Fmoc-N-Me-Abu(4)-OH

95%

Reagent Code: #105131
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CAS Number 221124-57-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 339.39 g/mol
Formula C₂₀H₂₁NO₄
badge Registry Numbers
MDL Number MFCD08275875
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality, allowing for selective deprotection during the synthesis process. The N-Me (N-methyl) modification enhances the stability and can influence the conformational properties of the resulting peptide. The Abu (2-aminobutyric acid) moiety, with its specific side chain, is incorporated into peptides to study structure-activity relationships or to modify peptide properties such as hydrophobicity, flexibility, or resistance to enzymatic degradation. This chemical is especially valuable in the development of bioactive peptides, peptidomimetics, and pharmaceutical compounds where precise control over amino acid incorporation is critical.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,681.00
inventory 250mg
10-20 days ฿1,368.00
inventory 5g
10-20 days ฿12,861.00
Fmoc-N-Me-Abu(4)-OH
This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality, allowing for selective deprotection during the synthesis process. The N-Me (N-methyl) modification enhances the stability and can influence the conformational properties of the resulting peptide. The Abu (2-aminobutyric acid) moiety, with its specific side chain, is incorporated into peptides to study structure-activity relationships or to modify peptide properties such as hydrophobicity, flexibility, or resistance to enzymatic degradation. This chemical is especially valuable in the development of bioactive peptides, peptidomimetics, and pharmaceutical compounds where precise control over amino acid incorporation is critical.
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