Z-Trp-OH

98%

Reagent Code: #105669
label
Alias N-Benzyloxycarbonyl-L-Tryptophan; Z-Tryptophan, CBZ-L-Tryptophan
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CAS Number 7432-21-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 338.36 g/mol
Formula C₁₉H₁₈N₂O₄
badge Registry Numbers
EC Number 231-074-4
MDL Number MFCD00065700
thermostat Physical Properties
Melting Point 124-127 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Z-Trp-OH is widely used in peptide synthesis as a protecting group for the amino acid tryptophan. It helps in preventing unwanted side reactions during the formation of peptide bonds, ensuring the integrity of the peptide chain. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where selective protection and deprotection of amino acids are crucial. Additionally, Z-Trp-OH is employed in the development of bioactive peptides and pharmaceuticals, where precise control over peptide structure is essential for achieving desired biological activity. Its stability and compatibility with various coupling reagents make it a reliable choice for researchers in the field of peptide chemistry.

format_list_bulleted Product Specification

Test Parameter Specification
Enantiomeric Excess 98
Melting Point 123-127
Purity (HPLC) 98-100%
Specific Rotation [A]20/D (C=3, Acetic Acid) 2.7-3.5
ACETICACID
Appearance White to Light Yellow Powder
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿1,230.00
Z-Trp-OH
Z-Trp-OH is widely used in peptide synthesis as a protecting group for the amino acid tryptophan. It helps in preventing unwanted side reactions during the formation of peptide bonds, ensuring the integrity of the peptide chain. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where selective protection and deprotection of amino acids are crucial. Additionally, Z-Trp-OH is employed in the development of bioactive peptides and pharmaceuticals, where precise control over peptide structure is essential for achieving desired biological activity. Its stability and compatibility with various coupling reagents make it a reliable choice for researchers in the field of peptide chemistry.
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