Z-Glu(OtBu)-OH
99.0%
Reagent
Code: #105668
Alias
N-Benzyloxycarbonyl-L-glutamic acid γ-tert-butyl ester; N-carbonylbenzyloxy-L-glutamic acid 5-tert-butyl ether
CAS Number
3886-08-6
blur_circular Chemical Specifications
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Molecular Information
Weight
337.37 g/mol
Formula
C₁₇H₂₃NO₆
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Registry Numbers
EC Number
223-421-3
MDL Number
MFCD00038274
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Physical Properties
Melting Point
83-87 °C
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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 |
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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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