Z-Trp-Trp-OH

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Reagent Code: #121108
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CAS Number 57850-17-6

science Other reagents with same CAS 57850-17-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 524.57 g/mol
Formula C₃₀H₂₈N₄O₅
badge Registry Numbers
MDL Number MFCD00022760
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Z-Trp-Trp-OH is a protected dipeptide building block used in peptide synthesis to incorporate consecutive tryptophan (Trp-Trp) residues into larger peptide chains. The Z (benzyloxycarbonyl) protecting group on the N-terminal tryptophan enables selective coupling reactions while preventing unwanted side reactions at the amino terminus. It is commonly employed in both solid-phase and solution-phase peptide synthesis for the production of complex peptides, pharmaceuticals, and bioactive molecules where precise control over sequence and structure is essential. Additionally, it serves as a valuable tool in biochemical research to investigate tryptophan-rich peptide motifs, protein interactions, folding, and stability.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿945.00
inventory 5g
10-20 days ฿3,285.00
inventory 25g
10-20 days ฿11,430.00

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Z-Trp-Trp-OH
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Z-Trp-Trp-OH is a protected dipeptide building block used in peptide synthesis to incorporate consecutive tryptophan (Trp-Trp) residues into larger peptide chains. The Z (benzyloxycarbonyl) protecting group on the N-terminal tryptophan enables selective coupling reactions while preventing unwanted side reactions at the amino terminus. It is commonly employed in both solid-phase and solution-phase peptide synthesis for the production of complex peptides, pharmaceuticals, and bioactive molecules where prec

Z-Trp-Trp-OH is a protected dipeptide building block used in peptide synthesis to incorporate consecutive tryptophan (Trp-Trp) residues into larger peptide chains. The Z (benzyloxycarbonyl) protecting group on the N-terminal tryptophan enables selective coupling reactions while preventing unwanted side reactions at the amino terminus. It is commonly employed in both solid-phase and solution-phase peptide synthesis for the production of complex peptides, pharmaceuticals, and bioactive molecules where precise control over sequence and structure is essential. Additionally, it serves as a valuable tool in biochemical research to investigate tryptophan-rich peptide motifs, protein interactions, folding, and stability.

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