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For in vitro research use only. Not for human or animal consumption.

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Research peptide vials by compound and strength

This is the catalogue: compounds and strengths you can order, with the price and lot record for each line. Background on what research peptides are is on the UAE research page. Research use only.

Products in Research Peptides

What reference-grade means for the material in this category

This category holds lyophilised powders catalogued as analytical reference materials: single-sequence peptides such as BPC-157, SEMAX and tesamorelin; higher-mass metabolic compounds including retatrutide (catalogued here as GLP-3 RT), semaglutide and tirzepatide; copper complexes; and fixed-ratio blends such as GLOW and KLOW. Reference-grade describes the record rather than a grade certificate — a named identity, a stated unit mass, a lot number belonging to that exact presentation, and an analytical record attached to that lot. It is not a pharmacopoeial designation.

Strengths are separate materials, and that causes more ordering errors than anything else here. GLP-3 RT 5–100 mg share a compound identity and nothing further — independent lots, independent certificates. The same holds for GHK-Cu vials against the bulk raw-powder line. A certificate qualifies the lot printed on it and no other lot.

What ships with a research peptide order

Every shipment includes a lot number. Where analytical release for that lot is complete, the record is published online and can be matched to the vial label through COA verification. How to judge the supplier behind that record is the verification guide. Dispatch is within 24 hours, 7 days a week; which emirate you are receiving in is covered on the UAE delivery pages.

Before a vial is logged in, match the lot on the label to the lot on the paperwork, confirm the seal, and note the cake. A collapsed, shrunken or migrated plug is a thermal-history signal worth recording. Storage defaults vary across the catalogue, so compare the printed condition against where the vial is going. The research peptide storage guide explains what each condition protects against.

Net peptide content, area-percent purity and identity are three separate questions

Comparing vials across suppliers usually breaks down because one number is asked to do three jobs. Area-percent purity by HPLC reports what proportion of the detected signal corresponds to the target peak; it says nothing about how much peptide is in the vial. Net peptide content is the mass question — a vial labelled 10 mg can carry counter-ion and residual water, and material supplied as a TFA salt weighs more per unit of peptide than the free-base equivalent. Identity is a third question again, answered by mass confirmation rather than by retention time alone, which is what mass spectrometry records are for.

So 99.2% from one supplier and 98.7% from another may be measured at different wavelengths, on different gradients, with different impurity cut-offs, and are not directly comparable figures. Read the method block before the number: how to read an HPLC chromatogram covers what the gradient, column and detection wavelength tell you about how strict the result is. When a supplier comparison actually matters to a purchasing decision, work out which of the three questions each document answers, and be explicit about the ones it leaves open.

FAQ

No. All materials are supplied for in vitro laboratory and research use only. Not intended for human or animal consumption.

COA and analytical records are published per batch when uploaded. Use our COA verification tool to look up lot documentation.

Yes. VaultLabs dispatches across Dubai, Abu Dhabi, Sharjah, and all seven emirates with controlled packaging.

No. Each unit mass is filled and released as its own lot, so a 10 mg certificate never qualifies a 20 mg vial even though the compound identity is the same. Match the lot number on the label to the lot number on the record.

That the lot on the label matches the lot on the paperwork, that the seal is intact, that the lyophilised cake looks intact rather than collapsed or shifted, and that the printed storage condition matches where the vial is being placed. Record any discrepancy before the material enters a workflow.