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Sermorelin 2mg

Price range: $2,500.00 through $10,000.00

Features of wholesale peptide






Sermorelin Wholesale | GHRH Analog Bulk Supply | 2mg Research Peptide 2026



Compounding Pharmacy Staple · Anti-Aging Clinic Standard · FDA-Approved History

Sermorelin Wholesale
GHRH Analog Bulk Supply

The original GHRH analog — FDA-approved history, three decades of published research, and the most trusted GH secretagogue in compounding pharmacy practice. Sermorelin (GHRH 1-29 NH₂) stimulates pituitary somatotrophs to produce endogenous GH via the GHRH receptor — preserving the hypothalamic-pituitary axis and natural pulsatile secretion patterns that exogenous GH replacement cannot replicate.

Anti-Aging · GH Axis · Longevity
FDA-Approved History (Geref®)
≥98% HPLC Purity
Full COA Included
2mg Vials
Compounding Pharmacy Staple
MOQ: 10 Vials
≥98%
HPLC Purity
29
Amino Acids
48h
Fulfillment

Product Overview

What Is Sermorelin? The Original GHRH Analog Explained

Sermorelin (GHRH 1-29 NH₂) is a synthetic peptide corresponding to the first 29 amino acids of endogenous human growth hormone-releasing hormone (GHRH) — the biologically active N-terminal fragment responsible for pituitary GH stimulation. Unlike exogenous human growth hormone (HGH) which bypasses the hypothalamic-pituitary axis entirely, sermorelin acts upstream at the pituitary GHRH receptor (GHRHR), stimulating somatotroph cells to produce and release endogenous GH through the body’s own regulated secretion system.

Sermorelin was FDA-approved in 1997 as Geref® (Serono Laboratories) — making it the first synthetic GHRH analog to achieve regulatory approval for GH deficiency diagnosis and treatment in children. Geref® was voluntarily withdrawn from the US commercial market in 2008 for business reasons, not safety concerns — and sermorelin continued its clinical life through compounding pharmacy channels, where it became the foundational GH secretagogue for anti-aging and longevity medicine practice through the 2010s and into the current decade.

For wholesale buyers, sermorelin represents the most clinically validated entry point in the GHRH analog category. Its three-decade published research base, FDA approval history, and established compounding pharmacy presence give it institutional credibility that newer GHRH analogs like CJC-1295 cannot match. Competitor listings don’t carry it — making sermorelin a direct market opportunity with consistent demand from compounding pharmacies and longevity clinics.

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The Original GHRH Analog

Sermorelin is GHRH(1-29)NH₂ — the N-terminal 29-amino-acid fragment of native GHRH. It was characterized in the 1980s by researchers studying GHRH structure-activity relationships, FDA-approved in 1997, and has accumulated more published human clinical data than any other GHRH analog in the wholesale peptide catalog.

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Endogenous GH Stimulation

Sermorelin activates GHRH receptors on pituitary somatotrophs, increasing intracellular cAMP via Gs protein coupling, driving GH gene transcription and pulsatile secretion. Because it stimulates the body’s own GH production pathway — rather than replacing GH exogenously — it preserves the hypothalamic-pituitary axis, somatostatin-mediated feedback, and natural GH pulse patterns.

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FDA-Approved Clinical History

Geref® (sermorelin acetate injection) was FDA-approved in 1997 for two indications: GH deficiency diagnosis (GH stimulation test) and treatment of idiopathic GH deficiency in children. This regulatory history provides sermorelin with pharmacokinetic, safety, and efficacy data from FDA clinical trials — a published clinical foundation unavailable for any other GHRH analog in wholesale research supply.

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Compounding Pharmacy Staple

Since Geref® market withdrawal in 2008, sermorelin has been continuously supplied through 503A compounding pharmacies for GH optimization protocols. Its 20+ year compounding history, well-established dosing conventions, and physician familiarity make it the standard entry-level GHRH analog for longevity and anti-aging medicine practices starting GH secretagogue programs.

Mechanism of Action

How Sermorelin Works — The GHRH Receptor Pathway

Sermorelin’s mechanism is clean and well-characterized from three decades of published research. It acts exclusively at the pituitary GHRH receptor — a Gs protein-coupled receptor on somatotroph cells — with no direct activity at any other receptor system. This specificity makes sermorelin one of the most precisely targeted peptides in the GH secretagogue wholesale catalog.

Sermorelin → GH Secretion Pathway

The complete signal cascade from sermorelin administration to pulsatile GH release:

SermorelinSubcutaneous / IV administration
GHRHR BindingPituitary somatotrophs
Gs/cAMP ↑Adenylyl cyclase activation
PKA → CREBGH gene transcription
GH Pulse ReleasePulsatile · somatostatin-regulated

A critical research advantage: sermorelin preserves somatostatin-mediated negative feedback. When GH levels rise sufficiently, somatostatin from the hypothalamus inhibits further GH secretion — an autoregulatory mechanism that functions normally with sermorelin but is bypassed with exogenous HGH administration. This preservation of physiological feedback is a central topic in GH axis research and a key reason sermorelin is preferred over HGH in protocols studying natural GH axis dynamics.

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Gs/cAMP/PKA Cascade

GHRHR is a Gs-coupled GPCR. Sermorelin binding activates adenylyl cyclase via Gs, increasing intracellular cAMP. Elevated cAMP activates PKA, which phosphorylates CREB transcription factor — driving GH gene transcription and GH synthesis in somatotroph cells.

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Preserved Pulsatile Profile

Unlike continuous HGH replacement, sermorelin-stimulated GH follows the body’s natural pulsatile secretion pattern — highest at night during deep sleep, modulated by somatostatin, IGF-1 feedback, and nutritional status. Pulsatile GH research requires this preserved pattern; exogenous HGH cannot replicate it.

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Negative Feedback Intact

Somatostatin (SRIF), released from the hypothalamus in response to rising IGF-1 and GH, inhibits GHRHR signaling — keeping GH in physiological range. This autoregulation is absent with exogenous HGH and is a protective pharmacological feature studied extensively in anti-aging research contexts.

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Short Half-Life — Natural Kinetics

Sermorelin has a half-life of approximately 10–15 minutes — close to endogenous GHRH. This brief, pulsatile stimulation profile produces discrete GH pulses that best approximate natural hypothalamic-pituitary signaling, making it the preferred compound for research studying native GH axis physiology.

Product Comparison

Sermorelin vs CJC-1295 vs Tesamorelin — GHRH Analog Comparison

Sermorelin, CJC-1295 (no DAC), and tesamorelin are the three primary GHRH analogs in wholesale research supply. Understanding their structural and pharmacokinetic differences is critical for research protocol selection and wholesale catalog curation.

Property Sermorelin CJC-1295 No DAC Tesamorelin
Amino Acids 29 (native GHRH sequence) 29 (4 substitutions) 44 (full GHRH + trans-3-hexenoic acid)
Molecular Weight 3,357.93 Da 3,367.97 Da 5,135.74 Da
Half-Life ~10–15 min ~30 min ~25–38 min
Relative GHRHR Potency Baseline (1×) ~49× vs native GHRH Higher than sermorelin
Amino Acid Substitutions None — native sequence 4 substitutions (D-Ala², Ala⁸, Ala⁹, Ala¹⁵) Trans-3-hexenoic acid conjugated
FDA Approval History Yes — Geref® (1997, withdrawn 2008) No Yes — Egrifta® (2010, HIV lipodystrophy)
Compounding Pharmacy Use 20+ year history Common (blend protocols) Less common
Best Research Application Native GHRH axis research, compounding pharmacy programs Combination GHRH+GHRP protocols, enhanced potency Visceral fat/metabolic GHRH research
Ipamorelin Stack ✓ Compatible ✓ Standard combination Less common

Sermorelin’s distinct position: the only GHRH analog in wholesale supply with the native 29-amino-acid sequence (no structural modifications), FDA-approved clinical history, and 20+ years of compounding pharmacy use. For research programs requiring a GHRH analog closest to endogenous GHRH — or for compounding pharmacies with established sermorelin protocols — it is the correct choice.

Technical Specifications

Sermorelin Wholesale — Full Specifications

Chemical & Molecular Data

Full Name Sermorelin (GHRH 1-29 NH₂)
Also Known As GRF(1-29)NH₂, Sermorelin acetate, Geref® (withdrawn)
Amino Acids 29 (native GHRH N-terminal sequence)
Molecular Weight 3,357.93 Da
CAS Number 86168-78-7
Target Receptor GHRH Receptor (GHRHR) — Gs-coupled
Half-life ~10–15 minutes
Physical Form Lyophilized white powder

Quality & Purity Standards

HPLC Purity ≥98% (batch tested)
Identity Mass spectrometry (MW 3,357.93 Da)
Endotoxin <1 EU/mg (LAL method)
Sterility Sterile-filtered, aseptic fill
Water Content <5% (Karl Fischer)
Residual Solvents ICH Q3C compliant
Storage (lyophilized) -20°C · 24+ months
Post-reconstitution 4°C · use within 28 days

Wholesale Pricing

Sermorelin Wholesale Price — Volume Tiers 2026

Sermorelin is the most affordable GHRH analog per vial in the wholesale catalog — making it accessible for high-volume compounding and research programs while maintaining research-grade quality standards.

Quantity Total Price Per Vial Per mg Availability
Sermorelin 2mg × 1 $18 $18 $9.00 / mg ✓ In Stock
Sermorelin 2mg × 10CLINIC PACK $160 $16 $8.00 / mg ✓ In Stock
Sermorelin 2mg × 25 $375 $15 $7.50 / mg ✓ In Stock
Sermorelin 2mg × 50 $700 $14 $7.00 / mg ✓ In Stock
Sermorelin 2mg × 100+ Contact Custom Custom rate ✓ In Stock
Also Available: Sermorelin 5mg and 10mg vials available for high-volume compounding programs requiring larger per-vial dose. CJC-1295 no DAC + Ipamorelin blend also available for programs transitioning from sermorelin to enhanced-potency GHRH analog stacks. Contact B2B desk for multi-compound institutional pricing packages.

Research Context

Sermorelin in Published Research — Three Decades of Evidence

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FDA Clinical Trials — Geref® Approval Data (1997)

Sermorelin’s FDA approval as Geref® in 1997 required submission of pivotal clinical trial data demonstrating efficacy for GH stimulation testing and treatment of idiopathic GH deficiency in children. Published pharmacokinetic studies from the Geref® program characterized sermorelin’s half-life (~10–15 minutes), GH pulse response, IGF-1 normalization data, and safety profile across pediatric populations — the most extensively characterized clinical dataset of any GHRH analog in wholesale supply.

Geref® FDA approval documents; multiple clinical trial publications 1993–2003

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Adult GH Deficiency & Anti-Aging Research

Walker RF (2006, Clinical Interventions in Aging) published a landmark review of sermorelin in adult GH deficiency, examining its role as an alternative to exogenous HGH therapy. The paper established the rationale for sermorelin in adult longevity medicine — specifically the preservation of HPG axis integrity, somatostatin feedback, and pulsatile secretion patterns — that became the foundation for compounding pharmacy sermorelin programs. This paper is widely cited in anti-aging and longevity medicine literature.

Walker RF, Clinical Interventions in Aging, 2006

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GHRH Receptor Biology & Pituitary Research

Sermorelin’s role as a selective GHRHR agonist has made it a standard pharmacological tool in pituitary biology research. Published studies have used sermorelin to characterize GHRHR expression patterns, receptor desensitization dynamics, Gs/cAMP/PKA signaling in somatotrophs, and the pituitary response to GHRH across age groups. Its native sequence (no amino acid substitutions) makes it the preferred compound for research requiring the closest approximation to endogenous GHRH signaling.

Extensive publication record in Endocrinology, Journal of Clinical Endocrinology & Metabolism, Neuroendocrinology

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GH Axis, Sleep, & Cognitive Research

Published research has studied sermorelin’s effects on sleep architecture (GH secretion is highest during slow-wave sleep; sermorelin enhances this nocturnal GH pulse in published studies), cognitive function in GH-deficient populations, body composition parameters, and bone mineral density. These downstream GH axis effects — all dependent on preserved pulsatile secretion that sermorelin maintains — are active research areas in longevity and aging medicine programs.

Multiple publications in Growth Hormone & IGF Research, Journal of Clinical Endocrinology & Metabolism, 1990s–2020s

Quality & Documentation

Sermorelin Wholesale Quality Standards

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Full COA Per Lot

Every batch COA available pre-purchase. HPLC purity, mass spec identity (3,357.93 Da). Lot numbers match vials.

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HPLC + Mass Spec

Purity ≥98% by HPLC. Identity confirmed by mass spectrometry every batch.

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Endotoxin + Sterility

LAL endotoxin <1 EU/mg. Sterile-filtered, aseptic fill confirmed per batch.

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Sequence Integrity

Native 29-AA sequence verified. No unintended substitutions — critical for GHRH native-sequence research.

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Cold-Chain Shipping

Ships cold-chain. -20°C stable 24+ months lyophilized. Once reconstituted: 28 days at 4°C.

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48h Fulfillment

In-stock orders ship within 48 business hours with cold-chain manifest and tracking.

Buyer Qualification

Who Buys Sermorelin Wholesale

Sermorelin’s compounding pharmacy heritage and FDA-approved history give it the broadest institutional buyer base of any GHRH analog. Not available to the general public.

Compounding Pharmacies

503A pharmacies with established sermorelin compounding programs represent the highest-volume wholesale buyer. 20+ years of compounding use means established protocols, trained staff, and consistent institutional demand.

Longevity & Anti-Aging Clinics

The core prescriber base for sermorelin protocols. Physician-supervised programs using sermorelin as the entry-level GHRH analog for GH optimization research.

Endocrinology Research Programs

Academic endocrinology labs and CROs using sermorelin as a pharmacological GHRH tool in pituitary biology, GH axis, and somatotroph research.

Men’s & Women’s Health Practices

Hormone optimization practices incorporating sermorelin into comprehensive GH, testosterone, and metabolic health research programs.

Regenerative Medicine Clinics

Regenerative practices using sermorelin in tissue repair and recovery research contexts, often alongside BPC-157, TB-500, or NAD+ protocols.

Pediatric & GH Deficiency Research

Research institutions studying GH deficiency mechanisms or pediatric GH axis physiology — sermorelin’s FDA-approved pediatric indication provides the most relevant published clinical reference data.

FAQ

Sermorelin Wholesale — Frequently Asked Questions

Sermorelin (GHRH 1-29 NH₂) is a synthetic 29-amino-acid peptide identical to the N-terminal biologically active fragment of endogenous human GHRH. It binds GHRH receptors (GHRHR) on pituitary somatotroph cells, activating a Gs/cAMP/PKA cascade that drives GH gene transcription and pulsatile GH secretion. Unlike exogenous HGH which replaces GH and suppresses the HPG axis, sermorelin stimulates the body’s own GH production pathway — preserving somatostatin-mediated negative feedback and natural pulsatile GH secretion patterns.

Yes. Sermorelin was FDA-approved in 1997 as Geref® (Serono Laboratories) for two indications: (1) diagnostic GH stimulation testing in patients with suspected GH deficiency, and (2) treatment of idiopathic growth hormone deficiency in children with growth failure. Geref® was voluntarily withdrawn from the US commercial market in 2008 for commercial/business reasons — not for safety concerns, adverse event findings, or efficacy issues. The compound continued to be supplied through 503A compounding pharmacies after commercial withdrawal and remains in active compounding use today.

Both are 29-amino-acid GHRH receptor agonists, but they differ in three key ways. Structure: Sermorelin is the native GHRH(1-29) sequence with no modifications. CJC-1295 no DAC (Modified GRF 1-29) contains four amino acid substitutions (D-Ala², Ala⁸, Ala⁹, Ala¹⁵) that enhance proteolytic resistance. Potency: CJC-1295 binds GHRHR with approximately 49× greater potency than native GHRH; sermorelin binds at native GHRH potency. Half-life: Sermorelin ~10–15 minutes; CJC-1295 no DAC ~30 minutes. For protocols requiring the closest approximation to native GHRH signaling, sermorelin is the correct choice. For higher potency and longer-acting GH stimulation, CJC-1295 is preferred.

Yes. Sermorelin + ipamorelin is a well-established combination in compounding pharmacy practice, following the same dual-pathway rationale as CJC-1295 + ipamorelin: sermorelin activates GHRH receptors (cAMP/PKA pathway, amplitude), ipamorelin activates GHS-R1a ghrelin receptors (Ca²⁺/PKC pathway, frequency). The combination produces synergistic GH stimulation. The sermorelin + ipamorelin stack predates the CJC-1295 combination chronologically — it was the original GHRH + GHRP combination used in compounding pharmacy GH protocols before CJC-1295 became widely available.

Minimum order is 10 vials. Volume pricing at 10, 25, 50, and 100+ unit thresholds. Compounding pharmacies and high-volume longevity clinics (50+ vials/month) qualify for custom institutional pricing with NET 30 terms. Sermorelin 5mg and 10mg vials also available for programs requiring larger per-vial doses — contact our B2B desk for multi-size institutional pricing packages.

Sermorelin is the unmodified native GHRH(1-29) sequence — it is susceptible to rapid cleavage by dipeptidyl peptidase-4 (DPP-4) and other endogenous proteases at the same sites as endogenous GHRH, resulting in a half-life of approximately 10–15 minutes. CJC-1295 was engineered with four amino acid substitutions specifically to protect against DPP-4 and other protease cleavage sites, extending its half-life to ~30 minutes. This is not a disadvantage for all research contexts — sermorelin’s shorter, more pulsatile profile is preferred for protocols studying native GH axis kinetics and natural secretion patterns.

Research Use Only: Sermorelin and all products on this page are sold strictly for in vitro research, laboratory, and licensed compounding use only. Not intended for unsupervised human therapeutic use. Sermorelin was previously FDA-approved as Geref® (withdrawn 2008 for commercial reasons, not safety). Research-grade sermorelin wholesale is not the approved drug product. No claims are made regarding therapeutic efficacy or safety outside of licensed research or compounding contexts. Buyers are solely responsible for compliance with all applicable federal, state, and local laws. By purchasing, you confirm you are a licensed researcher, compounding pharmacist, or qualified institutional buyer acting within the scope of a legitimate program.



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