Ipamorelin Storage & Stability Datasheet

🖨️ NovaVitality Technical Datasheet
Document ID: NV-DS-IPAM-001
Version: 1.0
Effective Date: 10 December 2025
Product: Ipamorelin Research Peptide (RUO)


1. Product Overview

ParameterSpecification
INN (Proposed)Ipamorelin
CAS Status170903-93-8 (assigned)
Molecular FormulaC₃₈H₄₉N₉O₅
Molecular Weight711.86 g/mol (monoisotopic, C-terminal amidated)
SequenceH-Aib-His-D-2-Nal-D-Phe-Lys-NH₂
(Aib = α-aminoisobutyric acid; D-2-Nal = D-2-naphthylalanine)
Receptor ProfileSelective agonist: GHSR-1a (EC₅₀ ≈ 4.2 nM); no significant activity at CRF, prolactin, or GHRH receptors
Form SuppliedLyophilised Solid (white to off-white powder)
Purity (HPLC-UV)≥98% (gradient elution, C18, 220 nm)
Endotoxin<1.0 EU/mg (LAL kinetic assay)
Residual SolventsMeets ICH Q3C Class 3 limits
RUO StatusFor research use only — not for human, veterinary, diagnostic, or therapeutic use

2. Recommended Storage Conditions

Unopened (Lyophilised)

ConditionStability DurationNotes
−20°C, desiccated, dark≥24 monthsPreferred. Aib and D-amino acids confer high protease resistance. Use airtight secondary container.
2–8°C (refrigerated)≤6 monthsAcceptable for active lab use; monitor for cake integrity.
Room Temp (≤25°C)≤7 daysFor transit only. Avoid humidity >60% RH.

📌 Ipamorelin is highly stable lyophilised due to non-natural residues (Aib, D-2-Nal, D-Phe), but aromatic side chains (D-2-Nal, D-Phe) are light-sensitive — amber vials with argon headspace are used.

Reconstituted (Solution)

SolventShort-Term (2–8°C)Long-Term (−80°C)Notes
0.1% acetic acid in 0.9% NaCl≤72 hours≤6 months (aliquoted)Preferred — enhances solubility of hydrophobic D-2-Nal/D-Phe
Bacteriostatic water (0.9% BA)≤48 hours≤3 months (aliquoted)Acceptable; benzyl alcohol aids solubilisation
PBS (pH 7.4)≤24 hoursNot recommendedRisk of precipitation (hydrophobic collapse)

⚠️ Critical:
Aliquot before freezing — limit freeze–thaw to ≤3 cycles (aromatic peptides aggregate irreversibly after cycle 3).
– Use low-binding tubes (e.g., LoBind Eppendorf) — hydrophobic adsorption is significant.
– Store solutions in amber tubes or wrap in foil — D-2-Nal is photosensitive.


3. Stability Indicators & Degradation Risks

Risk FactorEffect on IpamorelinDetection Method
Light exposure (UV/vis)D-2-Nal oxidation → quinone derivatives (+16/+32 Da)LC-MS: +16/+32 Da peaks; ↓ GHSR-1a potency
Oxidation (His²)2-oxo-histidine (+16 Da)LC-MS/MS; reduced receptor binding
Acid hydrolysis (Lys⁵)Deamidation → allysineRare — monitor HPLC peak tailing
AggregationVisible haze, precipitateDLS (>200 nm), SEC-HPLC high-MW peak
Repeated freeze–thawIrreversible dimerisation (>3 cycles)Loss of cAMP response (EC₅₀ shift >2-fold)

🔬 Tip: Run a quick cAMP assay (HEK293-GHSR-1a) before critical in vivo studies — functional validation is more sensitive than purity alone.


4. Reconstitution Protocol (Best Practice)

  1. Equilibrate vial to room temp (15 min) in dark (protect D-2-Nal).
  2. Centrifuge briefly (5 sec) to collect powder.
  3. Add 0.1% acetic acid/saline slowly down vial wall (e.g., 1 mL for 10 mg → 10 mg/mL).
  4. Gently swirldo not vortex.
  5. If undissolved: warm to ≤37°C for 2 min + low-power sonication (≤30 sec, ice-cooled bath, in dark).
  6. Filter through 0.22 µm PVDF (low-protein-binding, amber-filtered if possible).
  7. Aliquot into pre-chilled LoBind amber tubes, flash-freeze in liquid N₂, store at −80°C (dark).

5. Analytical Verification (Post-Storage)

TestAcceptance CriteriaWhen to Run
HPLC Purity≥95% main peakAfter >6 months storage, or pre-critical assay
LC-MS IdentityObserved MW 711.9 ±1.0 DaAnnually, or after suspected oxidation
Endotoxin<5 EU/mL in solutionBefore in vivo or primary cell studies
Bioactivity (Required)EC₅₀ ≤ 5.0 nM at hGHSR-1a (cAMP, HEK293)For all publication or longitudinal studies

6. References & Compliance


7. Support & Documentation

📧 Technical queries: [email protected]

🔒 This datasheet is for informational purposes only. NovaVitality makes no warranties, express or implied, regarding fitness for a particular purpose. Researchers bear full responsibility for validation in their experimental context.