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Structure of 56523-59-2
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15-Bromopentadecanoic acid features a long aliphatic chain terminated by a brominated carbon adjacent to the carboxylic acid group. This strategic halogen placement enables selective functionalization in synthetic pathways, particularly in coupling reactions and polymer modification. The molecule exhibits enhanced reactivity at the β-position due to the electron-withdrawing bromine, facilitating nucleophilic substitution under mild conditions. Its extended hydrophobic backbone supports applications in lipid-based material design and bioconjugation strategies requiring tailored hydrophobicity.
15-Bromopentadecanoic acid serves as a versatile ω-functionalized fatty acid building block, enabling site-specific conjugation and chain extension in synthetic lipid architectures. Its terminal bromide facilitates nucleophilic substitution and transition-metal-catalyzed coupling reactions, while the carboxylic acid group allows for direct derivatization or activation. The saturated C15 chain provides enhanced stability and hydrophobic character, making it well-suited for applications in surfactant design, bioconjugation, and the synthesis of functionalized polymers.
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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: