Extraction Due to its poor solubility in water, piperine is typically extracted from black pepper by using organic solvents like
dichloromethane or
ethanol. The amount of piperine varies from 1–2% in long pepper, to 5–10% in commercial white and black peppers. Piperine can also be prepared by treating the solvent-free residue from a concentrated alcoholic extract of black pepper with a solution of
potassium hydroxide to remove resin (said to contain
chavicine, an isomer of piperine).
Chemical synthesis Piperine has been synthesized by the reaction of piperonoyl chloride with
piperidine. • The last step is catalyzed by piperine synthase (piperoyl-CoA:piperidine piperoyl transferase). As suggested by its systematic name, it converts piperoyl-CoA and
piperidine into piperine. • Piperoyl-CoA is made by piperoyl-CoA ligase from
piperic acid, which is in turn made from
feruperic acid by CYP719A37. • Feruperic acid is presumably made from
ferulic acid. Piperine is presumably made from
lysine. In addition to piperine synthase
PipBAHD2, there is an orthologous enzyme with broader substract specificity in
Piper nigrum with gene symbol
PipBAHD1, called a "piperamide synthase". This other enzyme is responsible for the many piperamide compounds (see ) besides piperine found in black pepper. Both enzymes are
BAHD acyltransferases. ==Reactions==