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Not evaluated by SAHPRA · For information & research use only · Not intended to diagnose, treat, cure or prevent any disease · Consult a healthcare professional
This product has not been evaluated by SAHPRA. For information purposes only — not intended to diagnose, treat, cure or prevent any disease.
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Ipamorelin
PerformanceResearch vialGH secretagogueGHS-R1aselectiverecoverystack

Ipamorelin

Selective GH release without the cortisol spike

R 520
5mg vial
1
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Selective GH releaseTriggers a clean pulsatile GH response with EC50 around 1.3 nmol/L at GHS-R1a.
No cortisol or prolactinEven at 200× the GH ED50, Ipamorelin does not raise ACTH or cortisol above baseline GHRH.
Stacks cleanly with GHRH analogsCommonly paired with CJC-1295 or Tesamorelin for additive dual-receptor GH release.
Recovery and body compositionUsed in research for sleep quality, lean-mass support and post-training recovery via the GH / IGF-1 axis.
Ipamorelin is a pentapeptide (Aib-His-D-2-Nal-D-Phe-Lys-NH2) and a selective agonist of the growth-hormone-secretagogue receptor (GHS-R1a), the same receptor targeted by ghrelin. It triggers pulsatile GH release without the ACTH, cortisol and prolactin spikes seen with older GHRPs (GHRP-2, GHRP-6, hexarelin).
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A two-peptide blend pairing the GHRH analog CJC-1295 (without DAC / Modified GRF 1-29) with the selective ghrelin-receptor agonist Ipamorelin. CJC-1295 lifts the baseline of pulsatile GH release; Ipamorelin amplifies pulse amplitude without driving cortisol, prolactin or ACTH. Dual-receptor stimulation produces a GH response greater than the sum of either alone.

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Hexarelin
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Hexarelin

Hexarelin is a synthetic hexapeptide analog of GHRP-6 and a potent agonist of the growth-hormone-secretagogue receptor (GHS-R1a). It also binds the non-GHS-R receptor CD36, which underlies a separate cardiac action that does not depend on GH release. Of the older GHRPs it produces the strongest GH pulse.

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IGF-1 LR3
1mg vial

IGF-1 LR3

IGF-1 LR3 (Long R3 IGF-1) is an 83-amino-acid synthetic analog of insulin-like growth factor 1 with a 13-residue N-terminal extension and an arginine substituted for glutamic acid at position 3. The Arg-3 substitution drops affinity for IGF binding proteins ~100-fold while preserving full IGF-1 receptor agonism, so more of the injected peptide is free to bind tissue.

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Distributor
Elegant Slimming · Mokopane, Limpopo, South Africa
WhatsApp 076 547 8764 · Mon–Sat 9–5
Regulatory
This product has not been evaluated by the South African Health Products Regulatory Authority (SAHPRA).
For information purposes only — not intended to diagnose, treat, cure or prevent any disease.