Boc-D-Dap(Fmoc)-OH

95%

Reagent Code: #144632
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CAS Number 131570-56-4

science Other reagents with same CAS 131570-56-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 426.46 g/mol
Formula C₂₃H₂₆N₂O₆
badge Registry Numbers
MDL Number MFCD00236844
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used in solid-phase peptide synthesis as a protected amino acid building block. The Boc and Fmoc groups provide orthogonal protection for the alpha-amino and side-chain amino functions, respectively, allowing selective deprotection during stepwise peptide assembly. Particularly useful for incorporating D-configured diaminopropionic acid into peptide sequences where stereochemistry and side-chain functionality are critical, such as in the development of peptide-based drugs, enzyme inhibitors, or bioactive probes. Its protected form ensures minimal side reactions and high coupling efficiency in automated synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿335.50
inventory 5g
10-20 days ฿918.50
inventory 25g
10-20 days ฿8,060.00
inventory 100g
10-20 days ฿32,170.00
inventory 250mg
10-20 days ฿148.50

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Boc-D-Dap(Fmoc)-OH
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Used in solid-phase peptide synthesis as a protected amino acid building block. The Boc and Fmoc groups provide orthogonal protection for the alpha-amino and side-chain amino functions, respectively, allowing selective deprotection during stepwise peptide assembly. Particularly useful for incorporating D-configured diaminopropionic acid into peptide sequences where stereochemistry and side-chain functionality are critical, such as in the development of peptide-based drugs, enzyme inhibitors, or bioactive

Used in solid-phase peptide synthesis as a protected amino acid building block. The Boc and Fmoc groups provide orthogonal protection for the alpha-amino and side-chain amino functions, respectively, allowing selective deprotection during stepwise peptide assembly. Particularly useful for incorporating D-configured diaminopropionic acid into peptide sequences where stereochemistry and side-chain functionality are critical, such as in the development of peptide-based drugs, enzyme inhibitors, or bioactive probes. Its protected form ensures minimal side reactions and high coupling efficiency in automated synthesis.

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