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Compound research hub

Sermorelin: Research, Handling and Batch Documentation

Sermorelin is GHRH(1-29) amide, the shortest fragment of growth-hormone-releasing hormone that retains full activity, and the only compound in this area to have held a human marketing authorisation.

Part of Volta's growth hormone research peptides catalogue.

Identity and research status

Also referred to as
GRF 1-29, Geref, Gerel, Sermorelin Acetate
Sequence
Residues 1 to 29 of human GHRH, C-terminally amidated
Molecular Formula
C149H246N44O42S
Molecular Weight
3357.93 g/mol
CAS Number
86168-78-7
Length
29 amino acids
Also Known As
GRF(1-29) amide, GHRH(1-29)NH2, sermorelin acetate
Receptor Target
GHRH receptor on pituitary somatotrophs
Parent Hormone
Human growth hormone releasing hormone, 44 amino acids
Half-life
Short, on the order of minutes, owing to rapid DPP-4 cleavage at position 2
Appearance
White lyophilised powder
CAS number
86168-78-7

Evidence level: Phase I–II Clinical Trials (grade C)

Regulatory status: Previously FDA-approved (Geref, discontinued); now used off-label via compounding

Evidence grades describe the published literature on the compound, not a property of the material Volta supplies, and are not a statement that any use is approved. See how these grades are assigned.

Mechanism, in brief

Sermorelin is the amidated 1 to 29 fragment of human growth hormone releasing hormone. Native GHRH is 44 amino acids, but the first 29 carry essentially the full biological activity at the GHRH receptor, so the truncated peptide is a full agonist rather than a partial one. It acts at the GHRH receptor on the pituitary somatotroph, which is a different receptor from the ghrelin receptor targeted by secretagogues such as ipamorelin.

  1. Receptor binding. Full agonism at the GHRH receptor on pituitary somatotrophs. The 1 to 29 fragment retains the activity of the full 44 residue hormone.
  2. Cyclic AMP signalling. Gs-coupled signalling raises intracellular cyclic AMP, which triggers release of stored growth hormone and also stimulates its synthesis.
  3. Pulsatile secretion. Because it acts through the physiological pathway, secretion retains its episodic pattern rather than producing a sustained plateau.
  4. Feedback intact. The response remains subject to somatostatin tone and to negative feedback from circulating IGF-1, which limits the achievable elevation and distinguishes it from exogenous growth hormone.
  5. Diagnostic corollary. Because a response requires a functioning pituitary, absence of response localises the defect to the pituitary rather than the hypothalamus.

The full research write-up, including the findings behind each claim and the model each came from, is on the Sermorelin 10mg 10mg page.

Vial sizes available

Every size of Sermorelin Volta lists, in stock or not. Each is a separate catalogue page with its own batch number and specification table.

Purity and batch documentation

Volta's release specification is >99% (HPLC). That is a threshold we set. >99% is the specification every batch is released to. The figure on a certificate is what a laboratory measured for one lot.

No third-party certificate has been published for Sermorelinyet. The certificates Volta does publish, with the laboratory's own verification link on each, are in the certificate archive.

Research on Sermorelin

Handling and stability

Regulatory context

United States
Previously FDA-approved (Geref) for pediatric GH deficiency; voluntarily discontinued by manufacturer for commercial reasons. FDA confirmed in 2013 it was not withdrawn for safety. Available via compounding pharmacies. WADA-banned.
Canada
Not currently approved by Health Canada.
United Kingdom
Not MHRA-approved.

Primary sources

  1. Prakash A, Goa KL. Sermorelin: a review of its use in the diagnosis and treatment of children with idiopathic growth hormone deficiency. BioDrugs (1999). PMID 18031173
  2. Achermann JC, Hindmarsh PC, Brook CG. The relative roles of continuous growth hormone-releasing hormone (GHRH(1-29)NH2) and intermittent somatostatin withdrawal in growth hormone secretion. Clinical Endocrinology (Oxford) (1999). PMID 10594518
  3. Soule S, King JA, Millar RP. Incorporation of D-Ala2 in growth hormone-releasing hormone-(1-29)-NH2 increases the half-life and decreases metabolic clearance. Journal of Clinical Endocrinology and Metabolism (1994). PMID 7962295
  4. Ogilvy-Stuart AL, Stirling HF, Kelnar CJ, et al.. Treatment of radiation-induced growth hormone deficiency with growth hormone-releasing hormone. Clinical Endocrinology (Oxford) (1997). PMID 9231053
  5. The Medical Letter. Growth-hormone-releasing factor for growth hormone deficiency. The Medical Letter on Drugs and Therapeutics (1999). PMID 9924487
  6. Dominikowski A, Rękoś Z, et al.. The emerging landscape of performance-enhancing peptides modulating the GH-IGF1 axis. Frontiers in Endocrinology (2026). PMID 42395176

More growth hormone research peptides

Sermorelin sits in Volta's growth hormone research peptides catalogue, alongside the other compounds studied in this area. The whole range is on the full research catalogue, and the library of comparisons and guides is under peptide research.

Research use only. Every compound described on this page is supplied for in-vitro laboratory research. Nothing here is a recommendation for human or veterinary use, a dosing instruction, or a claim that any compound is a treatment for any condition. Published trial figures are reported as what an investigator administered in a named study, never as guidance. Read the full research disclaimer.

Cluster last reviewed: 2026-09-15.

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