Z-Glu(OtBu)-OH

99.0%

Reagent Code: #105668
label
Alias N-Benzyloxycarbonyl-L-glutamic acid γ-tert-butyl ester; N-carbonylbenzyloxy-L-glutamic acid 5-tert-butyl ether
fingerprint
CAS Number 3886-08-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 337.37 g/mol
Formula C₁₇H₂₃NO₆
badge Registry Numbers
EC Number 223-421-3
MDL Number MFCD00038274
thermostat Physical Properties
Melting Point 83-87 °C
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Z-Glu(OtBu)-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected form of glutamic acid, where the tert-butyl ester group protects the carboxyl side chain, preventing unwanted reactions during peptide chain assembly. This protection allows for selective deprotection and activation of specific functional groups, enabling the precise construction of complex peptides. It is especially valuable in synthesizing peptides with glutamic acid residues, ensuring the integrity of the side chain functionality. Additionally, it is employed in the development of peptide-based pharmaceuticals, bioactive peptides, and research tools for studying protein interactions and enzymatic processes. Its stability and compatibility with various coupling reagents make it a reliable building block in organic and medicinal chemistry.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to almost white powder to crystal
Purity (%) 98.5-100%
Specific Rotation [α]20/D (C=2, MeOH) -10 to 15
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days $258.23
inventory 1g
10-20 days $12.50
inventory 5g
10-20 days $16.81
inventory 25g
10-20 days $75.44
Z-Glu(OtBu)-OH
Z-Glu(OtBu)-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected form of glutamic acid, where the tert-butyl ester group protects the carboxyl side chain, preventing unwanted reactions during peptide chain assembly. This protection allows for selective deprotection and activation of specific functional groups, enabling the precise construction of complex peptides. It is especially valuable in synthesizing peptides with glutamic acid residues, ensuring the integrity of the side chain functionality. Additionally, it is employed in the development of peptide-based pharmaceuticals, bioactive peptides, and research tools for studying protein interactions and enzymatic processes. Its stability and compatibility with various coupling reagents make it a reliable building block in organic and medicinal chemistry.
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