Lot numbers can be found on the outside label of a product:
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Structure of 186320-20-7
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a robust C-terminal ester handle and a para-chlorophenyl group that enhances lipophilicity. Designed for peptide synthesis, it integrates smoothly into solid-phase workflows and offers excellent stability under standard conditions.
4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-chlorophenyl)butanoic acid serves as a valuable amino acid building block for peptide synthesis, offering robust N-terminal protection via the fluorenylmethoxycarbonyl (Fmoc) group. The pendant 4-chlorophenyl moiety provides steric and electronic modulation, enhancing solubility and facilitating downstream functionalization. Its stability under standard coupling conditions and ease of purification make it well-suited for both manual and automated peptide assembly workflows.
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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: