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GHRP2-5mg

Specification Detail
Category Growth Hormone Secretagogue (GHS)
Product Name GHRP-2 (Pralmorelin)
Quantity 5mg (Total Active API)
Formulation Sterile Lyophilised Solution in Bacteriostatic Water
Delivery Method 3ml Precision Reconstituted Pen
CAS Number 158861-67-7
Molecular Formula $C_{45}H_{55}N_{9}O_{6}$
Molecular Weight $\approx 817.9 \text{ g/mol}$
Purity >98% (HPLC Analysis)

£109.00

Abstract The GHRP-2 5mg peptide pen contains a high-purity solution of Pralmorelin (Growth Hormone Releasing Peptide-2), a synthetic hexapeptide of the Growth Hormone Secretagogue (GHS) class. Structurally composed of D-Ala-D-2-Nal-Ala-Trp-D-Phe-Lys-, GHRP-2 is recognised as one of the most potent stimulators of growth hormone release currently available for research. Unlike the first-generation GHRP-6, GHRP-2 exhibits a refined pharmacological profile: it retains high affinity for the GHS-R1a receptor to drive intense somatotropic activity but triggers significantly less orexigenic (appetite) stimulation. This 5mg formulation is the standard reagent for investigating acute GH pulsatility and evaluating the “ceiling effect” of pituitary output in catabolic models.

Mechanism and Research Interest

Primary Biological Pathway: Intense GH Secretion The defining characteristic of GHRP-2 is its raw potency. It acts as a full agonist at the GHS-R1a receptor on pituitary somatotrophs. Upon binding, it triggers a massive influx of intracellular calcium via the Phospholipase C (PLC) pathway, causing the immediate exocytosis of growth hormone vesicles. Research utilising the 5mg pen focuses on quantifying this secretory spike, which is often 10-15 times higher than basal levels. It is frequently used to test the functional reserve of the pituitary gland in models of secondary growth hormone deficiency.

Secondary Research Finding: Reduced Orexigenic Effect While GHRP-6 is famous for inducing extreme hunger via hypothalamic NPY neurons, GHRP-2 induces this effect to a much lesser degree. This makes GHRP-2 the preferred reagent for metabolic studies where GH upregulation is desired without the confounding variable of hyperphagia (overeating). Researchers use the 5mg pen to isolate the lipolytic (fat-burning) effects of Growth Hormone from the caloric intake usually associated with Ghrelin mimetics.

Tertiary Research Finding: ACTH and Prolactin Modulation Unlike the “selective” Ipamorelin, GHRP-2 is slightly “promiscuous.” At saturation doses, it can stimulate a transient release of ACTH (cortisol) and Prolactin. While often considered a side effect, this property is valuable for neuro-endocrine stress testing. The 5mg pen allows researchers to dose-range the “specificity window”—identifying the precise concentration where GH release is maximised while corticotropic stimulation remains minimal.

Long-term Genomic and Safety Observations A critical aspect of GHRP-2 research is Tachyphylaxis (desensitisation). Continuous exposure can downregulate the GHS-R1a receptor. Genomic studies utilising the 5mg pen investigate dosing frequencies (e.g., TID vs. QID) to establish protocols that maintain receptor density (Ghsr mRNA expression) over longitudinal studies, preventing the “burnout” of the somatotropic axis.

Product Specifications

  • Purity: Validated at >98+% via High-Performance Liquid Chromatography (HPLC). We strictly control the synthesis to ensure the D-isomer amino acids are correctly incorporated, which protects the peptide from rapid degradation by blood serum enzymes.

  • Appearance: The 3ml pen contains a clear, colourless, sterile liquid.

  • Precision: The pen delivery system ensures accurate volumetric dosing. This is essential for “Stacking” protocols (e.g., combining with Mod GRF 1-29), where the molar ratio of the two peptides determines the synergistic amplitude of the GH pulse.

  • Storage: The product must be stored at to .

Storage and Shipping Guidelines

Refrigeration and Shelf Life The GHRP-2 5mg Pen contains a stable hexapeptide but requires refrigeration ( to ). The shelf life is 12 months in the sealed state. Once the pen is accessed, the bacteriostatic environment preserves the solution for 28 days. Researchers should be aware that while GHRP-2 is chemically robust, leaving it at room temperature can accelerate the hydrolysis of the C-terminal amide, reducing its receptor affinity.

Shipping Stability We utilise medical-grade thermal packaging. The peptide is stable for up to 72 hours at ambient UK temperatures. However, to ensure the highest fidelity for receptor interaction studies, we recommend selecting the fastest available shipping option.

Freezing Warning Do not freeze. Freezing can cause the peptide to precipitate out of the solution. Upon thawing, re-solubilisation may be incomplete, leading to non-homogenous dosing. This variability can drastically skew quantitative data regarding GH serum levels. A frozen pen should be discarded.

Why Choose the Peptide Pro 3ml Pen Format?

The GHRP-2 5mg Pen is the definitive tool for Potent Somatotropic Research. When maximal GH release is the goal, GHRP-2 is the standard. However, because it has a narrow therapeutic window regarding cortisol release, precise dosing is non-negotiable.

Our precision pen provides a sterile, concentration-verified solution that allows for exact micro-dosing. This ensures researchers can hit the “sweet spot” of maximal anabolic signaling without triggering the catabolic stress response associated with accidental overdosing.

For researchers scrutinising the specificity of the secretagogue, we recommend examining:

  • Ipamorelin 10mg:  (For zero-cortisol/prolactin research).

  • GHRP-6 10mg: (For research specifically investigating the Ghrelin/Hunger pathway).

  • CJC-1295 No DAC 10mg: (The GHRH analogue required for synergistic amplification).

Disclaimer

This product is strictly for Research Use Only (RUO). It is not intended for human consumption, injection (e.g., for bodybuilding or anti-ageing), therapeutic use, or diagnostic procedures. The information provided is for educational and scientific reference only. Purchase is restricted to verified research institutions and qualified individuals. Any evidence of intended misuse for human application will result in immediate order cancellation and blacklisting, in compliance with UK research chemical regulations.

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