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Third-party HPLC + mass spec on every lot
Verified — all release criteria met
released

Certificate of analysis

Ipamorelin

Lot CP-IPAMOR4L-2602C · 10 mg

99.62 %

HPLC purity

Spec ≥ 99.0 %

89.4 %

Net peptide content

By amino acid analysis

< 0.57

Endotoxin (EU/mg)

Spec < 5.0 EU/mg

Provenance

Testing laboratory
Aurum Bioanalytics
Accreditation
ISO/IEC 17025:2017
Country of synthesis
United States
Manufactured
Feb 17, 2026
Release tested
Feb 26, 2026 (7 months ago)
Retest date
Feb 17, 2028
CAS number
170851-70-4
Molecular formula
C38H49N9O5
Theoretical mass
711.86 Da
Observed mass (LC-MS)
712.17 Da (Δ 0.31 Da)

Assay results

Every line the release panel ran for this lot, with the method, the acceptance criterion and the measured value — not a pass mark alone.

Certificate of analysis — assay results
MethodParameterSpecificationResult
RP-HPLC (UV 214 nm)Purity (area %)≥ 99.0 %99.62 %Pass
LC-MS (ESI+)Identity — observed mass711.86 ± 1.0 Da712.17 DaPass
Amino acid analysisNet peptide content≥ 80.0 %89.4 %Pass
Karl FischerWater content≤ 8.0 %4.58 %Pass
Ion chromatographyResidual TFA≤ 1.0 %0.06 %Pass
LAL kinetic chromogenicBacterial endotoxin< 5.0 EU/mg< 0.57 EU/mgPass
USP <71> membrane filtrationSterilityNo growthNo growthPass
Visual / USP <790>AppearanceWhite to off-white cake, free of visible particulatesConformsPass
Chiral RP-HPLC vs. reference standardDiastereomeric purity (D-residue configuration)≥ 99.0 %99.88 %Pass

Sequence

H-Aib-His-D-2-Nal-D-Phe-Lys-NH2

Handling for this lot

Appearance
White lyophilised powder
Storage
-20 °C lyophilised; 2–8 °C reconstituted for up to 30 days
Reconstitution
Dissolves immediately. A vial that resists dissolution is not behaving like ipamorelin.

Other lots of Ipamorelin

Compare batch to batch. Consistency across lots is a stronger signal than any single certificate.

Research use only. This certificate describes material supplied strictly for laboratory research. It is not a drug, food, cosmetic or medical device, has not been evaluated by the FDA, and is not intended for human or veterinary administration of any kind.