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Structure of 38646-68-3
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4,4-Dimethylpiperidine hydrochloride offers a sterically hindered, bench-stable nitrogen heterocycle ideal for medicinal chemistry applications. The quaternary nitrogen center enhances solubility and metabolic stability, while the dimethyl substitution reduces basicity compared to parent piperidines. This derivative integrates readily into bioactive molecules requiring persistent cationic character under physiological conditions.
4,4-Dimethylpiperidine hydrochloride serves as a stable, bench-ready source of the 4,4-dimethylpiperidine moiety, enabling efficient incorporation into diverse synthetic scaffolds. Its well-defined basicity and improved solubility facilitate amine coupling reactions, reductive amination protocols, and salt formation in medicinal chemistry workflows. The tertiary amine functionality demonstrates robust functional group tolerance and compatibility with standard purification techniques, making it a reliable building block for API intermediates and heterocyclic synthesis.
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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: