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≥99% PurityCJC / IPA Blend vial

CJC / IPA Blend

Two-peptide blend · GHRH-R and GHS-R pathways

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About this compound

This blend pairs CJC-1295 with ipamorelin. Both relate to growth hormone, but they act at different receptors. CJC-1295 copies GHRH, the hormone that signals release. Ipamorelin acts at a separate receptor called GHS-R. Research has measured what happens when both are present compared to either one alone. Pairing a GHRH analog with a secretagogue is a common combination in growth hormone research.

Dual-component blend: GHRH-R agonist (CJC-1295, Modified GRF 1-29) + GHSR-1a agonist pentapeptide (Ipamorelin)

Formula
BLEND
Form
Lyophilized Powder (co-lyophilized blend)
Purity
>99% (HPLC)
Vial size
10mg
Read the full CJC / IPA Blend research monograph
0 Pathways
Dual-Receptor Action
GHRH-R + GHSR-1a simultaneous activation
0%
Cortisol Elevation
Ipamorelin selectivity preserved in blend
0%
Prolactin Elevation
No prolactin co-secretion vs GHRP-6
0
Research Areas
Dual-Pathway GH Response · Secretion Patterns · Selectivity vs GHRP-6 Blends & more
How It Works

How CJC / IPA Blend works

The pathways CJC / IPA Blend acts on — and what each one does. The animation traces its signal outward from the compound to every target it engages.

Signalling pathways studied in preclinical models · illustrative
CJC-1295: GHRH Receptor Activation
GHRH-R Pathway

CJC-1295 (Modified GRF 1-29) is the GHRH receptor agonist component. It binds GHRH-R on pituitary somatotrophs, with cAMP production and GH synthesis measured. The four DPP-IV-resistant amino acid substitutions extend bioavailability to ~30 minutes, giving a longer window of GHRH-R activation per administration.

  • GHRH-R agonism — cAMP-mediated GH synthesis
  • ~30-minute half-life for time-matched dosing
  • Cortisol, thyroid, prolactin unaffected
Ipamorelin: Ghrelin Receptor Activation
GHSR-1a Pathway

Ipamorelin is the GHSR-1a (ghrelin receptor) agonist component. It binds a distinct receptor population on somatotrophs via a phospholipase C / IP3 intracellular pathway — separate from the cAMP route used by GHRH. This complementary signaling allows both pathways to be active simultaneously without receptor competition.

  • GHSR-1a agonism — PLC/IP3 intracellular pathway
  • No cortisol, ACTH, or prolactin co-secretion
  • ~2-hour half-life — pulsatile GH release
Dual-Pathway Synergistic GH Amplification
Synergy

When GHRH-R and GHSR-1a are activated simultaneously, GH pulse amplitude above either compound alone has been recorded. Preclinical data describe an additive interaction between the two pathways at the pituitary.

  • Additive GH pulse amplitude vs either alone
  • Somatostatin suppression potentiated by GHSR agonism
  • Physiologic pulsatile pattern preserved
Uses & Applications

What CJC / IPA Blend is researched for

The main areas CJC / IPA Blend is being studied for — and the study-reported figures behind them.

GH Axis Research

Dual-Pathway GH Response

Simultaneous GHRH-R and GHSR-1a activation produces additive GH pulse amplification — a model for studying maximal pituitary GH secretory capacity while maintaining physiologic pulse architecture.

Pulsatile GH Dynamics

Physiologic Secretion Patterns

The short half-lives of both components (~30 min for CJC-1295; ~2 hr for ipamorelin) preserve pulsatile GH release — enabling research into GH pulse physiology without continuous baseline elevation.

Endocrinology

Selectivity vs GHRP-6 Blends

CJC-1295/Ipamorelin is studied as a higher-selectivity comparator to CJC-1295/GHRP-6 combinations — GH response amplitude is retained while cortisol and prolactin co-secretion associated with GHRP-6 is absent.

Receptor Pharmacology

Complementary Signaling Pathways

GHRH-R signals via cAMP/PKA while GHSR-1a signals via PLC/IP3 — distinct second messenger cascades that do not compete. This orthogonal mechanism makes the combination a research model for studying receptor cross-talk in neuroendocrine signaling.

Study-reported magnitudes

Representative figures from published research. Bars fill as you scroll.

GH Pulse Amplitude (dual-pathway vs single)Additive
Cortisol Elevation (ipamorelin component)None
Prolactin Elevation (ipamorelin component)None
GHRH-R / GHSR-1a Receptor SelectivityHigh

Figures are representative of published research findings and shown for reference.

Molecular Structure

The CJC / IPA Blend molecule

An interactive 3D model rendered from the compound record — rotate and explore its structure.

BLEND

Molecular formula
BLEND
Sequence length
blend
Physical form
Lyophilized Powder (co-lyophilized blend)
Documented purity
≥99% by HPLC
How Long It Lasts

Duration & clearance

How CJC / IPA Blend clears from circulation, modeled from its documented ~~20–30 minutes half-life. The curve draws as you scroll.

CJC / IPA Blend · ~~20–30 minutes
Reference · rapid clearance
Compound Information

Full specification

Strength10mg
Molecular FormulaBLEND
Molecular WeightN/A (Blend)
Purity>99% (HPLC)
FormLyophilized Powder
Blend ComponentsCJC-1295 (Modified GRF 1-29) + Ipamorelin
CJC-1295 TypeGHRH analog — GHRH-R agonist (no DAC modification)
Ipamorelin TypePentapeptide GH secretagogue — GHSR-1a agonist
CJC-1295 MW3,367.9 g/mol
Ipamorelin MW711.9 g/mol
CJC Half-Life~20–30 minutes
Ipamorelin Half-Life~2 hours
FormLyophilized powder (co-lyophilized blend)
Purity≥99% each component (HPLC verified)
TestingThird-party HPLC, Mass Spec, Endotoxin
Storage-20°C for up to 24 months
SolubilityWater-soluble
COAIncluded with every order
AppearanceWhite to off-white powder
FAQ

Common questions about CJC / IPA Blend

The CJC-1295/Ipamorelin blend combines two peptides acting on pituitary GH release through distinct receptor systems. CJC-1295 (Modified GRF 1-29) activates GHRH receptors (GHRH-R) via the cAMP/PKA intracellular pathway. Ipamorelin activates GHSR-1a (ghrelin receptors) via the PLC/IP3 pathway. Because these are separate receptor populations using different second messenger systems, simultaneous activation has been recorded producing larger GH pulses than either alone, without receptor competition.

Both ipamorelin and GHRP-6 are GHSR-1a agonists, but ipamorelin is more selective. GHRP-6 co-elevates cortisol, ACTH and prolactin — stress and pituitary hormones that confound research readouts. Ipamorelin gives a comparable GH response without those confounders, which is why the CJC-1295/Ipamorelin combination is used where cortisol and prolactin need to be excluded as variables.

Pulsatile GH secretion means GH is released in discrete bursts rather than a steady continuous stream. Endogenously, this occurs 6–12 times per day, with the largest pulses during slow-wave sleep. The pulsatile pattern is important because GH receptor sensitivity, downstream IGF-1 production, and metabolic effects all depend on the pulse amplitude and inter-pulse interval. CJC-1295/Ipamorelin preserves this pulsatile architecture (due to short half-lives) — making it a tool for studying GH pulse physiology rather than pharmacological continuous GH replacement.

The combination has not been characterised as a single formulation. The rationale is derived from: (1) ipamorelin pharmacology describing GHSR-1a selective GH stimulation; (2) CJC-1295 pharmacokinetic characterisation describing GHRH-R-mediated GH/IGF-1 elevation; and (3) preclinical work describing additive GH responses when GHRH and GH secretagogues are co-administered.

No. Neither CJC-1295 without DAC nor ipamorelin is FDA-approved for any indication, and the combination has no regulatory approval. Both are research compounds classified as not intended for human therapeutic use. This blend is sold exclusively for in vitro research purposes.

The lyophilized powder blend should be stored at -20°C for long-term stability. Avoid repeated freeze-thaw cycles and protect from light. Both components maintain stability in lyophilized form; CJC-1295 is relatively more sensitive to DPP-IV degradation in solution due to the absence of albumin binding.

Research Use Only.

Not for human or veterinary use. For in-vitro laboratory research only. These statements have not been evaluated by the FDA; this product is not intended to diagnose, treat, cure, or prevent any disease. Sold exclusively to qualified researchers and institutions.