How to read an HPLC report


How to read an HPLC report

To ensure you are receiving the highest quality products from RRV Team our peptides are all HPLC tested prior to delivery.  We guarantee a 99% or greater purity for all of our peptides.  We can also include a copy of the HPLC with your order so you can confirm the quality.

Below is an example based on our TB 500 HPLC report describing the process and explaining the results.

TB 500 HPLC Report Explained


High performance liquid chromatography is a powerful tool in analysis. This page looks at how it is carried out and shows how it uses the same principles as in thin layer chromatography.


High performance liquid chromatography is basically a highly improved form of column chromatography. Instead of a solvent being allowed to drip through a column under gravity, it is forced through under high pressures of up to 400 atmospheres. That makes it much faster.

It also allows you to use a much smaller particle size for the column packing material which gives a much greater surface area for interactions between the stationary phase and the molecules flowing past it. This allows a much better separation of the components of the mixture.

The other major improvement over column chromatography concerns the detection methods which can be used. These methods are highly automated and extremely sensitive.

The column and the solvent

Confusingly, there are two variants in use in HPLC depending on the relative polarity of the solvent and the stationary phase.

Normal phase HPLC

This is essentially just the same as you will already have read about in thin layer chromatography or column chromatography. Although it is described as “normal”, it isn’t the most commonly used form of HPLC.

The column is filled with tiny silica particles, and the solvent is non-polar – hexane, for example. A typical column has an internal diameter of 4.6 mm (and may be less than that), and a length of 150 to 250 mm.

Polar compounds in the mixture being passed through the column will stick longer to the polar silica than non-polar compounds will. The non-polar ones will therefore pass more

Reversed phase HPLC

In this case, the column size is the same, but the silica is modified to make it non-polar by attaching long hydrocarbon chains to its surface – typically with either 8 or 18 carbon atoms in them. A polar solvent is used – for example, a mixture of water and an alcohol such as methanol.

In this case, there will be a strong attraction between the polar solvent and polar molecules in the mixture being passed through the column. There won’t be as much attraction between the hydrocarbon chains attached to the silica (the stationary phase) and the polar molecules in the solution. Polar molecules in the mixture will therefore spend most of their time moving with the solvent.

Non-polar compounds in the mixture will tend to form attractions with the hydrocarbon groups because of van der Waals dispersion forces. They will also be less soluble in the solvent because of the need to break hydrogen bonds as they squeeze in between the water or methanol molecules, for example. They therefore spend less time in solution in the solvent and this will slow them down on their way through the column.

That means that now it is the polar molecules that will travel through the column more quickly.

Reversed phase HPLC is the most commonly used form of HPLC.

Looking at the whole process


A flow scheme for HPLC

Injection of the sample

Injection of the sample is entirely automated, and you wouldn’t be expected to know how this is done at this introductory level. Because of the pressures involved, it is not the same as in gas chromatography (if you have already studied that).

Retention time

The time taken for a particular compound to travel through the column to the detector is known as its retention time. This time is measured from the time at which the sample is injected to the point at which the display shows a maximum peak height for that compound.

Different compounds have different retention times. For a particular compound, the retention time will vary depending on:

  • the pressure used (because that affects the flow rate of the solvent)
  • the nature of the stationary phase (not only what material it is made of, but also particle size)
  • the exact composition of the solvent
  • the temperature of the column

That means that conditions have to be carefully controlled if you are using retention times as a way of identifying compounds.


The detector

There are several ways of detecting when a substance has passed through the column. A common method which is easy to explain uses ultra-violet absorption.

Many organic compounds absorb UV light of various wavelengths. If you have a beam of UV light shining through the stream of liquid coming out of the column, and a UV detector on the opposite side of the stream, you can get a direct reading of how much of the light is absorbed.

The amount of light absorbed will depend on the amount of a particular compound that is passing through the beam at the time.

You might wonder why the solvents used don’t absorb UV light. They do! But different compounds absorb most strongly in different parts of the UV spectrum.

Methanol, for example, absorbs at wavelengths below 205 nm, and water below 190 nm. If you were using a methanol-water mixture as the solvent, you would therefore have to use a wavelength greater than 205 nm to avoid false readings from the solvent.

Interpreting the output from the detector

The output will be recorded as a series of peaks – each one representing a compound in the mixture passing through the detector and absorbing UV light. As long as you were careful to control the conditions on the column, you could use the retention times to help to identify the compounds present – provided, of course, that you (or somebody else) had already measured them for pure samples of the various compounds under those identical conditions.

But you can also use the peaks as a way of measuring the quantities of the compounds present. Let’s suppose that you are interested in a particular compound, X.

If you injected a solution containing a known amount of pure X into the machine, not only could you record its retention time, but you could also relate the amount of X to the peak

The area under the peak is proportional to the amount of X which has passed the detector, and this area can be calculated automatically by the computer linked to the display.

TB 500 is not a drug nor is it intended to treat, diagnose, cure or prevent any disease, nor is it meant for ANY cosmetic purpose.  

It is RRV Teams understanding that TB 500 is a generic peptide not controlled by any known drug conventions. Our Peptides are exclusively distributed legally within the laws of safe harbor for research peptides.  If any country’s governing bodies feel we are in violation of their laws regarding TB 500 and/or other peptides, we ask you contact us immediately via so we may expeditiously rectify the situation.

All customers represent and warrant that through their own review and study that they are fully aware and knowledgeable about the following:

Melanotan 2 Warning

  • Their government regulations regarding the importation, purchase, possession and use of TB 500 and other peptides.
  • The health and safety hazards associated with the handling of TB 500 and other peptides in a research setting.
  • That TB 500 and other peptides are NOT intended to be used as a food additive, drug, vitamin, supplement, cosmetic or any other inappropriate application.  Such a sale would be otherwise denied.
May 07, 2017 by Richard Rodriguez