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Ipamorelin 10mg

Ipamorelin 10mg

Ipamorelin is a pentapeptide growth hormone secretagogue and selective ghrelin receptor (GHS-R1a) agonist, studied for its highly specific stimulation of growth hormone release without measurable effect on cortisol or prolactin. Supplied as a ≥99% HPLC-verified lyophilized powder for laboratory research use only.

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Third-Party Tested

Certificate of Analysis

Third-Party Tested by Janoshik Analytical

Latest
N/A%
Purity
Variant
Ipamorelin 10mg
Lot #
IP102607
Labeled
Ipamorelin
Actual
N/A
Tested
Jul 17, 2026
View Certificate
Latest
99.685%
Purity
Variant
Ipamorelin 10mg
Lot #
IP102607
Labeled
Ipamorelin
Actual
N/A
Tested
Jul 7, 2026
View Certificate
Latest
N/A%
Metal
Variant
Ipamorelin 10mg
Lot #
KL802607
Labeled
KLOW
Actual
N/A
Tested
Jul 8, 2026
View Certificate
Latest
N/A%
Endotoxins
Variant
Ipamorelin 10mg
Lot #
IP102607
Labeled
Ipamorelin
Actual
N/A
Tested
Jul 1, 2026
View Certificate

Compound Information

Technical specifications

Molecular Profile

What Is Ipamorelin?

TypePentapeptide GHS (Selective GHS-R1a Agonist)
CAS Number170851-70-4
Molecular Weight711.85 g/mol
SynonymsNNC 26-0161 / Ipamorelin Acetate
Amino Acids5 AA (pentapeptide)
SequenceAib-His-D-2-Nal-D-Phe-Lys-NH2
FormulaC38H49N9O5
Storage Requirements

Stability Information

Lyophilized powder; keep sealed, dry, and protected from light
Store at a stable temperature; minimize warming/cooling cycles
Aliquot after reconstitution; avoid repeated freeze–thaw cycles

Lyophilized Powder

-20°C preferred; 2–8°C for short-term handling

Reconstituted

2–8°C

About Ipamorelin

Ipamorelin is a synthetic pentapeptide growth hormone secretagogue that acts as a selective agonist at the ghrelin receptor (GHS-R1a) in the pituitary. What distinguishes it from earlier secretagogues such as GHRP-6 and GHRP-2 is its selectivity: in the studies that established its profile, it triggered growth hormone release without the accompanying rise in cortisol, prolactin, or ACTH seen with less selective compounds, and without the appetite stimulation associated with strong ghrelin agonism. That clean signal is why it remains a standard reference compound in GH-axis research — investigators can attribute observed downstream effects to GH itself rather than to confounding hormonal noise. It is frequently paired with a GHRH analog such as CJC-1295 No-DAC in study designs exploring synergistic pituitary stimulation, since the two act through complementary receptor pathways. Supplied as a high-purity lyophilized powder for reproducible in-vitro and approved in-vivo work. This product is for laboratory research and development purposes only and must be handled by qualified professionals. Not for human, therapeutic, or diagnostic use.

Research Highlights

Receptor Selectivity

A selective GHS-R1a agonist — stimulating GH release without the cortisol, prolactin, or ACTH elevation seen with earlier GHRPs.

Clean Signal Profile

Minimal off-target hormonal activity lets researchers attribute downstream effects to GH itself rather than confounding variables.

Complementary Pathway

Acts through the ghrelin receptor rather than the GHRH receptor — commonly paired with GHRH analogs in synergy studies.

Compact Pentapeptide

Just five residues with a C-terminal amide — a short, stable structure that is straightforward to synthesize and characterize.

GH–IGF-1 Axis Studies

A reference secretagogue for investigating pituitary response and downstream IGF-1 signaling in controlled study models.

≥99% HPLC Purity

Every batch is HPLC-verified and supplied lyophilized, ensuring reproducible results across long study timelines.

Product Specifications

Molecular Formula
C38H49N9O5
Molecular Weight
711.85 g/mol
CAS Number
170851-70-4
Sequence
Aib-His-D-2-Nal-D-Phe-Lys-NH2
Purity
≥99% (HPLC verified)
Form
Lyophilized powder
Appearance
White to off-white powder
Solubility
Soluble in water, bacteriostatic water
Storage
-20°C (lyophilized), 2–8°C (reconstituted)

Research Studies

Frequently Asked Questions

What is Ipamorelin?

Ipamorelin is a synthetic pentapeptide growth hormone secretagogue that acts as a selective agonist at the ghrelin receptor (GHS-R1a), stimulating growth hormone release from the pituitary.

How does Ipamorelin differ from GHRP-2 and GHRP-6?

Its defining feature is selectivity. Where earlier GHRPs also elevate cortisol, prolactin, and ACTH, Ipamorelin was characterized as producing GH release without those off-target hormonal responses.

Why is it often studied alongside a GHRH analog?

Ipamorelin acts at the ghrelin receptor while GHRH analogs such as CJC-1295 No-DAC act at the GHRH receptor. Because the pathways are complementary, the pairing is a common design in studies investigating synergistic pituitary stimulation.

Is this product approved for human use?

No. This product has not been evaluated by the FDA and is strictly intended for research and development purposes by qualified professionals only.

Ipamorelin molecular structure

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