Tesamorelin
Analytical results for lot TES10VCS0126 (10 mL vial), third-party tested by AxisPharm, LLC and reported 2026-02-20.
| Assay | Method | Result |
|---|---|---|
| Purity | HPLC-UV (208 nm) | >99.3% |
| Identity | LC-MS (ESI+) | 1286.1 [M+4H], 1029.0 [M+5H] |
| Endotoxin | LAL assay | 0.059 EU/mg |
Lot record
| Lot number | TES10VCS0126 |
|---|---|
| Compound | Tesamorelin |
| Format | 10 mL vial |
| Label claim | 10 mg |
| Measured content | 9.6 mg |
| Expected mass | 5135.78 g/mol |
| Report date | 2026-02-20 |
| Sample received | 2026-02-19 |
| Manufactured | 2026-01 |
| Best before | 2028-01 |
| Manufacture | GMP-compliant peptide manufacturing facility, United States |
| Third-party analysis | AxisPharm, LLC |
| Status | Current — in stock |
Compound
A stabilised 44-residue GHRH analogue carrying an N-terminal hexenoyl modification.
Tesamorelin specification →Other lots of Tesamorelin
Lot-to-lot comparison across releases.
The certificate for this lot
The results above are published in full. The certificate itself is the testing laboratory’s document, and we supply it per batch rather than as a public download — so a certificate can only ever travel with the material it describes. If you hold or are purchasing lot TES10VCS0126, request it and we will send it.
Request the certificate for TES10VCS0126 →All compounds supplied by BioIntegrity are intended strictly for laboratory research and educational use. Not for human or animal consumption. Not for diagnostic, therapeutic, or clinical use. No statement on this website has been evaluated by the Food and Drug Administration. Purchaser affirms that products are acquired solely for legitimate laboratory research and assumes full responsibility for lawful handling, storage, and disposal.