Analytical Release Document · Retatrutide 40 mg

Certificate of Purity

Every batch released by Matrix Lab inc. is accompanied by a signed Certificate of Purity — the documented evidence that identity, potency and freedom from contamination were confirmed before dispatch.

Specimen · Certificate of Purity Matrix Lab inc. Certificate of Analysis — Retatrutide 40 mg, lot RT0612DE

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What it certifies

Proof of purity, attached to the lot.

Analytical results for Retatrutide 40 mg, lot RT0612DE, quantified by UHPLC-UV-PDA. The certificate ties strength, purity and impurity profile to a single, verifiable batch identity that follows the product to the point of care.

LotRT0612DE
Strength (spec. 40 mg)41.59 mg
Purity (spec. ≥98%)99.29%
Single impurity (spec. ≤1%)0.44%
Total impurities (spec. ≤2%)0.27%
Appearance (white powder)PASS
pH (spec. 6.0 – 8.0)6.2
MethodUHPLC-UV-PDA-QDA

Demonstration document. The values shown are representative of a released lot. The purity data printed on your physical certificate reflects the actual analytical results for the specific lot in your possession. Confirm any lot against our release register on the batch verification page.

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Quantitative potency

HPLC assay confirms the active is present at label claim — no under- or over-dosing hidden behind a formulation.

Freedom from contamination

Sterility and endotoxin testing screen every sterile lot before a single unit is authorized for release.

Signed & traceable

Each certificate carries a serialized lot identity, so the purity record can be reconciled to the product in hand.