Skip to content

Ipamorelin

Identification

Property Value
CAS Number 170851-70-4
Molecular Formula C₃₈H₄₉N₉O₅
Molecular Weight ~711.9 Da
Sequence Aib-His-D-2-Nal-D-Phe-Lys-NH₂
Amino Acid Count 5 (Aib¹, D-2-Nal³, D-Phe⁴ modified)
Appearance White to off-white lyophilized powder
Purity Standard ≥99% by HPLC
Solubility Soluble in sterile or bacteriostatic water
Storage 2–8°C, desiccated, protect from light

Category: Muscle Growth

Catalog SKU: PSH-IPAM-2MG

Research Background

Ipamorelin is a synthetic pentapeptide GH secretagogue that selectively activates the ghrelin receptor (GHS-R1a). What distinguishes it from earlier GHS peptides is receptor selectivity — it produces a clean GH pulse with minimal activation of ACTH/cortisol, prolactin, or hunger-signaling pathways. This selectivity is achieved through strategic incorporation of non-proteinogenic amino acids: Aib at position 1, D-2-Nal at position 3, and D-Phe at position 4.

Key Mechanisms

Mechanism Details
GHS-R1a Agonism Selective ghrelin receptor activation on pituitary somatotrophs → GH release
Somatostatin Suppression GHS-R activation reduces hypothalamic somatostatin tone → permissive GH secretion
Minimal Off-Target Unlike GHRP-2/GHRP-6, Ipamorelin does not significantly activate ACTH/cortisol or hunger pathways

Research Focus Areas

Selective GH Release

Clean GH pulse with minimal prolactin, ACTH, or cortisol elevation

GH Secretagogue Research

GHS-R1a pharmacology — receptor selectivity profiling

Body Composition

Lean mass preservation in caloric deficit models

Combination Protocols

Synergistic GH elevation with GHRH analogues (CJC-1295)

Available Configurations

Configuration Content Best For
Standard Kit 2 mg × 10 vials GH pulse studies; evaluation
Bulk Kit 5 mg × 10 vials Chronic protocols; repeat orders
Custom Custom mg × custom vials OEM; private-label

Tiered Wholesale Pricing

Volume Discount For
1 kit List price Evaluation; competitive analysis
5+ kits 10% off Initial portfolio expansion
20+ kits 20% off Mid-size distributors
50+ kits 30% off Regional distributors

Quality Specifications

Parameter Method Criterion
Purity HPLC at 214 nm, C18 column ≥99.0% peak area
Identity (MW) ESI-MS ~711.9 ± 1.0 Da
Appearance Visual inspection White to off-white powder
Chiral Purity Chiral HPLC ≥99% (Aib, D-2-Nal, D-Phe verified)
Residual Moisture Karl Fischer ≤3%

Frequently Asked Questions

Q1: What makes Ipamorelin different from GHRP-2/GHRP-6?

Selectivity. Ipamorelin is the most selective ghrelin receptor agonist of the GHRP family. At research concentrations, it produces GH release without significant ACTH, cortisol, prolactin, or hunger elevation. GHRP-2/6 are more potent GH releasers but with broader receptor profiles.

Q2: Why is Ipamorelin paired with CJC-1295?

CJC-1295 provides the GHRH signal (the 'on' switch). Ipamorelin suppresses somatostatin tone (the 'off' switch). Together they produce synergistic GH pulse — the most studied GH secretagogue protocol in preclinical research.

Q3: What are the unique amino acid modifications?

Aib (α-aminoisobutyric acid) at position 1 for protease resistance; D-2-Nal at position 3 for GHS-R binding selectivity; D-Phe at position 4 to further refine selectivity. Confirmed by chiral HPLC in every batch.

Q4: How does Ipamorelin affect appetite vs GHRP-6?

Minimally. GHRP-6 is a potent ghrelin mimetic that strongly activates hunger signaling. Ipamorelin was specifically designed to reduce this off-target effect while maintaining GH release.

Q5: What purity and QC documentation is provided?

≥99% HPLC purity, ESI-MS identity, and chiral HPLC verification of D-amino acid content. Batch-specific COA included.

Key Research References

Reference PMID Key Finding
Raun K et al. "Ipamorelin, the first selective growth hormone secretagogue." Eur J Endocrinol. 1998;139(5):552–561. 9849822 Ipamorelin characterized as the most selective GHS-R1a agonist; produces clean GH pulse with minimal ACTH/cortisol, prolactin, or hunger activation
Johansen PB et al. "Ipamorelin, a new growth hormone secretagogue, increases longitudinal bone growth in rats." Growth Horm IGF Res. 1999;9(2):106–113. 10373343 Ipamorelin increased GH pulsatility and longitudinal bone growth in rodent models, demonstrating anabolic effects of selective GHS-R agonism

Stability & Storage

Condition Degradation Profile
Lyophilized Storage 24 months at 2–8°C in desiccated environment, protect from light
Non-Proteinogenic Amino Acids Aib¹, D-2-Nal³, and D-Phe⁴ provide protease resistance and enhanced solution stability
Neutral pH (6.0–7.5) Stable; recommended for reconstitution in sterile or bacteriostatic water
Reconstituted Solution 24 h at 2–8°C; aliquot and freeze at −20°C. Modified amino acids provide good solution stability. Avoid freeze-thaw cycles

Source & Purchase

For research-grade IPAMORELIN and related compounds in this category, visit the PeptideSourceHub category page for bulk pricing and available specifications.

Browse IPAMORELIN & Related Products →

Product Link
CJC-1295 (no DAC) cjc-1295-no-dac.md — Pulsatile GHRH analogue
CJC-1295 (DAC) cjc-1295-dac.md — Long-acting GHRH analogue
GHRP-2 (Pralmorelin) ghrp-2.md — Potent ghrelin receptor agonist
HGH (Somatropin) hgh.md — 191-aa human growth hormone