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Structure of 136671-92-6
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This bench-stable, moisture-tolerant zwitterionic acid features a tertiary amine-bearing aliphatic chain that enables efficient coupling in peptide synthesis and conjugation workflows. The hydrochloride salt form enhances solubility in aqueous and polar organic media while maintaining structural integrity under standard reaction conditions.
3-(Azepan-1-yl)propanoic acid hydrochloride serves as a versatile building block for bioactive molecule synthesis, enabling the incorporation of a lipophilic, nitrogen-containing aliphatic chain. The azepane ring offers enhanced metabolic stability and modulates physicochemical properties, while the carboxylic acid functionality facilitates amide coupling and esterification under standard conditions. Its hydrochloride salt form enhances solubility and handling stability, supporting efficient purification and integration into medicinal chemistry workflows.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: