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 →
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 |