Fmoc-Dap(Alloc)-OH

≥98.5% (HPLC)

Reagent Code: #96093
label
Alias Nβ-Alloc-Nα-Fmoc-L-2,3-diaminopropionic acid Nβ-allyloxycarbonyl-Nα-Fmoc-L-2,3-diaminopropionic acid N-fluorenylmethoxycarbonyl-3-[ [(allyloxy)carbonyl]amino]-L-alanine
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CAS Number 188970-92-5

science Other reagents with same CAS 188970-92-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 410.42 g/mol
Formula C₂₂H₂₂N₂O₆
badge Registry Numbers
MDL Number MFCD00273468
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc group protects the amino group during the synthesis process, while the Alloc group protects the side chain. This dual protection allows for selective deprotection, enabling the synthesis of complex peptides with high precision. It is especially valuable in the production of peptides with specific sequences or modifications, such as those used in pharmaceutical research, drug development, and biochemical studies. Its application ensures efficient and controlled peptide chain assembly, making it a critical component in the synthesis of therapeutic peptides and peptidomimetics.

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Test Parameter Specification
Purity (HPLC) 98.5-100%
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,134.00
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Fmoc-Dap(Alloc)-OH
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This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc group protects the amino group during the synthesis process, while the Alloc group protects the side chain. This dual protection allows for selective deprotection, enabling the synthesis of complex peptides with high precision. It is especially valuable in the production of peptides with specific sequences or modifications, such as those used in pharmaceutical research, drug development, and biochemical studies. Its application ensures efficient and controlled peptide chain assembly, making it a critical component in the synthesis of therapeutic peptides and peptidomimetics.
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