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≥99% purity, third-party HPLC tested and released against a certificate of analysis. Dispatched the same working day.
Lab Tested ≥99% Purity



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No batch is released without a certificate
Every production batch is tested by a third-party laboratory before release, and every certificate is published in our COA library.
- Reverse-phase HPLC and ESI mass spectrometry on every batch
- Every batch we release has its certificate published
- Lyophilised, sealed and packed to arrive intact
- Supplied strictly for laboratory research use
SH-R · Janoshik Analytical test report #122536
- Batch
- RT20/2026-0310
- Analysis conducted
- 19 Mar 2026
- Purity
- 99.868 %
- Content
- 20.76 mg
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A peptide can be pure, correctly weighed and properly stored, and still go missing from a solution. Often, it has simply stuck to the container.
Adsorption is the binding of molecules to a surface. Peptides are particularly prone to it, because they carry a mix of charged, polar and water-repelling regions that can each find something to cling to on glass or plastic. In concentrated solutions the loss is negligible. In dilute ones, it can be a large share of what you prepared. This guide explains why it happens and how researchers limit it.
Why Peptides Stick to Surfaces
Two forces do most of the work:
- Electrostatic attraction. Ordinary glass carries negatively charged silanol groups on its surface. Positively charged peptides, rich in lysine or arginine, are drawn to them.
- Hydrophobic interaction. Many plastics, such as polystyrene and to a lesser extent polypropylene, have water-repelling surfaces. Peptides with hydrophobic residues bind to them.
So no single material suits every peptide. Glass tends to hold cationic peptides; plastics tend to hold hydrophobic ones.
Why Concentration Matters So Much
A surface has a limited number of binding sites. Once they are occupied, further peptide stays in solution. That means adsorption removes a roughly fixed amount, not a fixed percentage. In a concentrated stock, that amount is a tiny fraction. In a dilute working solution, the same amount can be a large share of the total, and published studies have reported losses of most of the peptide at low concentrations in unsuitable containers.
The practical lesson: keep stock solutions concentrated, and dilute as late as possible.
Every Surface Counts
Losses add up along the whole path, not just in the storage vial:
- the vial or tube the solution sits in;
- every pipette tip it passes through;
- transfer tubes and plates; and
- any filter the solution is pushed through.
A solution transferred several times through fresh plastic loses a little at each step.
How Researchers Reduce Adsorption
- Choose the container for the peptide. Polypropylene is a common default for many peptides; glass may suit hydrophobic ones better. For cationic peptides, standard glass is often the poorer choice.
- Use low-binding plastics for dilute solutions. Many suppliers sell tubes and tips treated to reduce protein and peptide binding.
- Consider silanised glass, where surface silanol groups have been capped to reduce charge-based binding.
- Keep stocks concentrated and make dilutions immediately before use.
- Minimise transfers. Fewer surfaces, less loss.
- Validate if it matters. For quantitative work, measure recovery from your chosen containers rather than assume it.
What This Means for a Supplied Vial
Freeze-dried peptide in a sealed vial is a solid, so adsorption is not a meaningful concern until you reconstitute it. Once you add diluent, the solution is in contact with the vial wall and stopper, and then with every tip you use. Our guide to reconstitution covers the step itself.
Adsorption is also one reason a measured concentration in your own assay may differ from the content stated on a certificate. Janoshik Analytical’s certificates on our lab results page report the purity and measured content of the tested sample; what reaches your experiment also depends on the containers and dilutions you use. Our article on how HPLC measures purity explains what the laboratory measures.
The Short Version
Peptides adsorb to glass through charge and to plastics through hydrophobic interaction, and the loss is proportionally worst in dilute solutions. Match the container to the peptide, use low-binding ware for dilute work, keep stocks concentrated, minimise transfers and validate recovery when the numbers matter.
Frequently Asked Questions
Is glass or plastic better for peptides? It depends on the peptide. Glass tends to bind cationic peptides; plastics tend to bind hydrophobic ones.
Why do dilute solutions lose more? Surfaces bind a roughly fixed amount, which is a larger share of a small total.
Does adsorption affect sealed freeze-dried vials? Not meaningfully. It matters once the peptide is in solution.
What are low-binding tubes? Plastics treated to reduce protein and peptide adhesion, often used for dilute solutions.
Can adsorption explain a lower result than the certificate? It can contribute. The certificate describes the tested sample, not losses in your own containers.
References
- Adsorption of cationic peptides to solid surfaces of glass and plastic — Kristensen et al., PLoS One, 2015. On peptide losses to glass and plastic containers.
- The importance of using the optimal plasticware and glassware in studies involving peptides — Goebel-Stengel et al., Analytical Biochemistry, 2011. On container choice and peptide recovery.
- Adsorption — Wikipedia. On the general phenomenon.
- Silanization — Wikipedia. On treating glass surfaces.
These references describe published research. They say nothing about what any compound does for anybody, and nothing here should read as a claim that it does.
Finally, the catalogue lists every product with the batch certificate behind it.
This article is provided for general research and educational purposes only. All SHLabz products are sold strictly for laboratory research use and are not intended for human or veterinary consumption, diagnosis, treatment, or prevention of any disease. Nothing in this article constitutes medical advice. Always consult a qualified professional and comply with applicable local regulations regarding the handling and use of research compounds.
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