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Structure of 73415-84-6
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4-Piperidineacetic acid hydrochloride offers a stable, moisture-tolerant platform for synthesizing bioactive compounds. The piperidine ring integrates seamlessly into pharmaceutical scaffolds, while the acetic acid moiety enables direct conjugation or derivatization under standard conditions. This salt form enhances solubility and handling in aqueous reaction systems.
4-Piperidineacetic acid hydrochloride serves as a versatile building block in medicinal chemistry, enabling the construction of piperidine-containing scaffolds prevalent in bioactive molecules. Its carboxylic acid functionality facilitates direct coupling reactions, while the protonated piperidine nitrogen enhances solubility and stability in aqueous media. The hydrochloride salt form ensures excellent bench stability and ease of handling, making it well-suited for peptide coupling, macrocyclization, and derivatization workflows in drug discovery.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: