Tirzepatide, tested by an independent U.S. lab.
The long fatty acid chain on tirzepatide is the difficult part of the synthesis, and the first thing to go missing when a batch is made badly. A backbone without its side chain still behaves like a peptide on a purity trace, so the percentage can look respectable while the molecule is wrong. What it cannot do is weigh the right amount, which is why identity here is a mass measurement and not an inference from a chromatogram. Every sample is run for intact mass by LC-MS and for purity by HPLC-UV in Elyria, Ohio, and a second analyst checks the work before the certificate is signed. Identity, quantity, and purity are included in the base test. Endotoxin testing, sterility testing, and heavy metals testing are available as optional add-ons.
How a sample becomes
a certificate.
Every tirzepatide sample moves through the same five steps. No shortcuts for rush orders. No unnamed hands in the middle.
Intake.
Your sample arrives. We photograph it, weigh it, log every detail, and assign a tracking number that follows it onto every page.
Prep.
A named analyst prepares the run: dissolutions, dilutions, internal standards. Their initials go in the log.
Run.
HPLC-UV for purity, LC-MS for identity, and quantitative analysis for the amount present, with system-suitability standards bracketing your sample on either side.
Review.
A second analyst reviews the chromatogram independently. Nothing ships with one set of eyes on it.
Sign.
The COA is digitally signed, hashed, and published. Anyone with the link can verify the signature against the raw data.
What we look for in tirzepatide
The whole molecule, not just a peak.
A truncated backbone or an unattached side chain can still produce a clean-looking purity number. Intact mass is what tells you the molecule in the vial is the molecule on the label.
Whether it is tirzepatide at all.
Tirzepatide and semaglutide get confused on labels and in production. They differ by 699.87 daltons on average mass, so one run settles it.
How much is actually in the vial.
Purity and quantity answer different questions. The base test reports both HPLC-UV percent-area purity and the measured quantity in the submitted sample.
Paper you can stake a reputation on.
A signed Certificate of Analysis
Identity, quantity, and purity on one document, signed by the director, not a template stamp.
Method-level transparency
Column, wavelength, ionization mode, and acceptance criteria are stated, not implied.
Public verification
Each COA carries a hash and signature anyone can check at our verify endpoint, on or off our site.