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Structure of 2413365-23-6
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This fluorenylmethoxycarbonyl-protected lysine derivative enables efficient solid-phase peptide synthesis, featuring a tert-butyl ester that facilitates selective deprotection under mild acidic conditions. The fluoren-9-ylmethoxycarbonyl (Fmoc) group ensures high coupling efficiency and stability during chain elongation, while the hydrochloride salt enhances solubility in common organic solvents.
tert-Butyl (((9H-fluoren-9-yl)methoxy)carbonyl)-L-lysinate hydrochloride serves as a robust, bench-stable amino acid derivative enabling efficient N-terminal protection in peptide synthesis. The Fmoc group facilitates orthogonal deprotection under mild basic conditions, while the tert-butyl ester permits selective side-chain modulation. This reagent exhibits excellent solubility and functional group tolerance, streamlining sequence assembly in solid-phase and solution-phase 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: