Source format
Raw peptide powder, lyophilized powder, neutral vial format, or optional packaging service depending on the buyer RFQ.
Pepti · BPC-157 + TB-500 blend COA documentation
BPC-157 + TB-500 blend COA documentation
COA documentation guide for BB10-style BPC-157 + TB-500 lyophilized blend inquiries. Pepti confirms exact formula, HPLC purity, MS identity and lot documents before quotation.
Blend inquiry guide
This page is for buyers who ask for BB10-style BPC-157 + TB-500 blend documents. BB10 is handled as inquiry shorthand, listed through Pepti's BB10 / BPC-157 + TB-500 blend quote path. Exact formula and lot-document scope are confirmed before quote.
Product images are finished-vial display examples. Pepti primarily supplies peptide raw powder / lyophilized powder; neutral labels are default, and custom labels or branded packaging are optional services on request.
Raw peptide powder, lyophilized powder, neutral vial format, or optional packaging service depending on the buyer RFQ.
Every production lot includes a batch-linked COA, HPLC chromatogram and MS identity record. Water content, lot code and shipment documents are confirmed by RFQ and production lot.
Send compound list, quantity, target purity, destination market and document needs for a clearer manufacturer quote.
B2B and research procurement only. Buyers confirm local regulatory compliance.
Why two-component COA review is different
For a single peptide, COA review often centers on one HPLC purity value, one MS identity result and one batch number. A co-lyophilized BPC-157 + TB-500 preparation requires documentation that accounts for both compounds independently inside the same finished lot. A COA that reports only “Purity: 98%” without identifying BPC-157 and TB-500 separately is incomplete for two-component review.
CAS 137525-51-0, commonly referenced as a 15-amino-acid peptide in published preclinical literature. The component should be traceable in the analytical record.
CAS 885340-08-9, commonly discussed as a Thymosin Beta-4/TB-500 peptide family reference. The component should not be hidden inside a combined result.
The finished blend should carry one lot reference that connects formula, lyophilization, vial labeling and document pack.
Buyer checklist
| COA | Certificate of Analysis with batch identity, purity result and lot reference. |
|---|---|
| HPLC | Purity chromatogram and peak profile discussion before order confirmation, ideally with component-level review rather than a single combined purity percentage. |
| MS | Mass spectrometry identity confirmation for the stated components. |
| Buyer use | Document review for qualified B2B and research procurement only. |
Five core elements
Ask whether BPC-157 and TB-500 are reviewed separately. Resolved peak evidence is stronger than one combined number that cannot be assigned to either component.
MS identity records should support both stated components. Data for only one compound does not verify the blend as a whole.
BB10-style supply is usually a 1:1 concept, for example 5 mg + 5 mg per vial. The RFQ should state whether 5+5, 10+10 or 15+15 is requested.
Residual moisture is a stability-related parameter for lyophilized peptide preparations. Pepti confirms water content availability by current stock or production RFQ.
The vial label, COA, chromatogram and MS record should connect back to the same production lot, not to unrelated old files.
Independent third-party testing can be arranged when a buyer needs extra verification before scale-up. Pepti does not claim every historical lot followed that path.
Red flags
A one-line purity value does not show whether BPC-157 and TB-500 were each reviewed.
Identity data for one component leaves the second component unconfirmed.
The document should state the requested blend format, such as 5 mg + 5 mg, 10 mg + 10 mg or 15 mg + 15 mg.
Separate old COAs do not prove the current co-lyophilized finished lot.
Missing water-content discussion removes one useful lyophilized-powder quality indicator.
If the COA, vial code and chromatogram cannot be linked, traceability is weak.
Questions before ordering
Pre-purchase documents
For active stock or production RFQs, buyers can request the available COA preview and confirm whether the lot file includes batch-linked COA, HPLC chromatogram, MS identity record, water-content field, neutral label or custom label details and shipment-document requirements.
Eligible sample path starts from 1 kit (10 vials). Production quote depends on RFQ quantity, formula, packaging scope, current stock or production schedule and destination market.
References and standards context
Buyer teams often compare supplier documents against internal QC requirements, pharmacopeial thinking and general analytical principles such as defined specifications, validated identity methods, chromatographic purity review and batch traceability. For co-lyophilized research blends, the practical rule is simple: confirm both components, confirm the lot link and confirm what documents are available before payment.
Related pages
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