Growth Hormone

Ipamorelin

Selective GHS-R1a hexapeptide (Raun 1998, PMID 9849822). Quieter cortisol/prolactin/appetite than GHRP-6. Research chemical, not HGH, not an FDA anti-aging drug.

Not FDA-approved - research chemicalWADA (S2) - prohibited in sport at all times
Reviewed by CalcMyPeptide Editorial Team
Last updated: September 2026Evidence: Moderate3 peer-reviewed citations
Typical research dose
100-300 mcg/injection
Frequency
1-3× daily
Half-life
~2 hours
Common vials
2 mg / 5 mg
CAS
170851-70-4
Molecular weight
711.85 g/mol

Use-case scores

0–10 against the evidence we have, not a gym ranking. Hidden domains do not apply here.

  • Muscle / recomp4/10

    Raun 1998 is selectivity/GH-release pharmacology in animals and humans, not a hypertrophy RCT. Community ceiling after haircut: 4.

  • Recovery & sleep3.5/10

    Night pulses are GH physiology plus forums. Not a sleep trial.

Compound card

Sequence
Aib-His-D-2Nal-D-Phe-Lys-NH2
Class
Selective GHS-R1a hexapeptide (research; not a US GH drug)
Formula
C38H49N9O5
Status
Not FDA-approved · research use
Dose it
5 mg + 2.5 mL BAC water → 2 mg/mL · 100 mcg ≈ 5 units (U-100)
Open in calculator

How it works

Ipamorelin is a highly selective growth hormone secretagogue peptide (GHSP) that acts as a ghrelin receptor (GHS-R1a) agonist. Its defining characteristic is selectivity: unlike GHRP-6 and GHRP-2, Ipamorelin stimulates GH release without significantly elevating cortisol, prolactin, or appetite. That is the Raun 1998 story (Eur J Endocrinol, PMID 9849822), not a “cleanest anti-aging drug” label.

Ipamorelin stimulates the pituitary gland to release stored GH in a pulsatile pattern. It is often combined with CJC-1295 (no DAC) because GHRH and GHS-R are different receptors. Dual-receptor synergy is pharmacology. It is not a licensed GH product.

Source: PMID: 9849822

Goal context

Clean GHRP in a GHRH stack

Ipamorelin is the selective GHS-R1a pick clinics pair with Mod GRF / CJC no-DAC. Cortisol/prolactin sparing vs GHRP-6 is the Raun 1998 story, not a cleanliness ranking from a head-to-head recomp RCT.

Not somatropin

A research hexapeptide pulse is not prescription GH. Dual-receptor synergy with a GHRH analog is pharmacology, not a licensed product.

Background & History

Ipamorelin is a GHS-R1a hexapeptide from Novo screening (Raun 1998). Selectivity vs first-generation GHRPs is the pharmacology story. It is not FDA-approved HGH and not a sleep drug.

Research Use Cases

  • ✓Selective GHRP identity vs GHRP-2/6 and hexarelin
  • ✓Why it is the default stack partner for Mod GRF
  • ✓Not a somatopause or body-recomp NDA

Dosing

PhaseDoseFrequencyNotes
Standard Protocol100 - 200 mcg1-3× dailyInject fasted. 1hr no food before, 30min after. Most popular: before bed + upon waking.
Stacked with CJC-1295100 mcg Ipamorelin + 100 mcg CJC-1295 No DAC1-3× dailyIndustry gold-standard GH stack. Synergistic amplitude and initiation.

Administration

Route / form
Subcutaneous injection
Timing
Must be injected fasted. Most common: before sleep (aligns with nighttime GH surge) and/or upon waking.
Empty stomach?
Yes - Empty stomach (typical for this injectable class).

Timeline

Week 1-2
Improved sleep depth and quality. Faster recovery between training sessions.
Month 1-2
Gradual body composition improvements: increased lean mass, mild fat reduction.
Month 3+
Compounding IGF-1 elevation and sustained body recomposition.

Who it is for

GH Optimization (Clean)

High

Selective GH release without cortisol, prolactin, or appetite spikes - the cleanest GHRP.

Anti-Aging / Longevity

Moderate

Long-term GH/IGF-1 support with minimal systemic side effects.

Reconstitution

VialWaterConcentrationExample dose
5 mg lyophilized2.5 mL BAC2 mg/mL200 mcg = 0.10 mL = 10 units on a U-100.

Change vial size or water volume? Open the reconstitution calculator.

Safety & Considerations

Research peptide with a favorable safety profile in studies. May cause transient headache or lightheadedness. Minimal effect on cortisol, prolactin, or appetite (unlike GHRP-6). Inject on an empty stomach for optimal GH pulse.

Regulatory & Legal Status

FDA Status (US)
Research Only
WADA Status (2026)
Prohibited (S2)

Competitive athletes subject to anti-doping controls should not use Ipamorelin.

Classification

Compounded Drug (Rx)

US Compounding: Available via licensed pharmacy Rx

⚠️ This information is for educational purposes only and may not reflect the most current regulatory updates. Always verify with official FDA, WADA, and jurisdiction-specific sources before use.

Limits of current evidence

  • Selectivity vs GHRP-6 is the paper. Body-recomp timelines are community.
  • Do not print a 2–5× GH multiplier for ipa + Mod GRF as if it were a trial endpoint.
  • Research chemical in the US wellness market. Not Geref. Not Egrifta.

Human evidence

Moderate · selectivity pharmacology (not a hypertrophy RCT)

  • Raun 1998 (PMID 9849822) is selectivity/GH-release pharmacology — not a hypertrophy or anti-aging RCT.
  • Research chemical in the US wellness market. Not Geref. Not Egrifta.

Verdict

Ipamorelin is the GHRP people mean when they say “clean.” Raun 1998 (PMID 9849822) is why cortisol/prolactin/appetite are quieter than GHRP-6. It is not HGH, not FDA-approved for anti-aging, and a stack slogan is not a label.

Interactions & Contraindications

Food/insulin can blunt the pulse. Do not add somatropin because IGF-1 is already high. Somatostatin analogs antagonize GH release.

Synergies & Common Stacks

Classic GHRH+GHRP mix. Dual-receptor physiology is real. “2–5× more GH than either alone” is not a trial endpoint at 100/100 mcg.

Weekly albumin-binder plus a daily pulse peptide is convenience folklore. Confirm you are not double-counting Teichman.

Ipamorelin vs. GHRP-6

Canonical comparison: Ipamorelin vs GHRP-6

AttributeIpamorelinGHRP-6
SelectivityHigh - GH only, no cortisol/prolactinLow - GH + cortisol + prolactin + ghrelin
Appetite EffectMinimal stimulationStrong appetite stimulation
GH OutputModerate, clean, dose-dependentStrong, non-selective pulse
Best ForAnti-aging, long-term clean protocolMuscle building, caloric surplus phase
Side EffectsMinimal (transient water retention)More (hunger, cortisol elevation)

Verdict: Ipamorelin is cleaner and better tolerated for long-term use. GHRP-6 is better for appetite-driven muscle-building phases where hunger stimulation is a feature, not a bug.

Ipamorelin vs. CJC-1295 (No DAC)

Canonical comparison: Ipamorelin vs CJC-1295 (No DAC)

AttributeIpamorelinCJC-1295 (No DAC)
ClassGHRP (ghrelin mimetic)GHRH analog (growth hormone-releasing hormone)
MechanismTriggers GH pulse via pituitaryAmplifies GH pulse amplitude
Stacked TogetherIndustry gold-standard combinationIndustry gold-standard combination
Half-Life~2 hours~30 minutes
Solo EffectivenessModerate GH pulse aloneModerate amplitude increase alone

Verdict: Ipamorelin + CJC-1295 (No DAC) is the most widely used GH optimization stack in current protocols. They are complementary, not competing: GHRP initiates the pulse, GHRH amplifies it.

Frequently Asked Questions

What makes Ipamorelin better than GHRP-6?▼
Ipamorelin is more selective - it stimulates GH release without significantly raising cortisol, prolactin, or appetite. GHRP-6 strongly stimulates hunger (via ghrelin pathway), which many users find undesirable.
What is the standard Ipamorelin dose?▼
100-300 mcg per injection, 1-3 times daily on an empty stomach. Most commonly used at 100-200 mcg combined with 100 mcg CJC-1295 (no DAC).
How long does it take to see results from Ipamorelin?▼
Sleep quality improvements are often noticed within the first 1-2 weeks. Body composition changes typically require 8-12 weeks of consistent dosing.

References

  1. Raun et al. “"Ipamorelin, the first selective growth hormone secretagogue".” European Journal of Endocrinology (1998). PMID: 9849822
  2. Raun K, et al. “Ipamorelin, the first selective growth hormone secretagogue.” Eur J Endocrinol (1998). PMID: 9703375
  3. Gobburu JV, et al. “Safety and tolerability of ipamorelin in healthy subjects.” Growth Horm IGF Res (2009). PMID: 19411194

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