Regenerative research peptides · Reference
BPC-157
Synthetic pentadecapeptide · Also known as Body Protection Compound 157, PL 14736, Pentadecapeptide BPC 157
BPC-157 is a 15-residue synthetic peptide studied in rodent models of tissue repair. The sequence is short but contains a Pro-Pro-Pro tract that is notoriously difficult to couple cleanly during solid-phase synthesis — making independent purity verification the difference between knowing what is in the vial and guessing.
Chemistry at a glance
- CAS
- 137525-51-0
- Formula
C62H98N16O22- Avg. MW
- 1419.55 Da
- Monoisotopic
- 1418.7128 Da
- Sequence
GEPPPGKPADDAGLV
Chemistry summary only. CertikLabs does not publish dosing, administration, or clinical guidance for any peptide.
Structure and chemistry
BPC-157 is a linear pentadecapeptide with the one-letter sequence GEPPPGKPADDAGLV. The molecular formula is C62H98N16O22 with an average molecular weight near 1419.5 Da and a theoretical monoisotopic mass of 1418.7128 Da. CAS registry: 137525-51-0.
The sequence is derived from a 62 kDa human gastric juice protein called Body Protection Compound (BPC); residues 1–15 of the parent define BPC-157. There is no native post-translational modification on this fragment, so all material in circulation is fully synthetic.
Synthesis and where impurities come from
BPC-157 is produced by standard Fmoc solid-phase peptide synthesis (SPPS). Two regions of the sequence are responsible for most of the impurity burden:
- The Pro-Pro-Pro tract at positions 3–5. Proline is a difficult coupling partner because of steric hindrance at the secondary amine; three in a row is a well-documented source of deletion sequences and incomplete coupling.
- The Asp-Asp segment at positions 10–11. Aspartate is prone to aspartimide formation under repeated piperidine deprotection, which can rearrange to α- and β-aspartyl products and racemized D-Asp.
A complete impurity profile from a real batch typically includes deletion sequences, C-terminal truncations, D-Pro racemers, aspartimide-derived isomers, oxidation products from storage, and residual TFA counter-ion from cleavage. See common peptide impurities for the full taxonomy.
How CertikLabs verifies BPC-157
The standard CertikLabs panel for a BPC-157 batch:
- RP-HPLC purity (C18, 0.1% TFA / MeCN, UV 214 nm)
- LC-MS identity (ESI-Q-TOF, observed vs theoretical monoisotopic mass)
- Quantitative AAA for content
- Ion chromatography for TFA / acetate counter-ion
- Karl Fischer for water content
Each method, including column, mobile phase, gradient, and detection conditions, is reported on the Certificate of Analysis so the result is reproducible. See how to read a peptide COA for what each section should contain.
Published mechanism (literature summary)
Published rodent literature describes activity on angiogenesis (VEGFR2 pathway), nitric oxide signaling, and growth-factor expression in injured tissue. No clinical efficacy or safety claims are made here.
Primary sources:
- Sikiric P. et al., Stable gastric pentadecapeptide BPC 157 — review.(PMID 29879886)
- Chang C.H. et al., BPC 157 promotes tendon outgrowth in vitro.(PMID 21030672)
CertikLabs does not publish dosing, administration routes, or clinical recommendations for BPC-157.
Stability and storage (chemistry only)
Lyophilized BPC-157 is generally stable at -20°C protected from light and moisture. Reconstituted in bacteriostatic or sterile water, stability is shorter and degradants (oxidation, deamidation, aggregation) accumulate; analytical re-test of any working solution is the only reliable confirmation.
Frequently asked questions
What is BPC-157?
BPC-157 is a synthetic 15-residue peptide (sequence GEPPPGKPADDAGLV) derived from a fragment of human gastric juice protein BPC. CAS 137525-51-0, molecular formula C62H98N16O22, average mass approximately 1419.5 Da. It is a research compound; CertikLabs verifies the chemistry of supplied material and does not publish dosing or clinical guidance.
How is BPC-157 purity tested?
Purity is measured by reverse-phase HPLC on a C18 column with a 0.1% TFA / acetonitrile gradient and UV detection at 214 nm, with the full method (column, mobile phase, gradient, detection wavelength) reported on the Certificate of Analysis. Identity is confirmed by LC-MS against the theoretical monoisotopic mass of 1418.71 Da.
What are the most common BPC-157 impurities?
Deletion sequences across the Pro-Pro-Pro tract (a known difficult-coupling region), C-terminal truncations, D-Pro racemization, aspartimide formation at the Asp-Asp segment, and residual TFA counter-ion from cleavage. These are the analytes a well-designed RP-HPLC method is expected to resolve from the main peak.
How can I verify a BPC-157 Certificate of Analysis?
An independent CertikLabs Certificate of Analysis is content-hashed (SHA-256) and anchored on a public blockchain at issuance. Anyone holding the report can recompute the hash and confirm it matches the on-chain record — the document is tamper-evident without trusting any single party.
Published 2026-05-16