Boc-Orn(Z)-Osu

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Reagent Code: #104830
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CAS Number 57225-25-9

science Other reagents with same CAS 57225-25-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 463.48 g/mol
Formula C₂₂H₂₉N₃O₈
badge Registry Numbers
MDL Number MFCD00236870
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Boc-Orn(Z)-OSu is a protected and activated form of ornithine, specifically Nα-Boc-Nδ-Z-ornithine N-hydroxysuccinimide ester. It is widely used in peptide synthesis to incorporate the ornithine residue into peptide chains. The Boc (tert-butyloxycarbonyl) group protects the α-amino group, the Z (benzyloxycarbonyl) group protects the δ-amino group on the side chain, and the OSu active ester enables efficient and racemization-free coupling to the N-terminus of growing peptides. This reagent is essential in both solid-phase and solution-phase peptide synthesis, supporting the precise construction of complex peptide sequences for pharmaceutical research, bioactive peptide development, and biochemical studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,650.00

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Boc-Orn(Z)-Osu
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Boc-Orn(Z)-OSu is a protected and activated form of ornithine, specifically Nα-Boc-Nδ-Z-ornithine N-hydroxysuccinimide ester. It is widely used in peptide synthesis to incorporate the ornithine residue into peptide chains. The Boc (tert-butyloxycarbonyl) group protects the α-amino group, the Z (benzyloxycarbonyl) group protects the δ-amino group on the side chain, and the OSu active ester enables efficient and racemization-free coupling to the N-terminus of g

Boc-Orn(Z)-OSu is a protected and activated form of ornithine, specifically Nα-Boc-Nδ-Z-ornithine N-hydroxysuccinimide ester. It is widely used in peptide synthesis to incorporate the ornithine residue into peptide chains. The Boc (tert-butyloxycarbonyl) group protects the α-amino group, the Z (benzyloxycarbonyl) group protects the δ-amino group on the side chain, and the OSu active ester enables efficient and racemization-free coupling to the N-terminus of growing peptides. This reagent is essential in both solid-phase and solution-phase peptide synthesis, supporting the precise construction of complex peptide sequences for pharmaceutical research, bioactive peptide development, and biochemical studies.

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