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Research Use OnlyThird-Party Tested in the USABatch-Verified COAsShips from the United StatesPrecision · Purity · PerformanceResearch Use OnlyThird-Party Tested in the USABatch-Verified COAsShips from the United StatesPrecision · Purity · PerformanceResearch Use OnlyThird-Party Tested in the USABatch-Verified COAsShips from the United StatesPrecision · Purity · Performance

Research use only·All materials are supplied to qualified research purchasers for in-vitro laboratory use. Not for human or veterinary use. Research Use Agreement

Analytical Testing

How to read a retatrutide certificate of analysis

A certificate is only useful if it is traceable to the specific vial. This page walks the fields on a real retatrutide certificate and shows what each one does and does not prove.

Last scientific review
September 2026
Published by
Pure Helix

The fields, one at a time

FieldExampleWhat it tells you
Lot numberPH260501The unique batch identifier. It must match the vial label exactly.
Compound and fill weightRetatrutide, 10 mgWhich material and which fill the certificate covers.
Assay date1 June 2026When the measurement was taken. It is a snapshot, not a guarantee going forward.
MethodRP-HPLC, UV 214 nmHow purity was measured. Without this the percentage is not comparable.
Purity result99.9% areaProportion of detected, column-eluting material in the main peak.
Content11.83 mgQuantified peptide per vial from the content assay.
IdentityLC-MS mass confirmationThat the observed mass matches the calculated mass for the sequence.
Verification codeCOA8810Our internal reference tying the published page to the signed source document.

How Pure Helix lot numbers are constructed

Lot identifiers follow the pattern PH + YYMM + sequence. In PH260501, PH is the Pure Helix prefix, 2605 is the year and month the lot entered testing, and 01 is a sequence number within that month — not a calendar day. Each fill weight is a separate lot: the 10, 20 and 30 mg retatrutide vials carry PH260501, PH260502 and PH260503 respectively.

Checking a certificate against a vial

  • Read the lot from the vial label first, then open the matching lot page — do not work the other way round.
  • Confirm the fill weight on the certificate matches the fill weight on the label.
  • Confirm the assay date precedes the date you received the material.
  • Open the signed source document from the lot page rather than relying on a transcribed figure.
  • Record the lot number in your own notes. Any comparative result you generate is only reproducible if the exact material is traceable.

When a lot has no certificate yet

Backordered fill weights show the release flow instead of a certificate: reserved, arriving for testing, sample sent to the laboratory, independent testing, results verified, released to ship. A lot page is published only once a certificate exists for that lot, so an unpublished lot is exactly what it appears to be — untested at this point in the process.

Research use

Pure Helix supplies materials for laboratory research use only. Nothing on this page is medical advice, and none of the material described is for human or veterinary use.

Primary literature and standards

  1. ICH Q2(R2) — Validation of Analytical Procedures
  2. Manning MC et al. Stability of protein pharmaceuticals: an update. Pharm Res. 2010.

Reference materials and documentation

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