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Comparison

GHRP-6 vs Sermorelin

Side-by-side of GHRP-6 and Sermorelin. Every row below is pulled from the compound schema and will update as our data grows. For deeper reads, follow through to each compound page.

Effects at a glance

GHRP-6

  • First-generation hexapeptide ghrelin-receptor agonist; foundational to the GHRP class
  • Strongest appetite stimulation of any synthetic GHRP at equivalent GH doses
  • Produces measurable cortisol and prolactin rise alongside the GH pulse
  • Anecdotal protocols use 100 to 200 mcg subcutaneously 2 to 3 times daily on an empty stomach
  • Largely superseded by ipamorelin (cleaner profile) and GHRP-2 (stronger pulse) for body-composition use
  • Banned by WADA under S2; detection methods validated in accredited labs

Sermorelin

  • Synthetic 29-amino-acid GHRH fragment; FDA approved 1997 for pediatric GH deficiency as Geref
  • Voluntarily discontinued by Serono in 2008 for commercial reasons; not safety-related
  • Compounded by 503A/503B pharmacies for off-label adult anti-aging and body-composition use
  • Produces physiologic pulsatile GH release; ~10 to 20 minute plasma half-life
  • Standard anti-aging clinic protocol: 200 to 500 mcg subcutaneously pre-bed, often with ipamorelin
  • Banned by WADA under S2 (peptide hormones, growth factors)

Side-by-side

Attribute GHRP-6 Sermorelin
Category peptide peptide
Also known as Growth Hormone Releasing Peptide 6, SKF-110679, Histidyl-D-Tryptophyl-Alanyl-Tryptophyl-D-Phenylalanyl-Lysinamide Sermorelin acetate, GRF 1-29, Geref, GHRH (1-29) NH2
Half-life (hr) 0.5 0.25
Typical dose (mg) 0.1 0.3
Dosing frequency 2-3x daily 1-2x daily
Routes subcutaneous, intravenous subcutaneous
Onset (hr) 0.25 0.25
Peak (hr) 0.5 0.5
Molecular weight 872.44 3357.88
Molecular formula C46H56N12O6 C149H246N44O42S
Mechanism Hexapeptide agonist of GHS-R1a (ghrelin receptor). Suppresses hypothalamic somatostatin and stimulates pituitary somatotrophs, with strong central NPY/AgRP appetite signaling and modest cortisol and prolactin release. Synthetic 29-amino-acid GHRH fragment that binds the GHRH receptor on pituitary somatotrophs to stimulate endogenous pulsatile GH synthesis and release while preserving the GH-IGF-1 negative feedback loop.
Legal status Not FDA approved; research-use-only grey market; banned by WADA FDA approved 1997 (Geref, pediatric GHD); voluntarily discontinued by Serono 2008; compounded by 503A/503B pharmacies for off-label adult use; banned by WADA
WADA status banned banned
DEA / Rx Not scheduled (research chemical) Rx only via compounding (no controlled-substance schedule)
Pregnancy Insufficient data; not recommended Category C (historical labeling); not recommended in pregnancy
CAS 87616-84-0 86168-78-7
PubChem CID 9919072 16129617
Wikidata Q5519921 Q416620

Safety profile

GHRP-6

Common side effects

  • intense hunger
  • water retention
  • vivid dreams
  • head pressure or flushing
  • tingling at injection site
  • transient lethargy

Contraindications

  • pregnancy
  • active malignancy
  • history of pituitary tumor
  • uncontrolled diabetes
  • prolactin sensitivity

Interactions

  • CJC-1295: synergistic GH release; commonly co-administered(minor)
  • sermorelin: additive GH release via parallel GHRH and ghrelin pathways(minor)
  • insulin: sustained GH can blunt insulin sensitivity over weeks(moderate)
  • corticosteroids: blunt GH response and amplify cortisol load(moderate)

Sermorelin

Common side effects

  • injection-site pain or irritation
  • transient flushing
  • headache
  • vivid dreams (pre-bed dosing)

Contraindications

  • pregnancy
  • active malignancy
  • history of pituitary tumor
  • diabetic retinopathy (theoretical)
  • untreated hypothyroidism

Interactions

  • ipamorelin: synergistic GH release via parallel GHRH and ghrelin pathways; standard anti-aging clinic pairing(minor)
  • CJC-1295: pharmacologically redundant (both GHRH-pathway); typically not stacked(minor)
  • insulin: sustained GH can blunt insulin sensitivity over weeks(moderate)
  • corticosteroids: blunt GH response; reduce expected efficacy(moderate)
  • levothyroxine (untreated hypothyroidism): untreated hypothyroidism blunts GH response; correct thyroid first(moderate)

Which Should You Take?

Sermorelin comes out ahead for most readers on the criteria we weight: 3 catalogued goals, FDA approved 1997 (Geref, pediatric GHD); voluntarily discontinued by Serono 2008; compounded by 503A/503B pharmacies for off-label adult use; banned by WADA, with a Tier-A outcome catalogued. GHRP-6 is the right call when one of the conditionals below applies.

  • If your priority is appetite regulation, pick GHRP-6.
  • If your priority is healthspan extension, pick Sermorelin.
  • If your priority is growth-hormone axis, pick Sermorelin.

Default choice: Sermorelin. Wider use case, a Tier-A evidence outcome catalogued, and broader goal coverage. Reach for GHRP-6 only if your priority sits squarely in the goals it owns above.

This verdict is generated from each compound's schema (goals, legal status, evidence outcomes, dosing route). It updates automatically as our compound data evolves; the deeper read sits on each individual compound page.

Common questions

What is the difference between GHRP-6 and Sermorelin?

GHRP-6 and Sermorelin differ in category (peptide vs peptide), mechanism, and typical dosing. See the side-by-side table for full details.

Which has a longer half-life, GHRP-6 or Sermorelin?

GHRP-6 half-life is 0.5 hours; Sermorelin half-life is 0.25 hours.

Can you stack GHRP-6 with Sermorelin?

Stack compatibility depends on mechanism overlap, legal status, and individual response. Check each compound page for specific interactions and contraindications before combining.

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