This website is currently under construction but will be available shortly. Check back soon!

Ipamorelin + CJC-1295 (No DAC) — Synergistic Growth Hormone Secretagogue Research Peptide Combination | Klene Peptides

For Research Use Only | Not for Human or Veterinary Administration

Ipamorelin and CJC-1295 without DAC represent two mechanistically distinct growth hormone (GH) secretagogues that, when combined in research protocols, produce synergistic amplification of pulsatile GH release through simultaneous engagement of separate receptor pathways. Ipamorelin acts as a selective agonist at the ghrelin/GH secretagogue receptor (GHSR-1a), while CJC-1295 without DAC — also known as Modified GRF(1-29) — stimulates the pituitary growth hormone-releasing hormone receptor (GHRHR). Together, their combined signal closely replicates the natural GH pulse architecture generated by coordinated GHRH-ghrelin axis activity, making this combination one of the most studied in GH pulse amplification and neuroendocrine research. Klene Peptides supplies this combination to USA research institutions with verified purity and same-day fulfillment.

Every vial from Klene Peptides includes:

Chemical Identity & Structural Profiles

Ipamorelin

Parameter Value
Full Name Ipamorelin
Sequence H-Aib-His-D-2-Nal-D-Phe-Lys-NH₂
Residue Class Growth Hormone Releasing Peptide (GHRP); pentapeptide
Molecular Weight 711.86 g/mol
CAS Number 170851-70-4
Primary Target GHSR-1a (Ghrelin / GH Secretagogue Receptor 1a)
Appearance White lyophilized powder
Storage Lyophilized: −20°C; Reconstituted: 4°C, use within 14–21 days

CJC-1295 Without DAC (Modified GRF 1-29)

Parameter Value
Full Name CJC-1295 without DAC / Modified GRF(1-29) / Mod-GRF(1-29)
Sequence 29-amino acid GHRH(1-29) analog with stabilizing substitutions
Key Substitutions Enhanced DPP-IV resistance at positions 2, 8, 15, 27
Molecular Weight ~3,367 g/mol
CAS Number 863288-34-0
Primary Target GHRHR (Growth Hormone-Releasing Hormone Receptor)
Appearance White lyophilized powder
Storage Lyophilized: −20°C; Reconstituted: 4°C, use within 14–21 days

Key distinction: CJC-1295 with DAC (Drug Affinity Complex) uses a reactive maleimide group to form a covalent bond with serum albumin, extending its half-life to 6–8 days. CJC-1295 without DAC lacks this conjugation, producing a shorter half-life (~30 minutes) that mimics the natural GHRH pulse — the preferred form for pulsatile GH physiology research.

Mechanism of Action

Dual-Receptor Synergy

Component Receptor Signal Effect
Ipamorelin GHSR-1a (ghrelin receptor) Gq/11 → PKC; Gi/o → cAMP reduction Selective GH pulse release; no significant cortisol or prolactin elevation
CJC-1295 No DAC GHRH receptor Gs → adenylate cyclase → cAMP → PKA GH synthesis upregulation; somatotroph cell sensitization
Combined Both GHSR-1a + GHRHR Additive/synergistic intracellular signals Amplified, physiologically-patterned GH pulse

The synergy is mechanistically important: CJC-1295 no DAC stimulates the synthesis and priming of GH in somatotroph cells via the cAMP/PKA pathway, while Ipamorelin simultaneously triggers GH release through the ghrelin receptor’s calcium-dependent exocytosis pathway. The result is a GH pulse of greater amplitude than either peptide alone, without suppressing the hypothalamic-pituitary axis feedback loop.

Selectivity Profile of Ipamorelin

Hormone / Parameter Effect Research Significance
Growth Hormone (GH) Significant elevation Primary endpoint in GH pulse research
IGF-1 Secondary increase (GH-mediated) Tissue anabolic signaling studies
Cortisol No significant increase Distinguishes Ipamorelin from GHRP-2 and GHRP-6
Prolactin No significant increase High selectivity advantage in neuroendocrine research
ACTH No significant increase HPA axis neutrality confirmed
Appetite / Ghrelin Effects Minimal at research doses Functionally distinct from endogenous ghrelin

Pharmacokinetic & ADME Profiles

Ipamorelin

Parameter Value Notes
Route (Research) SC, IV SC preferred for pulsatile studies
Tmax ~15–30 minutes (SC) Rapid peak GH elevation
Half-life (t½) ~2 hours Short-acting; designed for pulsatile stimulation
Bioavailability (SC) >70% (estimated) High subcutaneous absorption
Metabolism Proteolytic (serum and tissue) No CYP450 pathway
Excretion Renal Metabolite clearance

CJC-1295 No DAC

Parameter Value Notes
Route (Research) SC Standard research delivery
Tmax ~5–15 minutes (SC) Rapid receptor engagement
Half-life (t½) ~30 minutes Without albumin conjugation; pulse-appropriate
Bioavailability (SC) >75% (estimated) High subcutaneous absorption
Metabolism DPP-IV resistant vs. native GHRH; proteolytic Modified sequence resists rapid DPP-IV cleavage at Ala²
Excretion Renal Metabolite clearance

Research Applications

GH Pulse Architecture Research

Research Parameter Methodology Observed Outcome
GH Peak Amplitude Serial serum GH measurement post-administration 2–5× baseline GH elevation vs. either peptide alone
Pulse Duration AUC analysis over 2–4 hour windows Extended pulse profile vs. Ipamorelin alone
IGF-1 Response 24-hour serum IGF-1 measurement Dose-dependent sustained elevation
HPA Axis Neutrality ACTH and cortisol co-measurement No significant HPA perturbation

Body Composition & Metabolic Research

Area Mechanism Research Focus
Lean Mass GH/IGF-1 anabolic signaling Muscle protein synthesis rate studies
Adipose Reduction GH-driven lipolysis (visceral and subcutaneous) Fat mass and body composition modeling
Glucose Metabolism GH-mediated insulin sensitivity modulation Metabolic flexibility and HOMA-IR studies

Aging & Somatopause Research

GH secretion declines approximately 1–2% annually after peak in early adulthood (somatopause). This combination is studied to:

Sleep & Circadian Biology

GH secretion is primarily nocturnal and linked to slow-wave sleep. Research protocols examine how GH secretagogue combinations affect:

Research Dosing Reference

For scientific reference only — not prescriptive recommendations

Peptide Reported Dose Range Route Timing
Ipamorelin 100–300 mcg per administration SC Pre-sleep or fasted state
CJC-1295 No DAC 100–300 mcg per administration SC Co-administered with Ipamorelin
Combined (typical research) 100–200 mcg each, combined per injection SC 1–3× daily per protocol design

Dosing ranges derived from published pharmacological and clinical research literature.

Reconstitution Reference

Lyophilized Amount (each peptide) Bacteriostatic Water Concentration
5 mg 2.5 mL 2.0 mg/mL
10 mg 5.0 mL 2.0 mg/mL

Klene Peptides Quality Standards

Certificate of Analysis — Standard Parameters

Every batch supplied by Klene Peptides is verified against the following analytical benchmarks:

Test Specification Method
Purity (both components) ≥99% HPLC (High-Performance Liquid Chromatography)
Molecular Identification Confirmed for each component HPLC-MS (High-Performance Liquid Chromatography – Mass Spectrometry)
Water Content <1.5%

What Every Klene Peptides Order Includes

Ordering Ipamorelin + CJC-1295 (No DAC) for Your Research Program

Important Research Compliance Notice

All products sold by Klene Peptides are strictly for in vitro research and laboratory investigation purposes only. Ipamorelin and CJC-1295 (No DAC) supplied by KlenePeptides.net have not been evaluated by the FDA for human safety or efficacy. They are not approved for human or veterinary administration. Purchase, possession, and use must comply with all applicable federal, state, and local regulations. This content is intended for licensed researchers and qualified scientific personnel only.

Scientific References

© 2026 Klene Peptides | KlenePeptides.net | USA-Based Research Peptide Supplier | For Research Use Only
Scroll to Top