Batch report — full panel

RET-20-V-2604-001

Retatrutide vial line (10mg and 40mg formats) — the only batch in this catalog with the full sterility-grade panel: 99.741% HPLC, 20.92 mg assay, heavy metals not detected, TFA not detected, bacterial endotoxin 1.449 EU/Vial. Each report has its own Janoshik verification key.

For in-vitro laboratory research only. Not for human or veterinary use.

Batch facts

Products
Retatrutide 10mg Vial · Retatrutide 40mg Vial
Batch number
RET-20-V-2604-001
Molecule
Retatrutide (LY-3437943) — CAS 2381089-83-2
Purity (HPLC)
99.741%
Assay
20.92 mg retatrutide
Heavy metals
As, Cd, Pb, Hg — not detected
TFA
Not detected
Endotoxin (LAL)
1.449 EU/Vial
Laboratory
Janoshik Analytical
Analysis dates
21–24 April 2026
Verification keys
Purity YCYA75M373NA · Heavy metals GHHWTCPUSEZ7 · TFA NUA8B6XPAMWZ · Endotoxin E8ZFE17MI47D

Purity & assay report

HPLC purity at 99.741% with 20.92 mg quantitative assay.

Janoshik purity and assay report for batch RET-20-V-2604-001 — 99.741% HPLC, 20.92 mg assay

Heavy metals report

ICP-MS panel for arsenic, cadmium, lead and mercury. All four below detection limits.

Janoshik heavy metals report for batch RET-20-V-2604-001 — As, Cd, Pb, Hg not detected

TFA report

Trifluoroacetic acid is a residual solvent from peptide synthesis. HPLC purity does not see it. This batch tests separately and returns "not detected."

Janoshik TFA report for batch RET-20-V-2604-001 — TFA not detected

Bacterial endotoxin (LAL) report

Limulus Amebocyte Lysate assay returns 1.449 EU/Vial. Endotoxin is the sterility benchmark pharma uses for release testing.

Janoshik endotoxin report for batch RET-20-V-2604-001 — 1.449 EU/Vial

Common questions

What is batch RET-20-V-2604-001?
Retatrutide vial line covering both 10mg and 40mg formats. Janoshik ran a full panel 21–24 April 2026: 99.741% HPLC, 20.92 mg retatrutide assay, heavy metals (As, Cd, Pb, Hg) not detected, TFA not detected, bacterial endotoxin 1.449 EU per vial.
What does 1.449 EU per vial mean?
EU is endotoxin units, measured via the LAL (Limulus Amebocyte Lysate) assay. 1.449 EU per vial is the bacterial endotoxin load found in the vial. Endotoxin is the sterility benchmark pharma uses for release testing. Most research peptide sellers skip it; this batch publishes the number.
Why test for TFA separately?
TFA (trifluoroacetic acid) is a common residual solvent from peptide synthesis. HPLC purity does not see it. Testing separately confirms it is not present. For this batch, TFA was not detected.
How do I verify each Janoshik report?
Go to janoshik.com and paste the relevant verification key. Purity: YCYA75M373NA. Heavy metals: GHHWTCPUSEZ7. TFA: NUA8B6XPAMWZ. Endotoxin: E8ZFE17MI47D. Each returns the original report off Janoshik's server.

Source these vials from Remy Peptides

Both the 10mg and 40mg vial SKUs ship under batch RET-20-V-2604-001 while it remains the current vial batch.