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Structure of 166410-28-2
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Fmoc-t-Bu-EDC delivers a robust, moisture-tolerant protecting group for amine-directed coupling in peptide synthesis. This stable, bench-ready derivative integrates seamlessly into automated workflows, enabling efficient chain elongation without side reactions.
(9H-Fluoren-9-yl)methyl tert-butyl ethane-1,2-diyldicarbamate serves as a robust, bench-stable dipeptide protecting group reagent, enabling efficient N-terminal protection in solid-phase and solution-phase peptide synthesis. Its orthogonal cleavage profile facilitates selective deprotection under mild acidic conditions, while the fluorenylmethoxy carbonyl (Fmoc) moiety ensures high coupling efficiency and minimal epimerization. The tert-butyl ethane-1,2-diyldicarbamate linker enhances stability during purification and reaction workup, making it ideal for complex peptide assembly and fragment coupling 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: