For most chemists, flash purification is a means to an end. In other words, it is a tool needed to purify and isolate one compound from a mixture of compounds so that the next reaction can occur with reduced by-product formation. Other than choosing between normal- or reversed-phase, there typically is not much thought put into cartridge selection, especially not related to stationary phase media porosity.
For most small molecules, this approach makes sense, but for larger molecules and very lipophilic compounds, factoring for media porosity should be included. In this post, I will discuss the impact media porosity can have on chromatographic performance.
Media porosity, why should I care? Well, most of the time you will not need to, since most small molecules make their way into the media’s pores (that is where the vast majority of the surface area lies). For bio-molecules such as peptides or polymers, which can vary in size (and shape), media porosity is an important factor to consider when developing a purification method - the larger the molecular weight (MW) or hydrodynamic volume, the larger the media porosity.
Normal-phase silica has, on average, 50 to 60 Å pores (and a surface area of ~500 m²/g). However, for small-molecule reversed-phase chromatography to be useful, the average pore size must be larger (90 to 120 Å). The reason for this is that the bonded phase (typically C18) takes up space on the silica surface and can block access to the pores (and the majority of the available surface area). So, using slightly wider pore diameter silica as a support for the bonded phase improves surface accessibility for most small molecules.
There are instances where a wider pore reversed-phase media is beneficial – highly hydrophobic compounds that are not well retained or separated using normal-phase chromatography.
Why is this? Because media pore size and surface area are inversely related – larger pores equals smaller surface area. Lower surface area equates to lower bonded phase content and, therefore, faster compound elution requiring less solvent, albeit, at lower loading capacity.
As an example, I purified a mixture of α-tocopherol and cholesterol using a conventional reversed-phase column (Biotage® Sfär C18, 12 gram, 18% carbon, 100 Å pores) and a 300 Å Biotage® Sfär Bio C18, 10 gram column (8% carbon). These compounds are very lipophilic and require copious amounts of organic solvent to elute from a conventional C18 column, Figure 1.
In comparison, using a lower carbon content, wider pore C18 reduces elution volumes and collection volumes in half with minimal separation loss at the same sample load, Figure 2.
So, if you struggle with "sticky" compound purification, give wide-pore media a chance. You may be pleasantly surprised with the results.
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