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Alluvi Retatrutide 40mg Long-Term Stability Test

Room temperature • Purity • Concentration • pH • Independent Janoshik analysis

Alluvi • Independent analytical information

What makes the Alluvi formulation different?

Alluvi describes its solution process as being designed to keep its research APIs within a controlled formulation environment from filling through storage. The Retatrutide 40mg pen studied here was independently analysed by Janoshik for concentration, purity and pH.

Alluvi subjected the prepared pen to a reported extended room-temperature study and compared analytical results across the study timeline.

Initial checkpoint
56reported days at room temperature
Later checkpoint

Results at a glance

Initial concentration
16.00–16.01 mg/mL
Two Janoshik measurements
Later concentration
15.99 mg/mL
Later degradation-test result
Later purity
98.322%
Independent laboratory result
Later pH
7.66
Independent pH measurement

Study timeline

Stage 1

Initial analytical checkpoint

A Retatrutide 40mg Alluvi pen with a stated 2.4mL fill was assessed during the first stage of the study.

  • Concentration: 16.00 mg/mL and 16.01 mg/mL
  • Purity: 99.651% and 99.592%
  • Calculated content: 38.40mg at 16.00 mg/mL × 2.4mL
  • Janoshik Task: #147173
  • Analysis date: 20 April 2026
Stage 2

Later analytical checkpoint

The later samples were held in Janoshik custody at room temperature before analysis on 19 May 2026.

  • Concentration: 15.99 mg/mL
  • Purity: 98.322%
  • Calculated content: approximately 38.38mg at 15.99 mg/mL × 2.4mL
  • pH: 7.66
  • Documented Janoshik room-temperature custody: 33 days
  • Janoshik Tasks: #165632 and #165637
Key observation: based on the laboratory-reported concentrations and the stated 2.4mL fill volume, calculated content changes from approximately 38.40mg to 38.38mg, a difference of about 0.02mg or 0.06%. Purity changes from 99.651% to 98.322%, a difference of 1.329 percentage points.

Side-by-side analytical results

MeasurementInitial checkpointLater checkpoint
Retatrutide concentration16.00 / 16.01 mg/mL15.99 mg/mL
Calculated content at 2.4mL38.40mg*≈38.38mg*
Purity99.651% / 99.592%98.322%
pHNot shown on initial report7.66

*Calculated from the Janoshik-reported concentration using the stated 2.4mL fill volume. The calculated total content is not a separate laboratory measurement.

Independent Janoshik reports

The original report images are reproduced below so the analytical results, task numbers, batch information and laboratory comments can be reviewed directly. Select an image to open the full-size report.

Janoshik initial Alluvi Retatrutide concentration and purity reportInitial concentration & purityTask #147173 • Batch AR1739JAT
Janoshik Alluvi Retatrutide degradation test reportLater concentration & purityTask #165632 • Batch AR1739JAT
Janoshik Alluvi Retatrutide pH reportLater pH measurementTask #165637 • Batch AR1739JAT

Understanding the 56-day timeline

The 56-day room-temperature period is the overall study timeline stated by Alluvi. The later Janoshik reports specifically record that the samples were received on 16 April 2026 and held in Janoshik custody at room temperature until testing on 19 May 2026, giving a documented laboratory custody period of 33 days.

Keeping these two points separate allows the overall study timeline to be presented while accurately reflecting what the independent laboratory reports themselves document.

View Retatrutide ProductAll Lab ReportsHow to Read a COAResearch Centre

Research-use disclaimer

This page presents analytical information for laboratory research and development context only. It does not provide medical advice, treatment guidance, dosing information, administration instructions or reconstitution instructions.

The analytical results shown do not establish clinical safety, sterility, efficacy, suitability for injection or an authorised shelf life. Products referenced on this website are intended for research and development purposes only and are not intended for human or veterinary use.