Science without compromise.
Our synthesis and testing methodology is built on pharmaceutical-grade standards. Every decision — from sourcing to shipment — is governed by a single question: is this the most rigorous approach possible?
From synthesis to shipment.
Every compound follows the same rigorous 5-step process — no exceptions, no shortcuts.
Raw Material Sourcing
We source only pharmaceutical-grade amino acids and reagents from verified suppliers. Every incoming material is tested for identity and purity before entering production.
Solid-Phase Peptide Synthesis
Compounds are synthesised using automated SPPS technology under strictly controlled temperature and humidity conditions in our GMP-certified facility.
Purification
Each batch undergoes reverse-phase HPLC purification to remove impurities and achieve target purity levels of 99%+. Purification parameters are logged for every run.
Third-Party Testing
Before any batch is released, samples are sent to an independent accredited laboratory for verification. We do not release batches that fail to meet our purity specification.
Packaging & Dispatch
Compounds are lyophilised, sealed under nitrogen, and labelled with full batch traceability data. Cold-chain packaging is used for temperature-sensitive compounds.
Every batch. Every time.
We apply six independent testing protocols to every production batch. No sampling — every batch is tested in full.
Mass Spectrometry
Confirms molecular identity and detects any structural anomalies at the molecular level. Required for every compound, every batch.
HPLC Purity Analysis
High-performance liquid chromatography measures purity concentration. Minimum threshold: 99.0%. Batches below this are not released.
Amino Acid Analysis
Verifies the exact amino acid composition of each peptide compound against the target sequence specification.
Endotoxin Check
LAL testing confirms endotoxin levels are within acceptable limits for research-grade compounds, minimising contamination risk.
Microbial Testing
Each batch is screened for microbial contamination including bacteria, yeast, and mould before packaging and dispatch.
Water Content (KF)
Karl Fischer titration determines residual moisture content in lyophilised compounds, ensuring product stability and shelf life.
Certificate of Analysis — for every batch.
Every compound ships with a full Certificate of Analysis from an independent accredited laboratory. The COA documents identity, purity, concentration, and test results — permanently accessible in our documentation library.
- Independent third-party laboratory
- Molecular identity confirmation (MS)
- Purity percentage (HPLC)
- Batch number and production date
- Expiry and storage conditions
- Technician sign-off and accreditation