Retatrutide Storage & Stability Datasheet

🖨️ NovaVitality Technical Datasheet
Document ID: NV-DS-RETA-001
Version: 1.1
Effective Date: 10 December 2025
Product: Retatrutide Research Peptide (RUO)


1. Product Overview

ParameterSpecification
INN (Proposed)Retatrutide
CAS StatusProvisional internal code only (INN submitted; CAS pending EMA/FDA assignment)
Molecular FormulaC₁₉₈H₃₀₆N₅₀O₅₈S₁ (sequence-confirmed)
Molecular Weight~4381.0 g/mol (monoisotopic)
SequenceH-Gly-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Lys-Glu-Phe-Ile-Ala-Trp-Leu-Val-Lys-Gly-Arg-Gly-NH₂
Receptor ProfileBalanced triple agonist: GLP-1R / GIPR / GCGR
Form SuppliedLyophilised solid (white to off-white powder)
Purity (HPLC-UV)≥98% (gradient elution, C18 column)
Endotoxin<1.0 EU/mg (LAL kinetic assay)
Residual SolventsMeets ICH Q3C Class 3 limits (≤5000 ppm total)
RUO StatusFor research use only — not for human or veterinary use

2. Recommended Storage Conditions

Unopened (Lyophilised)

ConditionStability DurationNotes
−20°C, desiccated, dark≥24 monthsPreferred long-term storage. Use airtight secondary container with desiccant (e.g., silica gel).
2–8°C (refrigerated)≤6 monthsAcceptable for short-term; monitor for clumping or discolouration.
Room Temp (≤25°C)≤7 daysFor transit only. Avoid humidity (>60% RH accelerates degradation).

📌 Do not store lyophilised peptide in frost-free freezers (temperature cycling causes moisture ingress).

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 for GCGR-domain stability
Bacteriostatic water (0.9% BA)≤48 hours≤3 months (aliquoted)Benzyl alcohol may enhance solubility but monitor for aggregation
Sterile PBS (pH 7.4)≤24 hoursNot recommendedRisk of rapid fibril formation due to neutral pH

⚠️ Critical:
Aliquot before freezing — limit freeze–thaw cycles to ≤3.
Avoid repeated warming/cooling — GCGR-active peptides show accelerated β-sheet aggregation after cycle 2.
– Use low-binding tubes (e.g., LoBind Eppendorf) to minimise adsorption loss.


3. Stability Indicators & Degradation Risks

Risk FactorEffect on RetatrutideDetection Method
Moisture exposureHydrolysis at Asp⁹, Asp¹⁴; succinimide formationHPLC peak broadening, +18 Da MS shift
Oxidation (Met, Trp, Cys¹)Methionine sulfoxide (+16 Da), Trp oxidationLC-MS, loss of receptor potency in cAMP assays
Aggregation/fibrillationVisible haze, precipitate, or gelationDynamic light scattering (DLS), Thioflavin T assay
pH >7.0Rapid deamidation (Asn, Gln), backbone cleavageCE, ion-exchange HPLC
Repeated freeze–thawIrreversible oligomerisationSEC-HPLC, reduced bioactivity in cell assays

🔬 Tip: Run a quick spot-check HPLC before critical assays if material has been stored >3 months.


4. Reconstitution Protocol (Best Practice)

  1. Equilibrate vial to room temp (15–30 min) before opening to prevent condensation.
  2. Centrifuge briefly (5 sec) to collect powder.
  3. Add solvent slowly down vial wall (e.g., 1 mL for 10 mg → 10 mg/mL stock).
  4. Gently swirldo not vortex.
  5. If undissolved: warm to ≤37°C for 2–5 min + low-power sonication (≤30 sec, ice-cooled bath).
  6. Filter through 0.22 µm PVDF (low-protein-binding) for cell work.
  7. Aliquot into pre-chilled tubes. Flash-freeze in liquid N₂ or dry ice/ethanol. Store at −80°C.

5. Analytical Verification (Post-Storage)

TestAcceptance CriteriaWhen to Run
HPLC Purity≥95% main peakAfter >6 months storage, or pre-critical assay
MS IdentityObserved MW ±2 Da of theoreticalAnnually, or after suspected contamination
Endotoxin<5 EU/mL in reconstituted solutionBefore in vivo or primary cell studies
Bioactivity (Optional)EC₅₀ within 2-fold of CoA (cAMP GLP-1R assay)For longitudinal studies or publication prep

6. References & Compliance

  • Jastreboff et al. N Engl J Med 2023; 389:296–307. DOI: 10.1056/NEJMoa2301972
  • ICH Q1A(R2): Stability Testing of New Drug Substances
  • USP <1079>: Good Storage and Distribution Practices
  • EMA Guideline on Peptide Impurities (EMA/CHMP/ICH/107464/2022)
  • MHRA Guidelines on the Labelling of Unlicensed Medicines (2024) — for reference only (RUO not subject, but aligns with handling ethos)

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.