Z-D-Dbu(Boc)-OH

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Reagent Code: #246765
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CAS Number 96186-30-0

science Other reagents with same CAS 96186-30-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 352.382 g/mol
Formula C₁₇H₂₄N₂O₆
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in peptide synthesis as a protected amino acid derivative, particularly in the preparation of complex peptides where selective deprotection and coupling are required. The Boc (tert-butoxycarbonyl) group provides temporary protection of the amine functionality, allowing controlled stepwise assembly of peptide chains. The Z (benzyloxycarbonyl) group offers orthogonal protection that can be removed independently under mild conditions, enabling precise manipulation in multi-step syntheses. Commonly employed in solid-phase and solution-phase peptide synthesis, especially in the production of pharmaceutical intermediates and bioactive peptides. Its stability under various reaction conditions makes it suitable for use in automated peptide synthesizers.

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inventory 1g
10-20 days ฿17,990.00

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Z-D-Dbu(Boc)-OH
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Used in peptide synthesis as a protected amino acid derivative, particularly in the preparation of complex peptides where selective deprotection and coupling are required. The Boc (tert-butoxycarbonyl) group provides temporary protection of the amine functionality, allowing controlled stepwise assembly of peptide chains. The Z (benzyloxycarbonyl) group offers orthogonal protection that can be removed independently under mild conditions, enabling precise manipulation in multi-step syntheses. Commonly empl

Used in peptide synthesis as a protected amino acid derivative, particularly in the preparation of complex peptides where selective deprotection and coupling are required. The Boc (tert-butoxycarbonyl) group provides temporary protection of the amine functionality, allowing controlled stepwise assembly of peptide chains. The Z (benzyloxycarbonyl) group offers orthogonal protection that can be removed independently under mild conditions, enabling precise manipulation in multi-step syntheses. Commonly employed in solid-phase and solution-phase peptide synthesis, especially in the production of pharmaceutical intermediates and bioactive peptides. Its stability under various reaction conditions makes it suitable for use in automated peptide synthesizers.

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