For laboratory research use only. Not for human or veterinary use.
PS-RETA-2606
Analysis summary

Retatrutide

Sample as received: Retatrutide

Reference
PS-RETA-2606
SKU
RETA-10MG
Presentation
Lyophilised powder
Analysis date
1 June 2026

Purity

99.20% HPLC-UV + LC-MS (ESI+)

Basis: Peak Purity Index — spectral homogeneity of the main peak.

Identity

Confirmed by mass spectrometry

Expected mass
4731.40 Da
Detected mass
4730.40 Da
Method
HPLC-UV + LC-MS (ESI+)
Detection
UV 215 nm (±4 nm)

Peak integration

#ComponentRT / minArea %TailingPlates NIdentity
1Retatrutide9.84599.201.787,881Confirmed

Area % the peak’s share of total integrated UV area. Tailing peak symmetry. Plates N column efficiency.

Sample as received

Form
Lyophilised powder
Colour
White
Condition
As expected
Peaks resolved
1

Notes

Single chromatographic peak. Purity reported as Peak Purity Index. Identity confirmed by mass spectrometry; MW calculated from m/z 1183.65 [M+4H]⁴⁺.

Testing

Analysed by an independent third-party analytical laboratory in the United Kingdom using established HPLC and LC-MS methods. The laboratory’s identity, the certificate it issued and its supporting records are released to verified research institutions on request.

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