For Research Use OnlyNot for Human Consumption

Our most-documented batch. Janoshik ran a full panel from 21 to 24 April 2026: 99.741% HPLC, 20.92 mg retatrutide assay, heavy metals (As, Cd, Pb, Hg) not detected, TFA not detected, and bacterial endotoxin 1.449 EU/Vial via LAL. Endotoxin is the sterility benchmark pharma uses for release testing. Most research peptide sellers skip it. We publish it.

Product
ProPeptide Retatrutide vial line (10mg and 40mg formats)
Batch number
RET-20-V-2604-001
Molecule
Retatrutide (LY3437943), CAS 2381089-83-2
Purity (HPLC)
99.741%
Assay
20.92 mg retatrutide
Heavy metals (As, Cd, Pb, Hg)
Not detected
Residual TFA
Not detected
Bacterial endotoxin (LAL)
1.449 EU/Vial
Laboratory
Janoshik Analytical
Sample received
15 April 2026
Analysis dates
21–24 April 2026
Purity verify key
YCYA75M373NA
Heavy metals verify key
GHHWTCPUSEZ7
TFA verify key
NUA8B6XPAMWZ
Endotoxin verify key
E8ZFE17MI47D
Janoshik purity and assay report for batch RET-20-V-2604-001
Purity + Assay
Common GLP-1 peptide blind test
99.741% HPLC · 20.92 mg assay
Verify key YCYA75M373NA
Janoshik heavy metals report for batch RET-20-V-2604-001
Heavy metals
As, Cd, Pb, Hg analysis
All four not detected
Verify key GHHWTCPUSEZ7
Janoshik TFA report for batch RET-20-V-2604-001
Residual solvent
TFA analysis
Not detected
Verify key NUA8B6XPAMWZ
Janoshik endotoxin report for batch RET-20-V-2604-001
Sterility benchmark
Bacterial endotoxin (LAL)
1.449 EU/Vial
Verify key E8ZFE17MI47D
What is batch RET-20-V-2604-001?
ProPeptide 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/Vial.
What does 1.449 EU/Vial mean?
EU is endotoxin units, measured via the LAL (Limulus Amebocyte Lysate) assay. 1.449 EU/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?
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.
What product ships with batch RET-20-V-2604-001?
The ProPeptide Retatrutide 10mg vial and 40mg vial ship under the same vial-line batch.