Z-Pro-OH

98%

Reagent Code: #105559
label
Alias N-Benzyloxycarbonyl-L-Proline; N-Carbonylbenzyloxy-L-Purine, CBZ-L-Proline
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CAS Number 1148-11-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.26 g/mol
Formula C₁₃H₁₅NO₄
badge Registry Numbers
EC Number 214-557-4
MDL Number MFCD00003170
thermostat Physical Properties
Melting Point 75-77 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Z-Pro-OH is widely used in peptide synthesis as a protecting group for proline. It helps in the selective protection of the amino group during the formation of peptide bonds, ensuring the desired sequence is achieved without unwanted side reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it aids in the stepwise assembly of peptides. Additionally, it is employed in the preparation of peptide-based pharmaceuticals, where precise control over peptide structure is critical for biological activity. Its stability and compatibility with various coupling reagents make it a reliable choice in both research and industrial applications.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to almost white powder to crystal
Purity (%) 97.5-100%
Melting Point (°C) 76-78
Infrared Spectrum Conforms To Structure
Specific Rotation [a]20/D (c=2, EtOH) -42.0--38.0

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿280.00
inventory 25g
10-20 days ฿480.00
inventory 100g
10-20 days ฿1,420.00
inventory 500g
10-20 days ฿5,550.00
Z-Pro-OH
Z-Pro-OH is widely used in peptide synthesis as a protecting group for proline. It helps in the selective protection of the amino group during the formation of peptide bonds, ensuring the desired sequence is achieved without unwanted side reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it aids in the stepwise assembly of peptides. Additionally, it is employed in the preparation of peptide-based pharmaceuticals, where precise control over peptide structure is critical for biological activity. Its stability and compatibility with various coupling reagents make it a reliable choice in both research and industrial applications.
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