Ipamorelin

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Ipamorelin is a synthetic pentapeptide with the sequence Aib-His-D-2-Nal-D-Phe-Lys, first described in the mid-1990s and developed specifically to improve on earlier growth hormone secretagogues like GHRP-6, which carried more pronounced effects on cortisol, prolactin, and appetite. Ipamorelin’s structure, built around two non-standard amino acids, aminoisobutyric acid (Aib) and D-2-naphthylalanine (D-2-Nal), gives it unusually high selectivity for the ghrelin/GHS receptor, making it one of the most receptor-selective compounds in this class. It has the molecular formula C38H49N9O5, molecular weight 711.86 g/mol, CAS 170851-70-4. Supplied as a white to off-white lyophilized powder. This product is strictly for research purposes only.

ℹ️ Note: 1 kit includes 10 vials

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Description

Ipamorelin is a synthetic pentapeptide, sequence Aib-His-D-2-Nal-D-Phe-Lys, molecular formula C38H49N9O5, molecular weight 711.86 g/mol, CAS 170851-70-4, first described in the mid-1990s, classified as a growth hormone secretagogue (GHS).

Structurally, Ipamorelin contains two non-standard amino acids: aminoisobutyric acid (Aib) at the N-terminus and D-2-naphthylalanine (D-2-Nal) in the third position. These modifications were specifically engineered to improve receptor selectivity over earlier-generation secretagogues like GHRP-6, which activates the ghrelin/GHS receptor but also produces more pronounced secondary effects on cortisol, prolactin, and appetite. Published pharmacology research has consistently reported that Ipamorelin stimulates GH release with a cleaner secondary hormone profile than these earlier compounds, which is why it’s frequently selected as the ghrelin-receptor component in combination protocols, most notably paired with CJC-1295 in research settings.

In its research-grade form, Ipamorelin appears as a white to off-white lyophilized powder that dissolves readily in water. This product is strictly for research purposes only.

PubChem Reference: View compound profile on NIH PubChem

Key Characteristics

MOLECULAR PROFILE

Formula: C38H49N9O5

Weight: 711.86 g/mol

CAS: 170851-70-4

Structure: Aib-His-D-2-Nal-D-Phe-Lys

PHYSICAL PROPERTIES

Form: White to off-white lyophilized powder

Solubility: Readily dissolves in water

Selectivity: High receptor selectivity

Storage: Keep refrigerated 36‑46 °F (2‑8 °C)

Ipamorelin in Published Research

Ipamorelin’s research value comes largely from its selectivity: published studies comparing it to older secretagogues report GH release with minimal impact on cortisol, prolactin, or appetite, effects that are much more pronounced with GHRP-6 or GHRP-2. This selectivity profile is why it’s become the standard ghrelin-receptor-pathway compound researchers pair with GHRH analogs like CJC-1295 when studying additive, receptor-complementary GH release.

Frequently Asked Questions :

What is Ipamorelin studied for?

Growth hormone secretagogue research, valued for its receptor selectivity compared to earlier GHRPs.

How is it different from GHRP-2 and GHRP-6?

All three are ghrelin-receptor agonists, but Ipamorelin was engineered for greater selectivity, minimizing cortisol, prolactin, and appetite effects seen with the older compounds.

Why is it often paired with CJC-1295?

The two act on different receptors (ghrelin vs. GHRH), providing additive, mechanistically distinct GH-release research value.

How should it be reconstituted and stored?

Bacteriostatic water, refrigerate 2–8°C.

Where can I buy it?

5mg and 10mg kits, HPLC/MS verified.

Additional information

Weight

5mg, 10mg

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