
2X Blend CJC-1295 Without DAC / Ipamorelin
The 2X Blend combines CJC-1295 Without DAC and Ipamorelin — the standard GHRH+GHRP research combination producing synergistic, selective GH pulse amplification through two independent receptor systems.
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Sermorelin is a 29-amino-acid synthetic GHRH(1-29) analog — the first FDA-approved GHRH peptide (Geref), with the longest published research history of any synthetic GHRH compound.
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In your order
Lyophilized vial
Sterile-filtered, freeze-dried peptide in glass vial, sealed under inert gas.
Lot ID on every vial
Printed lot ID ties this exact vial to its analytical record.
COA on request
Independent third-party HPLC certificate, matched to your lot, sent on request.
Carrier-tracked shipping
Shipped from a US facility with full carrier tracking and protective packaging.
The Peptific standard
Peptide quality is invisible until it isn’t. Lot identity, purity, fill integrity, and chain of custody are the difference between usable research material and wasted budget.
Third-party HPLC tested
Every lot is tested for identity and purity by an independent analytical lab. Certificate of Analysis available on request, tied to the exact lot you receive.
Lyophilized and lot-tracked
Sterile-filtered, freeze-dried, sealed under inert gas. Each vial carries its own lot ID — full chain of custody from fill to delivery.
US-based fulfillment
Orders ship from a temperature-controlled US facility with carrier tracking. No drop-shipping, no opaque overseas relay.
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A real person responds to research questions, lot questions, and order questions — usually same business day. No bot triage.
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How it works
Sermorelin binds GHRH receptors on pituitary somatotropes via the active N-terminal sequence of native GHRH, stimulating pulsatile GH release through cAMP signaling. The endogenous feedback axis (somatostatin, IGF-1) remains intact, producing physiologically patterned GH pulses. Half-life ~10–20 minutes in vivo; short active window defines its research utility in acute GH pulse studies.
Compound profile
Product definition
Sermorelin is a 29-amino-acid synthetic GHRH(1-29) analog — the first FDA-approved GHRH peptide (Geref), with the longest published research history of any synthetic GHRH compound.
Sermorelin (also designated GHRH(1-29)NH2) is the C-terminally amidated 29-amino-acid N-terminal fragment of the 44-amino-acid endogenous GHRH. Studies dating to the 1980s established that GHRH(1-29) retains full receptor binding and GH-stimulating potency relative to the full-length peptide — the C-terminal residues beyond position 29 contribute little to biological activity. The FDA approved sermorelin (as Geref, Serono) for GH deficiency in pediatric patients, establishing the first regulatory approval for any synthetic GHRH compound. This regulatory dataset provides human pharmacokinetic characterization (dose-response, GH AUC, IGF-1 normalization) that constitutes the foundational GHRH analog research literature. Sermorelin's short half-life distinguishes it from tesamorelin (trans-3-hexenoic acid N-terminal modification, ~26 minutes) and CJC-1295 variants (30 minutes to 6–8 days), positioning sermorelin as the first-generation reference compound for short-duration GHRH receptor activation protocols.
Research audience
Sermorelin is used by researchers studying GHRH receptor pharmacology, GH pulse physiology, pituitary somatotrope function, GH deficiency models, and GH axis response to intervention. It is particularly relevant for labs requiring a historically grounded reference GHRH compound with published human pharmacokinetic data.
Research context
Sermorelin's research history predates the modern synthetic peptide research supply market. Published human studies from the 1980s and 1990s characterized its dose-response relationship for GH stimulation, its utility in GH deficiency testing (GH stimulation test), and its effects on body composition in GH-deficient children. This long publication record makes sermorelin uniquely interpretable — there is decades of experimental context for its pharmacological effects. In animal model research, sermorelin has been studied for age-related GH secretion decline (somatopause), GH axis response to chronic administration, and pituitary somatotrope sensitivity. The preserved feedback axis under sermorelin administration (versus direct GH supplementation) has made it a useful model for studying the regulated GH secretion system rather than simply supplying GH exogenously. For comparative pharmacology research, sermorelin serves as the baseline against which newer GHRH analogs are evaluated. The improvements from sermorelin to tesamorelin (DPP-IV resistance), CJC-1295 Without DAC (four protective substitutions), and CJC-1295 With DAC (albumin binding, 6–8 day half-life) each represent incremental pharmacokinetic advances measured against the sermorelin baseline.
Common questions
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2X Blend CJC-1295 Without DAC / Ipamorelin
The 2X Blend combines CJC-1295 Without DAC and Ipamorelin — the standard GHRH+GHRP research combination producing synergistic, selective GH pulse amplification through two independent receptor systems.

CJC-1295 Without DAC
CJC-1295 Without DAC (MOD GRF 1-29) is a tetrasubstituted GHRH(1-29) analog with ~30-minute half-life — the preferred short-acting GHRH analog for pulsatile GH research protocols, commonly paired with ipamorelin.

CJC-1295 With DAC
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CJC-1295 With DAC is a long-acting GHRH analog with albumin-binding modification that sustains elevated GH and IGF-1 for 6–8 days per administration in preclinical and early clinical research.

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GHRP-6 is a hexapeptide GHS-R1a agonist and the founding GHRP compound — studied in preclinical models for GH release, significant appetite stimulation, and cortisol co-stimulation via ghrelin receptor activation.

Ipamorelin
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Ipamorelin is a selective pentapeptide GHRP studied in preclinical models for GH release without cortisol or prolactin elevation — the most selective GHRP in its class.

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IGF-DES

Tesamorelin
$29.00
Tesamorelin is a 44-amino-acid GHRH analog with N-terminal trans-3-hexenoic acid modification — the only FDA-approved GHRH peptide, validated in Phase III trials for visceral adiposity reduction.

MOD GRF 1-29
MOD GRF 1-29 (CJC-1295 Without DAC) is a tetrasubstituted GHRH(1-29) analog with ~30-minute half-life — the most commonly used short-acting GHRH compound for pulsatile GH secretion research.

GHRP-2
GHRP-2 (Pralmorelin) is a synthetic hexapeptide GHS-R1a agonist approved in Japan for GH stimulation testing — a potent non-selective GHRP that stimulates GH alongside cortisol and prolactin.
Research Use Only
Sold for laboratory and research purposes only. Not approved for, nor intended for, human or veterinary consumption, diagnostic use, or therapeutic application. These products have not been evaluated by the Food and Drug Administration. Keep out of reach of children. For use by qualified researchers only.
Nothing on this page constitutes medical advice, a treatment recommendation, or a clinical protocol. Consult a qualified healthcare provider before making any health or treatment decisions.
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