Z-Asp(OMe)-OH

98.0%

Reagent Code: #105663
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CAS Number 3160-47-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.26 g/mol
Formula C₁₃H₁₅NO₆
badge Registry Numbers
MDL Number MFCD00133585
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Z-Asp(OMe)-OH is widely used in peptide synthesis as a protected form of aspartic acid. Its primary application is in the construction of peptides where aspartic acid needs to be incorporated without unwanted side reactions. The methoxy (OMe) group protects the carboxylic acid functionality, ensuring selective reactions at other sites during peptide chain elongation. This compound is particularly valuable in solid-phase peptide synthesis (SPPS) and solution-phase methods, where protecting groups are essential for controlling the sequence and integrity of the peptide. Additionally, it is utilized in the development of pharmaceuticals and bioactive peptides, where precise amino acid incorporation is critical for maintaining the desired biological activity. Its stability and ease of deprotection make it a reliable choice for researchers and industrial applications in peptide chemistry.

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Test Parameter Specification
Purity (HPLC) 98-100
Infrared Spectrometry Conforms To Structure
Proton NMR Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,548.00
inventory 25g
10-20 days ฿5,724.00
Z-Asp(OMe)-OH
Z-Asp(OMe)-OH is widely used in peptide synthesis as a protected form of aspartic acid. Its primary application is in the construction of peptides where aspartic acid needs to be incorporated without unwanted side reactions. The methoxy (OMe) group protects the carboxylic acid functionality, ensuring selective reactions at other sites during peptide chain elongation. This compound is particularly valuable in solid-phase peptide synthesis (SPPS) and solution-phase methods, where protecting groups are essential for controlling the sequence and integrity of the peptide. Additionally, it is utilized in the development of pharmaceuticals and bioactive peptides, where precise amino acid incorporation is critical for maintaining the desired biological activity. Its stability and ease of deprotection make it a reliable choice for researchers and industrial applications in peptide chemistry.
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