Quality Assurance Division
Lab Reports & Certificates
Third-party verified. ISO-accredited. Every batch analyzed by HPLC, mass spectrometry, and endotoxin screening before it reaches you.
Avg Purity
ISO 17025 Accredited
COA Rate
Batches Tested
Analytical Methods
Test Methodology
Every compound undergoes a three-tier analytical pipeline before batch release.
HPLC
High-Performance Liquid Chromatography
Separates, identifies, and quantifies each component in a mixture. Our HPLC analysis confirms peptide purity to 0.01% resolution with UV detection at 214nm wavelength.
MS
Mass Spectrometry
Measures the mass-to-charge ratio of ions to confirm molecular identity. Every batch is verified against the theoretical molecular weight with <0.1 Da deviation.
LAL
Endotoxin (LAL) Testing
Limulus Amebocyte Lysate assay detects bacterial endotoxins to accepted analytical sensitivity thresholds. Research-only batches are screened for documentation, transparency, and quality-control review.
Sample Analysis
Certificate of Analysis
Every batch ships with a full COA. Here is what a typical analysis looks like.
Certificate of Analysis
Batch #BPC-26A
Analyzed
2026-01-15
HPLC Chromatogram (214nm)
Recent Batch Purity Results
Document Archive
Latest Analysis Documents
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All compounds are tested by an ISO 17025 accredited third-party laboratory. Reports include HPLC chromatograms, mass spectrometry confirmations, and endotoxin screening results.