UPB BPC-157 10MG

UPB BPC-157 10mg — Research Peptide with Batch Documentation

UPB BPC-157 10mg is a laboratory research peptide supplied as white lyophilized powder. The accompanying Freedom Diagnostics Certificate of Analysis identifies the submitted samples as BPC-157 and provides analytical findings for lot 11013-004.

The report includes individual purity and net content measurements for three tested vials. Review the complete certificate and match its lot number with the supplied product label before using it as a batch reference.

Purity

The analytical results section reports 99.55% purity by HPLC-UV. The sample summary lists:

• Vial 1: 99.55%
• Vial 2: 99.56%
• Vial 3: 99.55%

Identity testing by LC-MS identifies the material as BPC-157. These findings apply to the submitted samples and do not establish identical results for every vial.

Form

White lyophilized powder. This appearance is documented in the Certificate of Analysis.

Quantity

Labeled quantity: 10 mg.

Reported average net content: 12.15 mg across three tested vials. Individual measurements are:

• Vial 1: 12.27 mg
• Vial 2: 12.22 mg
• Vial 3: 11.97 mg

The labeled quantity and measured sample results are separate figures. The reported average does not guarantee that every vial contains exactly 12.15 mg.

Batch / Lot Number

11013-004. Match this number with the lot printed on the supplied vial before relying on the linked analytical report.

Certificate of Analysis

• Testing laboratory: Freedom Diagnostics
• Client: Ultra Pure Bioscience
• Product: BPC-157 10mg
• Accession / report number: 2605250072
• Search code: Ultr2605250072
• Received date: May 25, 2026
• Reported date: May 25, 2026
• Batch / lot: 11013-004
• Identity: BPC-157, confirmed by LC-MS
• Summary purity result: 99.55% by HPLC-UV
• Average net content: 12.15 mg

View the BPC-157 10mg Certificate of Analysis for the complete laboratory findings.

Additional Analytical Findings

Endotoxin: Both replicates are reported as Pass. The certificate describes a Limulus Amebocyte Lysate assay in accordance with USP <85> and lists assay sensitivity as ≤0.05 EU/mL. This sensitivity figure is not a measured endotoxin concentration.

Microbial analysis: The PCR-based assay reports No Detectable Microbial DNA and a Pass result. This finding relates to the assay’s microbial targets and does not establish sterility.

The linked certificate does not include heavy metal test results.

Handling & Storage

The certificate does not specify storage temperatures, shelf life, or conditions after preparation. Obtain the manufacturer’s product-specific handling and storage instructions before laboratory use.

Record the lot number in laboratory documentation. Analytical results alone do not establish storage stability or an expiration date.

Research Use Only

Supplied as a dry lyophilized powder. Research supplies, including Reconstitution Solution, are sold separately.

This product is not supplied as an FDA-approved medication. It is intended strictly for laboratory, analytical, and scientific research purposes. It is not intended for human or veterinary use, consumption, administration, diagnosis, prevention, or therapeutic application.

Frequently Asked Questions About BPC-157 10mg

What is UPB BPC-157 10mg?

UPB BPC-157 10mg is a laboratory research peptide supplied as white lyophilized powder with a labeled quantity of 10 mg. Its linked certificate documents findings for samples from lot 11013-004.

What purity does the BPC-157 COA report?

The analytical results section reports 99.55% purity by HPLC-UV. Individual measurements across three tested vials range from 99.55% to 99.56%.

Is this product supplied as powder or liquid?

The certificate records the appearance as white lyophilized powder.

Why does the report list 12.15 mg for a 10 mg product?

The product’s labeled quantity is 10 mg. The laboratory reports average net content of 12.15 mg from three submitted vials. These sample-specific measurements do not establish the exact content of every vial.

Does the microbial PCR result confirm sterility?

No. The report records no detectable microbial DNA using the specified PCR-based assay. It does not include a sterility test result.

How can I identify the matching certificate?

Check search code Ultr2605250072, accession number 2605250072, and lot 11013-004. Match the lot with the supplied product label.