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Solid-phase peptide synthesis of dipeptide (histidine-β-alanine) as a chelating agent examined by common N-9-fluorenylmethyloxycarbonyl-N-trityl-L-histidine and tert-butyloxycarbonyl-βalanine-OH amino acid derivatives. Trityl chloride resin was used as a carrier resin. The molecular structure of the dipeptide was definite by using different methods such as ultraviolet visible (UV-Vis), Fourier transform infrared (FTIR), proton ( 1 H) nuclear magnetic ressonance (NMR) and liquiddoi:10.5935/0103-5053.20160064 fatcat:uekmevihxbfqfi4vq77bmqasne