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*For research and further manufacturing use only, not for direct human use.
Structure of 193885-59-5
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)decanoic acid is a chiral, bench-stable amino acid derivative featuring a bulky fluorenylmethoxycarbonyl (Fmoc) protecting group. This robust N-terminal block facilitates efficient peptide synthesis, enabling high-yield coupling and clean deprotection under mild conditions. The extended aliphatic side chain enhances solubility in organic solvents, streamlining purification workflows.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)decanoic acid serves as a robust, bench-stable amino acid derivative for solid-phase peptide synthesis. The Fmoc group enables efficient deprotection under mild basic conditions, while the aliphatic side chain provides compatibility with diverse coupling protocols. Its well-established reactivity and ease of purification make it a practical choice for constructing complex peptide scaffolds and functionalized building blocks in medicinal chemistry 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-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: