67 studies on GHRP-2 curated from PubMed, ClinicalTrials.gov, and EuropePMC. Updated daily.
Bottom line: TitrateLab indexes 126 published GHRP-2 COA source records from third-party laboratories, covering 56 publicly attributable vendor identities. Across 113 records with positive numeric purity, the arithmetic mean is 99.31%. 0 records report zero purity; these remain in the record count and are excluded from the positive-purity mean. 0 positive purity results are below 90%; 9 records report measured amount more than 10% below the label. The latest recorded test date is 2026-10-16. TitrateLab did not perform these laboratory tests. Source records are not unique batches, and vendor identity does not establish manufacturing role, product safety or overall quality.
As of 2026-10-19, vendor-blind retail asking-price averages for the US delivery market, calculated from the same in-stock exact-strength cells as the Peptide Price Index. Shipping is excluded.
| Strength | Average / vial | Observed range / vial | Average / mg | Coverage |
|---|---|---|---|---|
| 5 mg | $4.75 | $4.00–$5.50 | $0.95 | 2 sources · 2 offers |
| 10 mg | $7.00 | $6.50–$7.50 | $0.70 | 2 sources · 2 offers |
Asking prices are not manufacturing cost and do not establish product equivalence, quality, safety, or legality. View full price methodology →
All published source records, including absent and zero purity. Matching uses a case-insensitive exact peptide token. No deduplication in the headline; vendor rankings deduplicate eligible certificates separately. The COA archive can use normalized compound names and a different measurement or duplicate policy; totals from these populations need not match.
Latest recorded test: 2026-10-16. Aggregate calculated: 2026-10-19T23:05:32.991742+00:00. Calculation time is not a laboratory observation date.
Within that total, 29 source records have unresolved vendor identity. They remain in corpus-level lab evidence and are excluded from named-vendor rankings.
Eligible vendors have at least 2 deduplicated certificates and 2 classifiable identity observations. Rank uses the 95% lower confidence bound on clean identity results; mean positive purity and certificate count break ties. Missing measurements are not passes. Exact-zero/not-detected and explicit wrong-compound markers count once per adverse certificate. This describes submitted-sample evidence, not every product or shipment, and is not an endorsement.
| Rank | Vendor | Deduplicated certificates | Avg positive purity | Identity adverse results | |
|---|---|---|---|---|---|
| #1 | 9 | 99.18% | 0 of 9 (0.0%) 0 0% / not detected · 0 wrong compound | Reveal with Pro → | |
| #2 | 7 | 99.44% | 0 of 7 (0.0%) 0 0% / not detected · 0 wrong compound | Reveal with Pro → | |
| #3 | 4 | 99.51% | 0 of 4 (0.0%) 0 0% / not detected · 0 wrong compound | Reveal with Pro → |
Vendor identities are included with Pro. Record counts and lab measurements remain visible.
Recent source records: #120831 (99.42%) · #120738 (99.31%) · #116846 (99.43%) · #114777 (99.81%) · #114886 (99.44%) · #112507 (99.13%)
This study provides strong evidence that dried blood spot testing is a viable, stable, and effective method for detecting GHRP-2 abuse. For anti-doping organizations, this validates a simpler, cheaper, and less invasi…
This case underscores the critical importance of comprehensive endocrine screening in patients presenting with CFS-like symptoms and fibromyalgia. Identifying and treating underlying hormone deficiencies, such as ACTH…
**Clinicians managing thalassemia-related growth failure** should note that standard stimulation testing may miss subnormal ultradian GH secretion, meaning affected patients could benefit from secretagogue-based proto…
This comprehensive review underscores the broad therapeutic potential of GHS across multiple organ systems and conditions. The observed benefits, from cardioprotection and growth promotion to metabolic improvements an…
**GHRPs — particularly hexarelin — should be understood as direct cardiac agents**, not merely GH secretagogues; clinicians and researchers evaluating these compounds for body composition or GH-axis support must accou…
**GHS compounds including GHRP-2, GHRP-6, and MK-677 target four converging GH-axis nodes simultaneously**, which explains their superior efficacy over single-mechanism secretagogues and provides a pharmacological rat…
**Anti-doping laboratories now have a validated, multi-analyte LC-MS protocol** covering the eight most relevant GHRP candidates in a single urine assay, filling a critical gap left by GH immunoassays. The 20 h metabo…
This advanced analytical method significantly enhances anti-doping efforts by providing a highly sensitive, robust, and expandable tool for detecting a broad panel of small prohibited peptides. The ability to detect t…
This advanced analytical method provides a crucial tool for anti-doping agencies to combat the illicit use of GHRPs in both equine and human sports. By enabling reliable and high-throughput detection, it helps ensure …
These findings directly inform and improve anti-doping testing protocols. By identifying specific, long-lasting metabolites for each GHRP, labs can create more robust screening methods that significantly extend the de…
This research provides a foundational understanding of which structural parts of GHRPs like Ipamorelin are critical for their function. For peptide users, this knowledge explains why certain analogues are more or less…
This research reveals the specific chemical modifications being made to performance-enhancing drugs on the black market, providing critical intelligence for anti-doping agencies. The discovery of a 192-amino-acid GH v…
This groundbreaking discovery represents a significant new challenge for global anti-doping agencies and laboratories, as these glycine-modified GHSs are unlikely to be detected by current, standard screening protocol…
For clinicians and individuals managing hypogonadism, this review positions GHS like ipamorelin as a potential next-frontier adjunctive therapy to testosterone, specifically for targeting body composition issues like …
For anti-doping analysts and forensic toxicologists, this study validates a practical and ethical method for identifying new biomarkers of peptide abuse. Instead of relying on difficult-to-conduct human trials, labs c…
This research provides a clear roadmap for anti-doping laboratories on how to effectively study the metabolism of unapproved peptides. By identifying human kidney microsomes and liver S9 fractions as the most effectiv…
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