Fmoc-Asp(OMpe)-OH

97%

Reagent Code: #51167
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CAS Number 180675-08-5

science Other reagents with same CAS 180675-08-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 439.50 g/mol
Formula C₂₅H₂₉NO₆
badge Registry Numbers
MDL Number MFCD10001333
inventory_2 Storage & Handling
Storage -20°C, dry sealed

description Product Description

This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected form of aspartic acid, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group, and the OMpe (4-methoxyphenethyl) group protects the side chain carboxyl group. This protection strategy is crucial for ensuring selective reactions during the stepwise assembly of peptides, preventing unwanted side reactions. It is especially valuable in the synthesis of complex peptides and proteins, where precise control over the sequence and structure is required. Additionally, it finds applications in the development of pharmaceuticals, bioactive peptides, and research tools for studying protein function and interactions. Its stability and compatibility with SPPS make it a preferred choice in both academic and industrial settings.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿9,350.00
250mg
10-20 days ฿1,270.00
100mg
10-20 days ฿620.00
1g
10-20 days ฿3,020.00
Fmoc-Asp(OMpe)-OH
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This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected form of aspartic acid, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group, and the OMpe (4-methoxyphenethyl) group protects the side chain carboxyl group. This protection strategy is crucial for ensuring selective reactions during the stepwise assembly of peptides, preventing unwanted side reactions. It is especia

This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected form of aspartic acid, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group, and the OMpe (4-methoxyphenethyl) group protects the side chain carboxyl group. This protection strategy is crucial for ensuring selective reactions during the stepwise assembly of peptides, preventing unwanted side reactions. It is especially valuable in the synthesis of complex peptides and proteins, where precise control over the sequence and structure is required. Additionally, it finds applications in the development of pharmaceuticals, bioactive peptides, and research tools for studying protein function and interactions. Its stability and compatibility with SPPS make it a preferred choice in both academic and industrial settings.

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