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⚑ Growth Hormone CAS: 170851-70-4 βœ“ 99%+ Purity

Ipamorelin
Selective Growth Hormone Secretagogue

β˜…β˜…β˜…β˜…β˜…4.8 / 5  Β·  Most selective GHRP available

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$69
5mg
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99%+ purity, independently verified by HPLC & mass spectrometry
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Lyophilized vials β€” shipped with cold pack, stable at βˆ’20Β°C long term
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⚠️ For Research Use Only. Ipamorelin is not approved for human consumption or therapeutic use. This product is sold exclusively as a research chemical for in vitro and laboratory research only.

What is Ipamorelin?

Ipamorelin is a pentapeptide (Aib-His-D-2-Nal-D-Phe-Lys-NHβ‚‚) that acts as a selective agonist of the ghrelin/growth hormone secretagogue receptor (GHS-R). Unlike GHRP-2 and GHRP-6, ipamorelin does not significantly stimulate cortisol, prolactin, or ACTH, making it the cleanest GHRP available for isolated GH pulse research.

CAS 170851-70-4 | MW 711.9 Da

GHS-R1a Agonism

Binds selectively to the ghrelin receptor (GHS-R1a) in the pituitary and hypothalamus, triggering pulsatile GH release.

Clean Selectivity

Studies show ipamorelin does not raise cortisol, prolactin, or ACTH at research doses β€” unique among GHRPs.

Synergy with CJC-1295

Combined with GHRH analogues like CJC-1295, ipamorelin produces amplified GH pulses via dual receptor stimulation.

Pulsatile Release

Mimics physiological GH secretion pattern, preserving negative feedback loops and avoiding receptor downregulation.

Selectivity vs GHRP-2 and GHRP-6

Raun et al. (1998) demonstrated that ipamorelin stimulated GH release at equivalent potency to GHRP-6 in rats, but without the ACTH or cortisol response seen with GHRP-2 and GHRP-6, establishing ipamorelin as the first truly selective GHRP.

Eur J Endocrinol. 1998;139(5):552–561

Bone Density Research

Svensson et al. found ipamorelin increased bone mineral density in ovariectomized rats after 12 weeks of treatment, suggesting potential applications in bone metabolism research.

Growth Horm IGF Res. 2000;10(5):266–272

GH/IGF-1 Axis Modulation

Multiple rodent studies confirm ipamorelin reliably elevates both GH and downstream IGF-1 levels in a dose-dependent manner, supporting its use as a tool compound for GH axis research.

J Endocrinol. 1999;163(3):487–495

Published Research Dosing Protocols

In rodent studies, ipamorelin has been administered at 200–300 Β΅g/kg subcutaneously. In primates and clinical pilot work, doses between 30–300 Β΅g per injection have been investigated. Protocols typically examine 1–3 injection timing windows per day to correlate with natural GH pulse patterns.

Reconstitution: Bacteriostatic water is used in published protocols. Storage at βˆ’20Β°C after reconstitution for research stability.
Full NameIpamorelin
CAS Number170851-70-4
Molecular FormulaCβ‚ƒβ‚ˆH₄₉N₉Oβ‚…
Molecular Weight711.9 Da
SequenceAib-His-D-2-Nal-D-Phe-Lys-NHβ‚‚
Purityβ‰₯99% by HPLC
AppearanceWhite lyophilized powder
Storageβˆ’20Β°C, desiccated
FormatLyophilized vials