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Sermorelin Acetate
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Safety data sheet

Standardized safety protocols and material specifications for professional use.

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Certificate of Analysis

Purity verified via High-Performance Liquid Chromatography (HPLC) for #myo-sermorelin-acetate-5mg

Official Product Data Sheet

Sermorelin Acetate (5mg)

Research Grade >99.4% Purity

Vial Contents
5 mg Sermorelin Acetate — GHRH(1–29) analog (lyophilized powder)
Includes
3 ml bacteriostatic water for reconstitution
Form
Freeze-dried white powder
Purity
≥99%, third-party confirmed (COA available)
Sequence
Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH₂
Molecular Formula
C149H246N44O42S
Molecular Mass
3357.9 g/mol
CAS No.
86168-78-7
Solubility
Reconstitutes readily in bacteriostatic water to ~1.67 mg/mL
Storage
Lyophilized refrigerated at 2–8 °C; reconstituted refrigerated at 2–8 °C for up to 10–14 days

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Scientific Background

Sermorelin is a synthetic 29-amino-acid peptide representing the biologically active N-terminal fragment of endogenous Growth Hormone-Releasing Hormone (GHRH). It is the shortest GHRH fragment that retains full binding affinity and biological activity at GHRH receptors on pituitary somatotrophs, making it the most clinically validated GHRH analog in research.

Sermorelin binds GHRH receptors to activate adenylate cyclase, elevate intracellular cAMP, and trigger pulsatile GH secretion from anterior pituitary somatotrophs. Critically, unlike exogenous recombinant GH (rhGH), Sermorelin preserves the natural GH feedback axis — somatostatin and IGF-1 continue to regulate GH release, preventing runaway GH elevation and maintaining physiological pulsatility. This makes Sermorelin considerably safer and more physiologically appropriate than direct GH administration for research protocols requiring GH axis stimulation.

Originally FDA-approved for paediatric GH deficiency (Geref®), Sermorelin is extensively studied in adults for age-related GH decline, body composition improvement, sleep quality enhancement, and metabolic support. Its bedtime administration leverages the natural nocturnal GH pulse — peak GH secretion occurs during slow-wave sleep — for maximum physiological relevance.

Intended Research Use

  • GHRH receptor pharmacology and pulsatile GH stimulation research
  • Age-related GH decline restoration studies
  • Body composition — lean mass and fat mass studies via GH/IGF-1 axis
  • Sleep quality and slow-wave sleep GH pulse research
  • Paediatric GH deficiency models (GHRH analog)
  • Comparative GHRH/GHRP combination pharmacology
warning

FOR RESEARCH USE ONLY. This product is intended for laboratory research purposes only and is not for human consumption, medical, or diagnostic use.

Myotrope

Possible stacks with other peptides

Synergistic combinations for enhanced research outcomes

Sermorelin is most powerful when combined with GHRPs that provide complementary pituitary stimulation via ghrelin receptor pathways.

schedule

Cycling Note: Protocols typically run 3–6 months minimum. Monitor IGF-1 at 4–6 week intervals to guide dose titration. Allow 4-week rest between extended cycles.