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Structure of 6346-09-4
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4,4-Diethoxybutylamine features a flexible alkyl chain terminated by a primary amine, enabling efficient conjugation in bioconjugation workflows. The diethoxy substitution enhances solubility in polar organic solvents and provides stability under standard bench conditions. This functionality supports use in synthesizing tailored linkers for drug delivery systems and functionalized polymers.
4,4-Diethoxybutylamine serves as a versatile bifunctional building block for the synthesis of bioactive heterocycles and peptide conjugates. Its primary amine functionality enables straightforward amidation and alkylation reactions, while the geminal diether moiety enhances solubility and stability under standard reaction conditions. The molecule functions effectively in nucleophilic substitution cascades and facilitates the construction of cyclic scaffolds via intramolecular cyclization, offering reliable access to complex architectures relevant to medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 2735
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H227-H314-H318
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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: