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Medutest (revision 20)

Old revision·00:43, 12 May 2025·ChromCleanupCass

This is an old revision of this page, as it stood at 00:43, 12 May 2025, saved by ChromCleanupCass with the summary correct the description of the sampling procedure. It may differ substantially from the current revision, and any error it contains may since have been corrected.
MedutestIndependent testing service
CERTIFICATE OF ANALYSISLot SM-2604-1182026-04-11AppearanceWhite powderPassPurity (HPLC)99.12 %PassPeptide content82.4 %PassWater (KF)4.1 %PassTFA0.42 %PassEndotoxin<0.5 EU/mgPassQA sign-off
TypeAnalytical testing service
Commissioned byThe submitter
OutputReport on the submitted sample
Testing service infobox · conventions

Medutest is an independent testing service that analyses peptide samples submitted by purchasers and reports the results to the submitter. It is one of the four testing and review services referred to throughout this wiki, alongside Janoshik Analytical, PeptideMeter and VendorInvestigate.[1]

Like any third-party analysis, a Medutest report is evidence about the material that reached the laboratory. Whether it can be extended to the lot from which that material came depends on how the sample was drawn, and whether it can be extended to a supplier depends on the number of lots examined and the period over which they were sampled.[1]

Reports referenced on this wiki are those submitted by contributors. They are a self-selected sample and are not a survey of the market.

What a submitted report establishes

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The determinations most often present in reports submitted to this wiki are chromatographic purity by area percent and, where commissioned, identity confirmation by mass. Some submissions include a peptide content figure; most do not.[2]

The distinction matters more than it is usually given credit for. Purity is an area-normalised figure describing the composition of what was injected; content is a mass figure describing how much peptide is present. A material can be 99% pure and 60% peptide by mass, the balance being water, counterion and residual solvent — see Trifluoroacetate counterion and Loss on drying. Those two figures answer different questions and neither substitutes for the other.

Where a report and a supplier certificate both exist for a lot, comparison is only meaningful if the methods are comparable. Two purity figures obtained on different gradients are not directly comparable, and a difference of a few tenths of a percentage point is within ordinary method repeatability.[2][3]

Use of results on this wiki

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This wiki records what submitted documents state. It does not commission testing, does not hold samples, and does not verify that a submitted document is genuine beyond ordinary editorial scrutiny — a limitation described at Test report forgery.[1]

Community submissions are aggregated in a tally that is explicitly labelled as self-reported. The tally counts submissions, not lots and not purchases, and a supplier with more submissions is not thereby better characterised in any statistical sense: it may simply have more customers who report.

Where a submission is used to support a statement in an article, the statement is attributed to the submission rather than presented as an established fact about the supplier. This is a requirement of the sourcing guidelines rather than a courtesy.

See also

References

  1. ^ a b c PeptidePedia Wiki community test-report tally, 2024–2026 (self-reported; see Project:Sourcing guidelines).
  2. ^ a b United States Pharmacopeia, General Chapter <1503>, Quality Attributes of Synthetic Peptide Drug Substances.
  3. ^ United States Pharmacopeia, General Chapter <621>, Chromatography.