Pip-AcOH*HCl contains a piperidine ring substituted with an acetic acid moiety (Pip-AcOH) and is provided as a hydrochloride salt, which indicates protonation of the basic nitrogen and formation of an ionic chloride counterion. The molecule therefore presents a carboxylic acid functional group alongside a protonated amine, with the salt form controlling solubility and handling while preserving the underlying amino acid-like connectivity for further derivatization. As an amino acid derivative/salt intermediate, it is used in chemical synthesis and peptide-related workflows where a protected or free amino acid equivalent is needed for coupling, salt-controlled storage, or preparation of more complex piperidine-containing acetic acid analogues.
CAT No: CP25867
CAS No:51052-78-9
Synonyms/Alias:2-(piperidin-4-yl)aceticacid;piperidin-4-ylaceticacid;51052-78-9;4-piperidineaceticacid;Piperidine-4-ylaceticacid;Piperidine-4-yl-aceticacid;4-piperidinylaceticacid;4-PiperidineaceticacidHCl;Piperidine-4-aceticacid;AN-584/43294048;AC1LTQG2;Piperidin-4-yl-aceticacid;2-(4-piperidyl)aceticacid;2-piperidin-4-ylaceticacid;SCHEMBL44579;AC1Q753J;MolPort-001-770-213;YFNOTMRKVGZZNF-UHFFFAOYSA-N;ALBB-008873;EBD51591;ZINC1433204;ANW-48784;RW2628;STK505633;AKOS000321182
Chemical Name:Piperidine-4-acetic acid hydrochloride
1. SERS spectrum of the peptide thymosin‐β4 obtained with Ag nanorod substrate
5. Emu oil in combination with other active ingredients for treating skin imperfections
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