Z-Tyr-OH
98%
Reagent
Code: #105673
Alias
N-Benzyloxycarbonyl-L-tyrosine ; CBZ-L-tyrosine
CAS Number
1164-16-5
blur_circular Chemical Specifications
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Molecular Information
Weight
315.32 g/mol
Formula
C₁₇H₁₇NO₅
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Registry Numbers
EC Number
214-609-6
MDL Number
MFCD00191899
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Physical Properties
Melting Point
57-60 °C(lit.)
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Storage & Handling
Storage
Room temperature, dry, sealed
description Product Description
Z-Tyr-OH is widely used in peptide synthesis as a protecting group for tyrosine. It helps in preventing unwanted side reactions during the formation of peptide bonds, ensuring the integrity and specificity of the final peptide product. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it aids in the stepwise assembly of amino acids. Additionally, Z-Tyr-OH is employed in the development of bioactive peptides and pharmaceutical compounds, where precise control over amino acid reactivity is crucial. Its application extends to research in biochemistry and molecular biology, where it is used to study protein interactions and enzyme mechanisms.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Melting Point | 93-97 |
Purity (HPLC) | 98-100% |
Purity (Neutralization Titration) | 97.5-102.5% |
Specific Rotation [a]20/d(c=1%, Acetic Acid) | |
Specific Rotation [A]20/D (C=1%, Acetic Acid) | 8-12 |
Appearance | Colorless Liquid |
Infrared Spectrum | Conforms to Structure |
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Z-Tyr-OH
Z-Tyr-OH is widely used in peptide synthesis as a protecting group for tyrosine. It helps in preventing unwanted side reactions during the formation of peptide bonds, ensuring the integrity and specificity of the final peptide product. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it aids in the stepwise assembly of amino acids. Additionally, Z-Tyr-OH is employed in the development of bioactive peptides and pharmaceutical compounds, where precise control over amino acid reactivity is crucial. Its application extends to research in biochemistry and molecular biology, where it is used to study protein interactions and enzyme mechanisms.
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