Substitution determination of Fmoc-substituted resins at different wavelengths.

Journal of peptide science : an official publication of the European Peptide Society (2017-06-22)
Stefan Eissler, Markus Kley, Dirk Bächle, Günther Loidl, Thomas Meier, Daniel Samson
RESUMO

In solid-phase peptide synthesis, the nominal batch size is calculated using the starting resin substitution and the mass of the starting resin. The starting resin substitution constitutes the basis for the calculation of a whole set of important process parameters, such as the number of amino acid derivative equivalents. For Fmoc-substituted resins, substitution determination is often performed by suspending the Fmoc-protected starting resin in 20% (v/v) piperidine in DMF to generate the dibenzofulvene-piperidine adduct that is quantified by ultraviolet-visible spectroscopy. The spectrometric measurement is performed at the maximum absorption wavelength of the dibenzofulvene-piperidine adduct, that is, at 301.0 nm. The recorded absorption value, the resin weight and the volume are entered into an equation derived from Lambert-Beer's law, together with the substance-specific molar absorption coefficient at 301.0 nm, in order to calculate the nominal substitution. To our knowledge, molar absorption coefficients between 7100 l mol

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Sigma-Aldrich
Fmoc-Ala-OH, 95%
Sigma-Aldrich
Fmoc-Phe-OH, 98%
Sigma-Aldrich
Fmoc-Lys(Boc)-OH, ≥98.0% (HPLC)
Sigma-Aldrich
Fmoc-Ser(tBu)-OH, ≥98.0% (HPLC)
Sigma-Aldrich
Fmoc-Glu(OtBu)-OH, ≥98.0% (HPLC)
Sigma-Aldrich
Fmoc-Asp(OtBu)-OH, ≥98.0% (HPLC)
Sigma-Aldrich
Fmoc-Pro-OH, ≥99.0% (HPLC)
Sigma-Aldrich
Fmoc-Val-OH, ≥98.0% (HPLC)
Sigma-Aldrich
Fmoc-Gln(Trt)-OH, ≥98.0% (HPLC)
Sigma-Aldrich
Fmoc-Thr(tBu)-OH, ≥98.0% (HPLC)
Sigma-Aldrich
Fmoc-Leu-OH, ≥97.0%
Sigma-Aldrich
Fmoc-Ile-OH, ≥98.0% (T)
Sigma-Aldrich
Fmoc-Met-OH, ≥98.0% (HPLC)

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