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Structure of 212651-47-3
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a stable, moisture-tolerant hydrate form and integrates seamlessly into peptide synthesis workflows. The C-terminal carboxyl group enables efficient coupling, while the fluorenylmethoxycarbonyl (Fmoc) moiety ensures high-yield deprotection under mild basic conditions.
2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)acetic acid hydrate serves as a stable, bench-ready carbamate protecting group for amino acids and peptides. It facilitates efficient N-terminal protection in solid-phase peptide synthesis, offering excellent solubility, minimal side reactions, and straightforward deprotection under mild basic conditions. Its robust fluorenylmethoxycarbonyl (Fmoc) backbone ensures high fidelity in sequence assembly and compatibility with diverse functional groups.
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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: