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*For research and further manufacturing use only, not for direct human use.
Structure of 288149-55-3
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Fmoc-Glu-NH2 delivers a protected glutamic acid derivative with enhanced solubility and stability in aqueous and organic solvents. The fluorenylmethyloxycarbonyl (Fmoc) group enables efficient, orthogonal coupling in solid-phase peptide synthesis, while the free α-amino and side-chain carboxylate functionalities allow precise incorporation into bioactive sequences. This derivative supports robust yield and minimal racemization during chain elongation.
Fmoc-Glu-NH₂ serves as a key building block in solid-phase peptide synthesis, enabling efficient incorporation of glutamic acid residues with side-chain protection. The Fmoc group ensures orthogonal deprotection under mild basic conditions, while the α-amino and side-chain carboxyl functionalities facilitate standard coupling reactions. Its bench-stable, crystalline nature supports reliable handling and purification, making it ideal for synthesizing bioactive peptides and protein conjugates.
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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: