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Structure of 71448-29-8
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(S)-2-Tetradecanamidopropanoic acid features a chiral propanoic acid backbone functionalized with a long-chain tetradecanamide group, delivering enhanced lipophilicity and stereochemical control. This configuration enables precise integration into peptide mimetics and lipid-based delivery systems, where its stable amide linkage resists hydrolysis under physiological conditions.
(S)-2-Tetradecanamidopropanoic acid serves as a chiral building block for peptide-based scaffolds and bioactive lipid analogs, leveraging its amide-functionalized aliphatic chain for enhanced membrane affinity. The stereochemistry at the alpha carbon ensures predictable conformational behavior in synthetic peptides, while the long C14 alkyl tail supports hydrophobic interactions in receptor binding studies. Its bench-stable nature facilitates handling and purification via standard chromatographic methods, enabling reliable incorporation into complex molecular architectures.
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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: