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Ipamorelin

Ipamorelin

CAS #: 170851-70-4

Ipamorelin

Research Use Only

All products are intended solely for laboratory research and are not for human or animal consumption. By purchasing, the buyer agrees to use these products in compliance with all applicable laws.

Ipamorelin Overview

Ipamorelin is a synthetic pentapeptide and selective secretagogue-type agonist. It is studied in preclinical and experimental research for its selective pituitary signaling activity with minimal off-target pathway interference. This selectivity makes it an important tool for investigating endocrine signaling, somatotroph axis modulation, and related molecular pathways.

Svensson J. et al. (1998).

History

Ipamorelin was developed in the 1990s during research into secretagogue-type peptides. Unlike earlier compounds such as GHRP-6, Ipamorelin demonstrated greater selectivity, activating target pathway signaling with minimal off-target interference. Since its discovery, it has been applied in studies investigating pituitary signaling, endocrine cascades, and downstream pathway dynamics in laboratory models.

Bowers C.Y. et al. (1997).

Ipamorelin Structure

CAS #: 170851-70-4

Molecular Formula: C₃₈H₄₉N₉O₅

Molecular Weight: 711.9 g/mol

PubChem ID: 9831659

Research Findings

Ipamorelin has been studied in endocrine, metabolic, and regenerative models, with research highlighting its activity in stimulating growth hormone release, modulating IGF-1 pathways, and supporting tissue recovery processes. Studies have also examined its role in metabolic regulation, energy balance, and cellular repair in preclinical systems.

Key Areas of Research:

  • Endocrine: Somatotroph axis, signaling, cascades

  • Signaling: Systemic markers, pathway dynamics

  • Molecular: Remodeling, proliferation, viability

Together, these findings suggest experimental utility for Ipamorelin across multiple biological pathways. By influencing endocrine signaling and downstream remodeling processes, Ipamorelin provides a versatile platform for research into pathway dynamics, endocrine activity, and systemic resilience in laboratory settings.

Raun K. et al., 1998

References

Svensson J. et al. (1998). Ipamorelin selectively stimulates GH release in humans without affecting cortisol or prolactin. J Clin Endocrinol Metab, 83(9):3094–3101. 

Bowers C.Y. et al. (1997). Ipamorelin: a novel pentapeptide GH secretagogue. Endocrinology, 138(9): 4011–4016. 

Culler M.D. et al. (2002). Pharmacological characterization of Ipamorelin, a GHRP with GH selectivity. J Endocrinol, 174(2):R1–R6. 

Our Process

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STEP 1

Precision Lyophilization

Manufactured in a controlled U.S. facility under strict compounding standards.

STEP 2

Verified Purity

Every batch third-party tested with HPLC and mass spectrometry.

STEP 3

Same-Day Fulfillment

Orders dispatched same-day from our U.S. facility.

STEP 1

Precision Lyophilization

Manufactured in a controlled U.S. facility under strict compounding standards.

STEP 2

Verified Purity

Every batch third-party tested with HPLC and mass spectrometry.

STEP 3

Same-Day Fulfillment

Orders dispatched same-day from our U.S. facility.
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Frequently Asked Questions

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Each vial contains exactly what’s shown on the label. For example, a 10mg vial has exactly 10mg of lyophilized peptide. Researchers can divide it into smaller portions—like four 2.5mg measurements—but the total amount remains 10mg.

Peptides are supplied as lyophilized powder. They do not come reconstituted, and any extra supplies must be sourced separately for research applications.
In lyophilized powder form, peptides stay stable for up to 2 years. After reconstitution, it should be refrigerated and is generally stable for up to 2 months.

Products from Raw Peptides do not include usage instructions, as they are strictly for in vitro research and prohibited by law for human or animal use. Misuse or unlawful application will result in permanent denial of service.

Lyophilized peptides should be stored away from heat and light. Once reconstituted, they must be refrigerated to maintain stability and efficacy.