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BPC-157 5mg + TB-500 5mg

VP-P4HW9L-5C6Y

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Blend summary %

99.67%

LC-MS (ppm)

17.8

Batch / reference

APOL-LAB-2026-5002

Registry ID

VPK-APOL-2026-5002

Analytical summary

Values as recorded for this batch reference.

Blend summary purity	99.67%
Molecular weight	— Multi-component reference line; MW quoted per analyte where applicable.
HPLC / LC-MS notes	Multi-component chromatogram; resolved regions integrated per validated blend method.
LC-MS (ppm)	17.8
Batch / reference	APOL-LAB-2026-5002
Registry ID	VPK-APOL-2026-5002
Instrument	Agilent 1260 Infinity II
Column	ZORBAX SB-C18, 4.6×150 mm, 3.5 µm
Method	Water / acetonitrile + 0.1% TFA, gradient
Detection	UV 214 nm
Testing date	18 Feb 2026
Notes	Research reference material — chain-of-custody retained per lab SOP. Blend line; stated masses are catalogue descriptors only.
Issued	4 Jun 2026, 13:57

Representative chromatogram

UV trace (normalised). Blend line—composite profile reflects recorded purity class.

Recorded components

Analytes named for this reference line (laboratory traceability).

BPC-157
TB-500 fragment

Component purity

Individual analyte purity values recorded for this blend line.

Analyte	Purity %	RT (min)
BPC-157	99.62	4.23
TB-500 fragment	99.73	4.08

Batch imaging (placeholder)

Batch photograph slot—upload via registry when available.

Additional tests

Requested or recorded supplementary analyses

LC-MS identity (representative)
System suitability

Listed tests reflect requested or recorded scope; execution may be in-house or via partner laboratories depending on method allocation.

Peak table

Integrated peak summary; reported areas sum to the total integration window.

Peak	RT (min)	Area %
TB-500 fragment	4.08	49.83
BPC-157	4.23	49.84
Total (integrated area %)		99.67

Registry data reflects the record as entered or returned for the stated method and scope. Analytical fields may be manually recorded at issuance. Chromatogram traces are representative of the recorded purity class and may be normalised for display.

Partner laboratory note: Depending on method, sample type, and capacity, selected tests—including certain HPLC purity work—may be performed by qualified EU partner laboratories. Method and facility details are stated on the certificate where applicable.

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