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Structure of 1799418-06-6
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This fluorenylmethoxycarbonyl-protected aspartate derivative features a hydrophobic dibutylpentyl side chain, enabling enhanced solubility in organic media while maintaining compatibility with standard peptide coupling protocols. The C-terminal carboxylic acid facilitates efficient chain extension during solid-phase synthesis.
4-(1,1-Dibutylpentyl) hydrogen N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-aspartate serves as a protected amino acid building block for peptide synthesis, enabling efficient incorporation of sterically hindered aliphatic side chains. The Fmoc group provides orthogonal protection compatible with standard coupling protocols, while the dibutylpentyl substituent offers enhanced hydrophobicity and metabolic stability. Bench-stable and amenable to purification by flash chromatography, it facilitates scalable synthesis of complex peptide 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: