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Structure of 174879-28-8
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a robust C-terminal carbamate group, enabling efficient coupling in solid-phase peptide synthesis. The fluoren-9-ylmethoxy carbonyl (Fmoc) moiety provides excellent orthogonal protection and facilitates mild deprotection under basic conditions. This bench-stable compound integrates seamlessly into complex peptide sequences with high fidelity.
2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)butanoic acid serves as a robust amino acid derivative for peptide synthesis, offering excellent solubility and stability under standard coupling conditions. The Fmoc group enables efficient, orthogonal protection of the amine, facilitating selective deprotection during iterative chain elongation. Its well-documented compatibility with common coupling reagents and ease of purification make it a practical choice for solid-phase and solution-phase 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: