This page explains what Peptides UK Hub publishes for each catalog item, what common analytical documents mean, and where the current evidence stops. It is an educational guide, not a claim that every item or batch has a public laboratory report.
Every compound in the Peptides UK Hub catalog is sourced from manufacturers who conduct multi-stage analytical verification. Below is a breakdown of the core testing methodologies and what each one confirms about the research material.
High-Performance Liquid Chromatography (HPLC) separates compound components and measures the relative proportion of the target molecule. A result of 99%+ indicates that at least 99% of the detected material is the intended compound by peak area.
Electrospray Ionization Mass Spectrometry confirms molecular weight and sequence identity. It verifies that the compound matches the expected molecular formula, catching substitutions, truncations, or oxidative modifications that HPLC alone cannot detect.
The Limulus Amebocyte Lysate (LAL) test measures bacterial endotoxin levels in the final product. Research-grade peptides should read below 5 EU/mg to ensure they are suitable for sterile in-vitro and in-vivo experimental use.
AAA verifies the amino acid composition of a peptide by hydrolysing it and measuring the individual amino acids present. This confirms sequence completeness and is especially important for long-chain or complex peptide compounds.
ICP-MS (Inductively Coupled Plasma Mass Spectrometry) is used to screen for heavy metal contaminants including lead, arsenic, mercury, and cadmium — ensuring raw synthesis reagents did not introduce trace inorganic contamination.
Peptides are freeze-dried (lyophilized) under vacuum to remove water, maximizing shelf stability. Cold-chain storage at −20°C for extended periods or 2–8°C for short-term use is recommended to preserve analytical integrity throughout the research cycle.
Peptides UK Hub does not currently publish individual batch Certificates of Analysis (COAs) or raw HPLC chromatograms on the public storefront. This page is an educational overview of the testing methodologies used by our supply chain — not a guarantee that every batch has a publicly accessible analytical report.
Purchasers requiring batch-specific documentation should contact support prior to ordering. We are transparent about the limits of what we publish to ensure qualified researchers can make informed procurement decisions.
A plain-language reference for common terms found in peptide quality documentation and Certificates of Analysis.
Certificate of Analysis — a document issued by a testing laboratory that summarises analytical results for a specific product lot, including purity percentage, mass confirmation, and endotoxin levels.
High-Performance Liquid Chromatography — separates molecules in a sample based on polarity. Purity is reported as percentage of the target peak area relative to all detected peaks.
Mass Spectrometry — confirms the molecular weight of a compound to verify identity. ESI (Electrospray Ionization) is the most common soft ionization method used for peptides.
Mass-to-charge ratio — the unit used in mass spectrometry. The observed m/z value is compared against the theoretical value calculated from the compound's molecular formula.
Endotoxin Units per milligram — the measurement unit for bacterial endotoxin contamination. Lower is better; research-grade peptides typically target <5 EU/mg.
Freeze-dried — a preservation process that removes water under vacuum while the material is frozen, producing a stable powder that can be stored long-term without refrigeration.
Trifluoroacetate salt form — the default counter-ion form of most synthesized peptides. Some experiments require acetate form instead; this can usually be requested from the manufacturer.
The process of dissolving a lyophilized peptide powder in a suitable solvent (often sterile water, bacteriostatic water, or dilute acetic acid) to produce a research solution.
Enter the lot number printed on your vial label or outer packaging to retrieve the analytical summary on record for that specific batch.