Science-backed · Quality driven
Every vial is tested, logged and traceable.
Transparency and integrity, always. Here is exactly what happens between synthesis and your bench — and how to pull up the record for the lot in your hand.
Batch record lookup
Enter the lot number printed on the vial label (for example KP-RETA-2601) or the product name.
| Lot | Product | Purity | Identity | Method | Tested |
|---|---|---|---|---|---|
| KP-RETA-2601 | Retatrutide 10mg | ≥98% | Confirmed | RP-HPLC + ESI-MS | 2026-01-14 |
| KP-GHK-2602 | GHK-Cu 50mg | ≥98% | Confirmed | RP-HPLC + ESI-MS | 2026-02-03 |
| KP-BAC-2602 | Bacteriostatic Water 3ml | 0.9% benzyl alcohol | Confirmed | Sterility + endotoxin | 2026-02-11 |
Our four-stage process
Step 1
Sourcing
Synthesised by audited partner labs with documented solid-phase peptide synthesis protocols.
Step 2
Identity & purity
Every batch is verified by HPLC for purity and mass spectrometry for identity before release.
Step 3
Cold chain
Lyophilised vials are stored at 2–8°C and shipped insulated so the product arrives as it left.
Step 4
Documentation
A batch certificate accompanies every order, with lot number, assay results and test date.