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INSTITUTIONAL SUPPLIER

Biosynth

Source-led supplier profile · Reviewed 10 September 2026

Manufacturer / brand review

Biosynth publishes an identifiable research-peptide COA with an unusually important purity-definition caveat: two chemical forms count together.

Inspected sample results

PP51304, H-QPTESIVRF-OH, lot LB22-B1121, issued 20 August 2025: UPLC purity 95.8% (minimum 95%); ESI-MS 1076.6. The TFA-salt certificate states that target peptide and pGlu-form peptide are present in an unknown ratio and both peaks count toward final purity. No measured peptide content is supplied.

Testing methods and purification

The inspected research-grade COA uses UPLC at 215 nm and ESI-MS. GMP service pages separately describe content, solvents, counterions, water, endotoxin and microbial testing.

How often is testing performed?

A dated lot certificate was inspected. GMP release capabilities do not establish a universal test cadence across research catalogue products.

What remains unverified

The COA explicitly counts target and pGlu-form peaks toward purity in an unknown ratio. It does not demonstrate 95.8% of a single form or a clean contaminant panel.

Catalogue snapshot

Custom peptidesResearch reagents

Examples from the linked source, not a complete or real-time stock list. Institutional entries describe service categories. Shipping to Cyprus is not verified.

Why this score?

Points reward evidence maturity, not measured product purity. Claim-only points are limited; unknown criteria remain zero. Full rules are available in Research guidesBusiness decision guidesour methodology.

Purity & identityA sample result with purity/identity data was inspected.10/20
Independent laboratoryNo inspected external-laboratory report earns credit; in-house QC is not independent testing.0/20
Contaminant controlsNo qualifying, product-specific contaminant result inspected. Optional capabilities do not earn result points.0/30
Quantity & traceability5/20: identifiable lot with a dated document (5); no measured peptide-content result earns quantity credit (0). A print or expiry date does not establish analysis timing.5/20
AccountabilityPublic business/contact and product-use context; no independent audit of the operator.5/10

Verification limits

Lab attribution: Biosynth in-house certificate. A laboratory-hosted record, where explicitly identified, was inspected on the lab’s portal. No direct staff confirmation, blind purchase, independent sampling or full current-batch audit was performed by Peptide.cy. Absence of a recorded test is not proof of contamination.

Public claims about purification cost, manufacturing location or certifications are not treated as proof of a clean final product. An authenticated COA would still apply only to its identified sample.

Follow the evidence

Sources accessed 10 September 2026. Vendor claims and vendor-hosted reports are identified as such.

  1. Biosynth — official source ↗
  2. Testing document — PP51304 Lot LB22 B1121 20250820.pdf ↗
  3. Testing document — gmp peptides ↗
COMMUNITY, WITH CONTEXT

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