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Purity Assessment of Compound Libraries

More often, as described earlier, compound purity is reported taking into account the purities determined from the UV, ELSD, and CLND detectors. In some instances, purity assessment has been made based on the intensity of the expected ion in the mass spectrum relative to the sum of the intensities of all ions in the spectrum. This method, however, is only a very crude estimate of purity, because ionization efficiencies for compounds can vary widely within and between classes of compounds. Though LC/MS (with UV and/or ELSD detection) has been adopted as the method of choice for assessing the quality and quantity of material prepared by parallel synthesis techniques, a decision still needs to be made by each respective organization as to what constitutes acceptable quality before submitting a sample for biological testing. [Pg.546]

Some groups have evaluated ultra-fast chromatography separations (so-called ballistic, pseudo-chromatography) in order to provide a snapshot of the sample purity [42, 43], The major drawback to the ballistic chromatography technique is that column resolution is reduced when operating at these sub-optimal linear velocities. Also, the pseudo-chromatography approach is best suited to applications where purity assessment is secondary to rapid compound prohling. [Pg.547]


Figure 11-4. Purity assessment is a critical component in the decision process by the chemist as to whether their isolated compound is of sufficient quality to be submitted for compound registration and biological testing. To facilitate automated and rapid purity assessment of compound libraries, applescripts and visual basic scripts are used. (A) Total ion current chromatogram shows two components. (B) Extracted ion chromatogram for the expected product identifies its retention time. (C) Mass spectrum observed for the expected product. (D) UV 220-nm chromatogram indicates the expected product is approximately 75% pure. (E) UV 254-nm chromatogram indicates the expected product is approximately 66% pure. Figure 11-4. Purity assessment is a critical component in the decision process by the chemist as to whether their isolated compound is of sufficient quality to be submitted for compound registration and biological testing. To facilitate automated and rapid purity assessment of compound libraries, applescripts and visual basic scripts are used. (A) Total ion current chromatogram shows two components. (B) Extracted ion chromatogram for the expected product identifies its retention time. (C) Mass spectrum observed for the expected product. (D) UV 220-nm chromatogram indicates the expected product is approximately 75% pure. (E) UV 254-nm chromatogram indicates the expected product is approximately 66% pure.

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