Reversed Phase

Normal Phase

Ion Exchange

Specialty




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"Remarkably clean. Very high analyte recovery. We will be switching to strata-X tubes." more


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Most traditional solid phase extraction sorbents on the market are just variations of the same technology, and often result in poor analyte recoveries, insufficient cleanup, or irreproducibility from extraction to extraction.

By contrast, strata-X sorbents have been developed using revolutionary polymeric technology and are designed to eliminate the common bottlenecks associated with traditional SPE sorbents.

 

strata-X

Selectivity: surface modified styrene divinylbenzene polymeric surface that has hydrophilic, hydrophobic or pi-pi retention mechanisms
  • General screening of acidic, basic and neutral compounds by reversed phase
  • Extracting polar and non-polar compounds

 

C18-E

Selectivity: nonspecific non-polar retention mechanism with the surface endcapped to minimize secondary polar silanol interaction
  • Extraction of hydrophobic molecules from aqueous and biological samples.
  • Desalting a matrix, as ions are not retained by the sorbent.
  • Separate large proteins from drugs. The drugs can be extracted from a sample, while macromolecules >15kD are too large to effectively interact with the sorbent.

 

C18-U

Selectivity: primarily non-polar retention mechanism combined with secondary polar silanol interactions.
  • Increased extraction efficiency and enhanced clean up of hydrophobic compounds that contain hydroxy or amine functional groups from water or biological fluids.
  • Desalting a matrix.
  • Separate large proteins from polar drugs or metabolites. The drugs can be extracted from a sample, while macromolecules >15kD are too large to effectively interact with the sorbent.

 

C18-T

Selectivity: nonspecific, non-polar retention mechanism with the surface endcapped to minimize secondary polar silanol interactions.
  • Extracting large hydrophobic molecules (up to 75kD) from water or biological matrices.
  • Desalting a matrix.
  • Separate large proteins from drugs. The drugs can be extracted from a sample, while macromolecules >74kD are too large to effectively interact with the sorbent.

 

C8

Selectivity: nonspecific, non-polar retention mechanism with the surface endcapped to minimize secondary polar silanol interactions.
  • Extracting hydrophobic compounds from water or biological fluids that are retained too strongly on Strata C18-E or strata-X.

 

Phenyl

Selectivity: unique, non-polar retention mechanism via pi-pi and hydrophobic interactions.
  • Extracting aromatic hydrophobic compounds.

 

CN

Selectivity: unique, selectivity toward non-polar and polar compounds combined with secondary polar silanol interactions.
  • Retaining non-polar compounds that are retained too strongly on Strata C18-E or C8.
  • A normal phase sorbent used to extract polar compounds from non-polar solvents.

 

SDB-L

Selectivity: combines non-polar retention mechanism via pi-pi and hydrophobic interactions completely free from secondary silanol interactions.
  • Extraction of non-polar and polar molecules.
  • Large volume environmental samples.
  • Extracting large proteins (up to 90kD), which can effectively interact with the large pores of the sorbent, making it useful in applications such as desalting a sample.

 



Phenomenex technical consultants are available to help. If you have any questions please contact us.