vialroom

#coa-reading 2026-06-16

Tuesday47 messages11 participantstimes are UTC
Highlights from this day
  • abdo_two_inch — purity is what fraction of the contents is the target. assay is how many mg are actually there. different questions 14:44
  • assay_not_purity — the certificate from MKM is the one i use to teach this because it actually has a populated impurity table 16:09
  • taipei_tare — nobody can authenticate a certificate from a scan. you authenticate the material by testing it yourself 16:10
AP

update from 13 months ago: started asking every supplier for water content and about half now include it

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AN

i keep every certificate in a dated folder and compare them. two suppliers had not changed their template since 2019

AT

a vial can be 99.4% pure and hold 8.1mg of a 10mg label. both numbers are true and only one of them is the one you care about

peptidemeter-summary-f-1330.pdf
2 pages · 101 KB · not retained in the public archive

unrelated but does anyone keep a folder of certificates to compare over time

PS

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

a supplier certificate on its own is a starting point, not evidence. that is the whole reason the verification channel exists

PT

the related substances table is the interesting part. a row of "not detected" means they did not look hard, i have it written down somewhere

[edited]
AT

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

📈6🙏12
AT

the retention time on this one is different from the last lot, problem

AN

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

VB

Channel stats, last 30 days: 85 messages from 9 members.

CC

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

CC

genuine question if the certificate date precedes the lot date, ask. sometimes it is sloppiness and sometimes it is not
a vial can be 99.4% pure and hold 8.1mg of a 10mg label. both numbers are true and only one of them is the one you care about

test it yourself

AN

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

coa-b-0329.pdf
1 page · 97 KB · not retained in the public archive
TT

nobody can authenticate a certificate from a scan. you authenticate the material by testing it yourself

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CO

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

if you only read one line on a certificate, read the lot number. if you read two, read the assay
the certificate from Homopeptide is the one i use to teach this because it actually has a populated impurity table

[edited]
CO

tfa counterion runs higher by mass than acetate. if the certificate does not say, you cannot do the mass balance

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CO

sterility and endotoxin are separate tests and almost nobody runs either on research material
single wavelength detection can miss a co-eluting impurity that does not absorb there

water content is why an honest 10mg vial assays at 9.1. karl fischer titration, and most certificates omit it

[edited]
IO

mixed fonts and inconsistent kerning in one document is worth a second look

TT

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

TT

residual solvents matter more than people think for anything that went through a lot of purification steps

does anyone actually check the residual solvents section

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does purity by hplc at one wavelength miss things

IO

i asked FGP for the method and they sent it. that alone put them ahead of most

VB

Channel stats, last 30 days: 137 messages from 56 members.

IO

why do some certificates report to one decimal and some to two