Verification · 6 min read
Purity and Identity Are Not the Same Claim
The most common misreading of a peptide certificate is treating a purity percentage as an answer to 'is this the right compound.' It is not, and the distinction is not pedantic.

Two questions that look like one
Purity asks: of everything in this vial, what proportion is a single component? Identity asks: what is that component?
In ordinary use the two collapse together, because a buyer reading '99% pure semaglutide' reasonably hears both claims at once. Analytically they are independent, and they are established by different measurements. A high purity figure is fully compatible with the wrong molecule, provided the wrong molecule is what is overwhelmingly present.
A sample that is 99% one substance is 99% pure. Whether that substance is the one on the label is a different measurement.
How the two come apart in practice
The cleanest example is a product name that does not fix a chemical identity. TB-500 is sold both as full-length thymosin β-4 and as a short fragment based on the LKKTETQ actin-binding motif. Their molecular weights differ by roughly a factor of five. Each can be manufactured to a high chromatographic purity, and a certificate reporting purity alone cannot tell you which one you received.
The same gap appears with truncated or deletion sequences, where a synthesis has dropped a residue. The product is a peptide, absorbs at the same detection wavelength, and may elute close to the intended compound. If it co-elutes it is not even resolved as a separate peak.
None of this requires anyone to be dishonest. A purity figure can be accurate, reproducible and correctly reported while the identity question has simply never been asked.
What establishes identity
Mass spectrometry is the usual first answer. An observed molecular weight matching the calculated mass for the expected formula is strong evidence that the intended molecule is present, and it is what separates the two TB-500 products immediately.
Intact mass has a known limit: molecules of the same mass are indistinguishable by it. Sequence isomers share a molecular weight, so a mass match does not by itself confirm the order of residues. Where that matters, fragmentation methods read sequence rather than only mass.
Retention time against a characterised reference standard, run under the same method, adds supporting evidence. On its own it is corroborative rather than conclusive.
What a certificate should let you check
A batch identifier, so the document corresponds to material rather than to a product line. A date. The methods used, with enough conditions stated that the purity figure means something. A purity result. A mass result. The name of the laboratory that produced it.
If a certificate carries a purity figure and nothing addressing identity, that is not necessarily a defect in the testing. It is a limit on what the document supports, and it is worth knowing which of the two questions you have an answer to.
Where this site holds a transcribed purity figure it prints it and calls it certified. Where it holds a published certificate without one, it says so rather than substituting the supplier's specification. Where there is no certificate, the figure shown is the supplier specification and is labelled as such on the same line.
Common questions
What is the difference between purity and identity in peptide testing?
Purity is the proportion of a sample that is a single component, typically measured by HPLC peak area. Identity is what that component actually is, typically established by mass spectrometry. They are independent: a sample can be highly pure and still not be the labelled compound.
Can a certificate of analysis show high purity for the wrong compound?
Yes, and without any dishonesty. Purity describes proportion, so a vial that is overwhelmingly one substance yields a high purity figure regardless of which substance it is. Establishing that it is the labelled compound requires a separate determination, usually molecular weight by mass spectrometry.
Why do two suppliers' TB-500 have different molecular weights?
Because TB-500 is a product name rather than a chemical identity. Some suppliers ship full-length thymosin β-4, near 4963 g/mol; others ship a short fragment based on the LKKTETQ actin-binding motif, near 889 g/mol. Both can be high purity. The molecular weight on the certificate is what distinguishes them.
Does a matching molecular weight prove the sequence is correct?
Not on its own. Intact mass cannot separate molecules that weigh the same, including sequence isomers. A mass match is strong evidence the intended molecule is present; confirming the order of residues requires fragmentation methods such as MS/MS.
All products sold on this website are intended for research and identification purposes only. These products are not intended for human dosing, injection, or ingestion.

