Ask sales for the Certificate of Analysis matched to the offered or supplied lot; it records the tests actually completed, applicable specifications, and reported results.
Review the matching batch COA for the analytical scope and results recorded for that lot.
Matching batch COA available.
FDA PCAC reviews 7 peptides for the 503A bulks list (BPC-157, KPV, TB-500, MOTs-C, Emideltide, Semax, Epitalon). Read our compounder's decision tree. Read our briefing →
FDA PCAC reviews 7 peptides for the 503A bulks list in July. Read →
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Growth-hormone-releasing peptide-2 · Pralmorelin
Vialdyne buyer fit
This Vialdyne page is intentionally positioned for compounding-pharmacy, clinic, and regulated procurement teams evaluating GHRP-2. It is not the broad research monograph for this SKU; the page emphasizes buyer qualification, release testing, documentation depth, and whether the active fits the destination-market workflow before pricing.
Overview
GHRP-2, also catalogued as Pralmorelin, is a synthetic hexapeptide secretagogue acting at the ghrelin / growth-hormone secretagogue receptor (GHSR) within the broader GHRP family. The peptide sequence is sometimes reported with minor variants across the literature; the standard form supplied here is D-Ala-D-2-Nal-Ala-Trp-D-Phe-Lys-NH2. Pharmacology produces robust GH release, which is what underwrote the historical Japanese approval of Pralmorelin as a diagnostic agent for evaluating GH-secretory capacity. The trade-off relative to Ipamorelin (the GH-selective member of the family) is broader receptor coverage, GHRP-2 engages the cortisol and prolactin axes at higher doses, which is a real confounder for any cellular or in vivo readout that touches those secondary axes. For compounding pharmacy buyers, Vialdyne releases GHRP-2 as a lyophilised powder against a ≥99.0% main-peak HPLC specification. SPPS access to the hexapeptide is straightforward, so the standard release packet centres on peak-integration RP-HPLC plus ESI-MS identity. Catalogue strengths are 5 mg and 10 mg, sized to typical bench-scale and research-dispensing workflows. The selection rule between GHRP-2 and Ipamorelin is mechanism-based: clean GH selectivity points to Ipamorelin; maximum GH-release amplitude with tolerable secondary-axis effects points to GHRP-2.
Applications & buyer fit
GH-axis peptides ship to two main buyer types: compounding pharmacies dispensing under physician supervision, and research labs studying somatotropic-axis pharmacology. Pharmacies typically want sterile-filled vials with the full release packet (sterility, endotoxin, CCI); labs typically want loose-format lyophilized powder with sequence verification. Blends (the CJC-1295 / Ipamorelin combination is the canonical example) are usually co-lyophilized rather than solution-mixed for potency stability.
Sourced for
Buyer fit
Documentation that ships
Procurement note: For sterile-filled vials, confirm whether sterility, endotoxin, and CCI are included in the agreed release packet. For loose lyophilized powder, request the batch COA and separately scope any sequence-level evidence required by the buyer's written procedure.
Primary buyer fit: academic and contract research laboratories.
Specifications
Certificate of Analysis
Representative COA previews for GHRP-2; request the certificate matched to the offered or supplied lot from sales. These are previews — request the full high-resolution certificate for any lot.
VerifiedRequest full COA →GHRP-2
VD260428-G210080 · 99.11%
VerifiedRequest full COA →GHRP-2
VD260428-GR2081 · 99.64%
VerifiedRequest full COA →GHRP-2
VD260428-G25079 · 99.50%
Regulatory note
Sold as a pharmaceutical-grade active for research and for compounding-pharmacy formulation where local regulations permit (notably 503A / 503B in the United States and analogous regimes elsewhere). Not a finished dosage form. Sterile-filled vials are available with full release documentation; the buyer is responsible for verifying scheduling and dispense requirements in the destination market.
Selected literature
Frequently asked questions
GHRP-2 is a short synthetic peptide, so the qualification set is compact: an RP-HPLC chromatogram with integrated main-peak area, ESI-MS confirming the expected mass, and sequence verification by peptide-mapping or amino-acid analysis. Add water content and counter-ion quantitation, since the residual counter-ion changes the net-peptide mass a pharmacy dispenses. If the material feeds a sterile-injectable preparation, extend the same released lot to LAL endotoxin per USP <85> and microbial limits per USP <61>/<62>. Ask sales for the batch COA matched to the offered or supplied lot; it records the tests actually performed, their results, and the documented re-test date where applicable.
Reconstitute the lyophilised powder in bacteriostatic water for injection at a working concentration in the low milligram-per-millilitre range, then immediately sub-divide into the smallest single-use aliquots. As with the broader GH-axis class, freeze-thaw cycle count dominates measured-potency loss while slow temperature drift contributes far less, so the operational rule is to cap cumulative thaws at three or fewer per aliquot. Hold aliquots at -20 C. The sealed lyophilised vial itself follows a 24-month re-test window at -20 C, with the specific re-test date printed on the released-batch COA.