CJC-1295 No DAC Storage & Stability Datasheet

🖨️ NovaVitality Technical Datasheet
Document ID: NV-DS-CJCND-001
Version: 1.0
Effective Date: 10 December 2025
Product: CJC-1295 No DAC (Modified GRF 1–29) Research Peptide (RUO)


1. Product Overview

ParameterSpecification
INN (Proposed)CJC-1295 No DAC (Modified GRF 1–29)
CAS Status876168-09-9 (assigned)
Molecular FormulaC₁₅₂H₂₅₄N₄₄O₄₂
Molecular Weight3367.95 g/mol (monoisotopic, C-terminal amidated)
SequenceH-Tyr-DAla-Asp-Ala-Ile-Phe-Thr-Gln-Ser-Tyr-Arg-Lys-Val-Leu-Ala-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Leu-Ala-Arg-NH₂
(Key stabilising mods: DAla², Glu⁸, Leu¹⁵, Ala²⁷)
Receptor ProfileSelective agonist: GHRHR (EC₅₀ ≈ 1.8 nM); no GHRP or ghrelin receptor activity
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. D-Ala² and amidation confer high stability. 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.

📌 CJC-1295 No DAC is stable lyophilised, but Phe⁶ and Leu residues are hydrophobic — moisture promotes aggregation. NovaVitality uses argon headspace in all vials.

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 core
Bacteriostatic water (0.9% BA)≤48 hours≤3 months (aliquoted)Acceptable; benzyl alcohol aids solubilisation
PBS (pH 7.4)≤24 hoursNot recommendedHigh risk of aggregation (hydrophobic collapse)

⚠️ Critical:
Aliquot before freezing — limit freeze–thaw to ≤3 cycles (hydrophobic peptides aggregate irreversibly after cycle 3).
– Use low-binding tubes (e.g., LoBind Eppendorf) — hydrophobic adsorption is significant.
– Avoid repeated warming — promotes surface adhesion.


3. Stability Indicators & Degradation Risks

Risk FactorEffect on CJC-1295 No DACDetection Method
Moisture exposureHydrolysis at Asp³, Gln⁸HPLC peak broadening, +18 Da MS shift
Oxidation (Met⁰ absent; Phe⁶ present)Phe oxidation (rare)LC-MS: +16 Da; ↓ receptor potency
AggregationVisible haze, precipitateDLS (>300 nm), SEC-HPLC high-MW peak
DPP-4 exposureCleavage at Tyr¹–DAla² (resistant, but not absolute)LC-MS: −250 Da (Tyr-DAla); ↓ cAMP response
Repeated freeze–thawIrreversible oligomerisationLoss of GHRHR potency (EC₅₀ shift >2-fold)

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


4. Reconstitution Protocol (Best Practice)

  1. Equilibrate vial to room temp (15–30 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 LoBind tubes, flash-freeze in liquid N₂, 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
LC-MS IdentityObserved MW 3368.0 ±2.0 DaAnnually, or after suspected contamination
Endotoxin<5 EU/mL in reconstituted solutionBefore in vivo or primary cell studies
Bioactivity (Required)EC₅₀ ≤ 2.5 nM at hGHRHR (cAMP, HEK293)For all publication or longitudinal studies

6. References & Compliance

  • Veldhuis JD et al. J Clin Endocrinol Metab. 2007;92(3):957–964. DOI: 10.1210/jc.2006-2115
  • Alba M et al. Growth Horm IGF Res. 2017;35:1–8. DOI: 10.1016/j.ghir.2017.05.003
  • ICH Q1A(R2): Stability Testing of New Drug Substances
  • USP <1079>: Good Storage and Distribution Practices
  • 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.