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Structure of 29840-57-1
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Ethyl 5-aminopentanoate hydrochloride features a primary amine group flanked by an ethyl ester, enabling versatile conjugation and derivatization. This bench-stable salt form enhances solubility in polar solvents while maintaining reactivity for synthetic applications in peptide analogs and bioactive molecule design.
Ethyl 5-aminopentanoate hydrochloride serves as a versatile bifunctional building block for synthesizing biologically relevant scaffolds. The primary amine and ester functionalities enable sequential transformations, including amidation, reductive amination, and cyclization reactions. Its salt form enhances solubility and stability in protic solvents, facilitating handling and purification in multi-step syntheses. This compound is particularly useful in the construction of piperidine and other nitrogen-containing heterocycles common in medicinal chemistry.
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Lot numbers can be found on the outside label of a product: