Retatrutide research material and lot reports

Review available documentation by material, nominal quantity and lot. Choose a listing:

Ships from the U.S. with trackingFree U.S. shipping at $99Match material, quantity and lotLaboratory research use only · 21+
Research-use scope. Laboratory, analytical, educational, and in-vitro research only. Not for use in people or animals. This page describes identity and documentation; it contains no handling or procedural guidance.

Identity

FieldValue
MaterialRetatrutide
CAS number2381089-83-2
Molecular formula—
Molecular weight—
FormLyophilized powder in a sealed vial

Retatrutide 10 mg is a synthetic peptide (CAS 2381089-83-2) supplied as a lyophilized powder in a sealed 10 mg vial, the smallest of four Retatrutide vial sizes.

Listings by strength

StrengthPriceBatch documentationListing
10mg$69.99Lot RT-2502-A — 99.83% (HPLC), tested Aug 10, 2026 — batch reportRetatrutide 10mg
20mg$119.99Lot RT-2502-B — 99.90% (HPLC), tested Aug 27, 2026 — batch reportRetatrutide 20mg
30mg$164.99See listing for current statusRetatrutide 30mg
60mg$249.99See listing for current statusRetatrutide 60mg

Published batch documentation

About this material

Retatrutide is the material name used on these listings. The pictured vial labels also use a shorthand name. This shorthand is not a substitute for the full material identity, nominal quantity and lot number when reviewing documentation.

The reports linked above describe the samples and analytical results identified in those reports. Their publication does not establish that every vial currently in stock belongs to the tested lot.

Choosing a nominal quantity

The 10 mg, 20 mg, 30 mg and 60 mg listings state nominal quantities, not different purity grades. A report for one quantity or lot must not be treated as evidence for another. Check the individual listing for documentation availability and contact support if the matching record is missing.

How to compare a vial with a report

  1. Read the material name, nominal quantity and lot number on the vial label.
  2. Compare those details with the sample identification in the report. If they do not match or the connection is unclear, request clarification before relying on the report.
  3. Review the test methods, results and limitations actually stated by the laboratory. A purity percentage alone does not establish identity, quantity or sterility.
  4. Use the issuing laboratory's verification service or contact the laboratory to confirm the report. A link alone does not establish authenticity.

Related reading

Common questions

What does the shorthand on the pictured label mean?
It is label shorthand for Retatrutide. Compare the full material identity, nominal quantity and lot with the applicable report; the shorthand alone does not verify the contents.
Are the four nominal quantities different purity grades?
The quantities listed are not purity grades. Evaluate only the analytical results documented for the matching sample and lot.
Does one report cover all four quantities?
No such coverage should be assumed. A report describes its identified sample and lot. A report for one quantity or lot does not automatically apply to another.
How do I confirm a report is genuine?
Use the issuing laboratory's verification service or contact the laboratory directly with the report identifier. An available PDF or verification link alone does not prove authenticity or connect current stock to the tested sample.

What a batch report does and does not establish

A published report describes one sample from one lot on one date under the stated method. It supports the identity and chromatographic purity result it lists. It does not describe other lots, and it says nothing about attributes that were not tested. Match the lot on the vial label to the lot on the report before relying on it (how to match a vial to its record).

Related documentation