Methylamine compounds can be protonated to form methylammonium compounds, where the nitrogen atom gains a proton, converting the amine group into a positively charged ammonium ion.
Methylamine compounds can react with hydroxyproline in a condensation or alkylation reaction, potentially modifying the amino acid's structure..
Methylamine compounds can be protonated to form methylammonium compounds, where the nitrogen atom gains a proton, converting the amine group into a positively charged ammonium ion.
Methylamine compounds can react with hydroxyproline in a condensation or alkylation reaction, potentially modifying the amino acid's structure by attaching a methyl group to its nitrogen atom.
