Nalpha-Fmoc-Nbeta-Octanoyl-2,3-diaminopropionic acid

95%

Reagent Code: #124553
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CAS Number 1423018-04-5

science Other reagents with same CAS 1423018-04-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 452.54 g/mol
Formula C₂₆H₃₂N₂O₅
badge Registry Numbers
MDL Number MFCD18427298
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used in peptide synthesis, particularly for solid-phase peptide synthesis (SPPS), where it serves as a building block for incorporating modified amino acids into peptide chains. The Fmoc group provides protection for the alpha-amino group, while the octanoyl group introduces a hydrophobic side chain, enabling the study of lipidated peptides or peptides with enhanced membrane interaction properties. It is valuable in research focused on peptide-based drug development, biomaterials, and studies of protein-protein interactions. The compound’s structure allows for the creation of peptides with tailored properties, such as improved stability or specific binding capabilities.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,600.00

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Nalpha-Fmoc-Nbeta-Octanoyl-2,3-diaminopropionic acid
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Used in peptide synthesis, particularly for solid-phase peptide synthesis (SPPS), where it serves as a building block for incorporating modified amino acids into peptide chains. The Fmoc group provides protection for the alpha-amino group, while the octanoyl group introduces a hydrophobic side chain, enabling the study of lipidated peptides or peptides with enhanced membrane interaction properties. It is valuable in research focused on peptide-based drug development, biomaterials, and studies of protein-

Used in peptide synthesis, particularly for solid-phase peptide synthesis (SPPS), where it serves as a building block for incorporating modified amino acids into peptide chains. The Fmoc group provides protection for the alpha-amino group, while the octanoyl group introduces a hydrophobic side chain, enabling the study of lipidated peptides or peptides with enhanced membrane interaction properties. It is valuable in research focused on peptide-based drug development, biomaterials, and studies of protein-protein interactions. The compound’s structure allows for the creation of peptides with tailored properties, such as improved stability or specific binding capabilities.

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