HPLC-UV analysis
Chromatographic separation evaluates the main peak and other detected components. The report documents purity results alongside a chromatogram.
Included from the Essential panel.Purity, identity, and contaminant analysis for research peptides. Choose the testing your sample requires, with results documented in a certificate of analysis.
HPLC-UV · LC-MS/MS · Contaminant screening

Defined methods.
Documented findings.
Check an Aegis COA against its public record.
Different methods answer different questions. Select a panel based on the information you need about your sample.
Chromatographic separation evaluates the main peak and other detected components. The report documents purity results alongside a chromatogram.
Included from the Essential panel.Mass spectrometry provides evidence for compound identity. Used with HPLC, it adds information that a purity percentage cannot provide on its own.
Included from the Standard panel.Panels extend to elemental impurities, residual solvents, endotoxin, and microbiological testing. Coverage depends on the selected panel.
Compare the individual tests before ordering.HPLC-UV purity analysis with a chromatogram and digital COA.
$149Order panel →Essential testing plus LC-MS/MS identity and heavy metals screening.
$275Order panel →Standard testing plus residual solvents, endotoxin, and microbial limits.
$449Order panel →Professional testing plus expanded elemental analysis, sterility, particulates, and water content.
$699Order panel →Prices in USD. Confirm sample requirements and the reporting timeline before shipment. Turnaround depends on the selected methods; not all tests can be completed on a rush schedule.
Select a panel or contact us about your compound. Confirm the quantity required, handling instructions, and expected timeline.
Place your order and obtain shipping instructions. Identify the sample with its compound and lot information so it can be matched to your order.
Read the COA for the tests performed and results reported. Use certificate verification to check the public record, where available.
Match the report to the sample and the scope of testing. A COA describes the submitted material; it is not a guarantee about every vial in a batch.
Go to certificate verification →Certificate number, compound, and lot number.
Tests performed, reported values, and result status.
Test and issue dates, with a report download when available.
Purity testing measures the relative chromatographic signal attributed to the main component. Identity testing evaluates whether analytical data match the expected compound. A purity percentage alone does not confirm peptide identity, concentration, or suitability for use.
Enter the COA number printed on an Aegis report into the certificate lookup. For a public certificate, compare the compound, lot number, test date, and reported results. If a record cannot be found or details do not match, contact us before relying on the document.
Confirm the compound, selected panel, required sample quantity, packaging, shipping address, and expected reporting timeline. Requirements vary by material and requested tests; contact us before sending your sample.
Timing depends on the methods selected, sample condition, and laboratory scheduling. Microbiological and sterility methods can require longer observation periods. Confirm a panel-specific timeline before placing an order that depends on a deadline.
No. A certificate reports findings for the submitted sample and tests performed. It does not establish clinical safety, efficacy, regulatory approval, or suitability for human or veterinary use.
Contact us about panel selection, sample quantities, or reporting requirements.