NOTE:
You can purchase bacteriostatic water here:
BAC 10ml BAC 30ml
Ipamorelin is a synthetic pentapeptide and selective growth hormone releasing peptide (GHRP) that stimulates the pituitary to release growth hormone in a pulsatile, physiologically consistent manner.
Preclinical research identifies the ipamorelin peptide as the first GHRP to produce a clean GH release profile with minimal impact on cortisol, ACTH, and prolactin, a characteristic that separates it from earlier secretagogues.
Size / Amount:
Ipamorelin vials must be stored in a cool, dry place away from direct sunlight. Unreconstituted ipamorelin peptide should be kept at -20°C for long-term storage or 2-8°C for short-term storage. Once reconstituted with bacteriostatic water, ipamorelin should be refrigerated at 2-8°C and used within 28-30 days for optimal stability. Do not freeze reconstituted solutions. Always follow proper aseptic technique and storage guidelines to maintain product integrity for research applications.
Ipamorelin is freely soluble in bacteriostatic water and sterile saline. Gently swirl the vial after adding solvent. Do not vortex or shake vigorously, as this may damage the peptide structure.
Ipamorelin is intended for research purposes only and is not approved for human use.
Ipamorelin dosage per day used in preclinical research varies by study design, animal model, and adminisration route. Common protocols in published literature include:
Ipamorelin dosage and timing in research protocols often aligns administration with periods of fasting or rest cycles to maximize GH pulse amplitude, consistent with the natural relationship between feeding state and GH secretion dynamics. A peptide calculator can help scale published mcg/kg doses to a given research subject weight.
When CJC-1295 and ipamorelin are studied together, matched concentrations of both peptides are administered together, leveraging synergistic GH release from their complementary receptor targets, with CJC-1295 acting on the GHRH receptor and ipamorelin acting on the GHS-R (ghrelin receptor).
This product is intended for research purposes only and should not be used for human consumption. It is strictly designated for laboratory and scientific use by qualified professionals. Common research applications include:
Raun et al. characterized ipamorelin as the first GHRP to demonstrate a highly selective growth hormone release profile. In rat studies, ipamorelin produced a dose-dependent GH pulse comparable in magnitude to GHRP-6 and GHRP-2 while producing no statistically significant elevation in ACTH, cortisol, aldosterone, or prolactin, even at doses up to 500 mcg/kg. The authors concluded that ipamorelin's clean selectivity profile distinguishes it from all previously described GHRPs, establishing it as a uniquely characterized GH secretagogue for preclinical research.
Johansen et al. demonstrated that ipamorelin administered to young rats over a 2-week period produced significant, dose-dependent increases in tibia length, body weight, and growth velocity. Effects were comparable to exogenous growth hormone treatment in matched controls, confirming that ipamorelin's downstream anabolic signaling through the GH/IGF-1 axis is sufficient to drive measurable skeletal and somatic growth. The findings support ipamorelin peptide's research value as a potent GH secretagogue for bone and body composition studies.
Bowers et al. demonstrated that co-administration of a growth hormone-releasing peptide (GHRP) with GHRH produces a synergistic GH pulse that substantially exceeds what either compound achieves independently. The study identified the dual-receptor mechanism underlying modern GHRP/GHRH combination protocols: simultaneous activation of the ghrelin receptor (by GHRPs such as ipamorelin) and the GHRH receptor (by analogs such as CJC 1295) amplifies GH release well beyond additive effects. This foundational finding provides the scientific rationale for the widely studied CJC-1295 ipamorelin combination in current peptide research.
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