%    note
  1   0.42     0.31    solvent front
  2   0.88     0.44    related substance
  3   1.00    98.72    main
  4   1.14     0.53    related substance
HH

coming back after 13 months, has the pinned reading guide changed

EE

i asked GGPeps for the method and they sent it. that alone put them ahead of most, i could be wrong

EE

no lot number, no certificate. a document you cannot tie to the vial in your hand is decoration

HH

does purity by hplc at one wavelength miss things

🎉15❤️8

i was wrong about this for a year: area percent under-reports nothing, it just answers a different question than assay does

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EE

right so is endotoxin ever tested on research material

lot-log.csv
439 rows · not retained in the public archive

thats the counterion