Certificate of Analysis
“WOLVERINE” – BPC-157/TB-500
Batch B1326014 · Tested April 13, 2026 5/5mg
✓ Third-Party Lab Tested
Independent laboratory testing confirms purity, composition, and endotoxin safety per USP <85> standards. Results apply only to this specific batch; for research use only.
Sample Summary
Identification and intake details for this tested batch.
Product
“WOLVERINE” – BPC-157/TB-500
Volume
5/5mg
Batch / Lot
B1326014
Accession #
2604130351
Test Date
April 13, 2026
Appearance
White Lyophilized Powder
Identity
Confirmed via LC-MS
Purity Analysis
HPLC-UV
Purity (HPLC-UV)
99.35%
Identity (LC-MS)
BPC-157/TB-500
Net Peptide Content
BPC-157 – 6.11 mg, TB-500 – 4.85 mg
Test Method
HPLC-UV
What this test measures
High-performance liquid chromatography with UV detection separates the peptide from related impurities and quantifies each fraction. Mass spectrometry confirms molecular identity by measuring the exact mass-to-charge ratio.
Endotoxin Analysis
Limulus Amebocyte Lysate assay in accordance with USP <85>.
Result
✓ Cleared (below threshold)
Sensitivity
≤0.05 EU/mL
What this test measures
The LAL assay detects bacterial endotoxin at the reporting threshold shown. Both replicates must be below the threshold established by USP Chapter <85> to clear. For research-grade material handling only.
Full Certificate PDF
Signed laboratory-issued PDF with chromatogram and mass confirmation plots.
Test History for “WOLVERINE” – BPC-157/TB-500
7 independent lab tests on file for this product.
99.31%
Avg Purity · 7 batches
98.61% – 99.85%
Range
1 on file
Endotoxin Tests
99.35%
Batch B1326014 · 5/5mg
Apr 13, 2026 · Purity + Endotoxin
99.69%
Batch B0526 · 5/5mg
Mar 20, 2026 · Purity
99.85%
Batch B0526 · 5/5mg
Feb 18, 2026 · Purity
99.37%
Batch 14CBF · 5/5mg
Jan 22, 2026 · Purity
99.01%
Batch 14CBF · 5/5mg
Jan 7, 2026 · Purity
98.61%
Batch 14HBE · 5/5mg
Nov 12, 2025 · Purity
99.30%
Batch 14HBE · 5/5mg
Aug 25, 2025 · Purity
Frequently Asked Questions
Quick references for what each test means.
What is HPLC-UV purity testing?
High-Performance Liquid Chromatography (HPLC) separates the peptide from related impurities based on how strongly each molecule interacts with a chromatographic column. A UV detector quantifies each separated fraction, and the total peptide peak area divided by all peaks yields the purity percentage.
What does LC-MS confirm?
Liquid Chromatography–Mass Spectrometry (LC-MS) confirms the peptide's molecular identity by measuring its exact mass-to-charge ratio. This verifies the peptide is what it claims to be — not a related molecule with a similar chromatographic profile.
Why are endotoxin tests run in duplicate?
USP <85> requires duplicate analysis to rule out measurement error. Both replicates must be below the sensitivity threshold (typically ≤0.05 EU/mL) for the batch to pass. Disagreement between replicates triggers a re-test.
Does "Cleared" mean safe for human use?
No. "Cleared" here means the batch meets the USP <85> endotoxin reporting threshold — a standard relevant to laboratory research materials. All products from Oath Research are strictly for research use only and are not approved for human, veterinary, diagnostic, or therapeutic applications.
Are all my orders from this exact batch?
Not necessarily — batches are rotated as inventory moves. Check the batch code on your vial against the test history above to find the matching certificate. Every batch we sell has been independently tested.
Research Use Only
The peptides tested are intended for research use only and are not approved for human or veterinary use, diagnostic, therapeutic, or clinical applications. Results apply only to the specific sample provided and should be interpreted by qualified professionals within the scope of the intended research.