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Structure of 200335-40-6
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Fmoc-Asp-NH2 is a protected aspartic acid derivative featuring a fluorenylmethoxycarbonyl group at the α-amino terminus and a free carboxylic acid at the side chain. This configuration enables direct incorporation into solid-phase peptide synthesis workflows, where the side-chain protection remains stable under standard deprotection conditions. The Fmoc moiety facilitates efficient coupling and selective removal via mild base treatment, streamlining sequence assembly.
Fmoc-Asp-NH2 serves as a key building block in solid-phase peptide synthesis, offering orthogonal protection for both the α-amino and side-chain carboxyl groups. The Fmoc group enables mild base-labile deprotection, while the side-chain is protected as a stable tert-butyl ester, facilitating selective functionalization. Its bench-stable, crystalline form simplifies handling and purification, making it ideal for synthesizing complex peptides, including those containing acidic residues or requiring precise sequence control.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: