BOC-ARG(Z)-OH

98%

Reagent Code: #66137
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CAS Number 51219-18-2

science Other reagents with same CAS 51219-18-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 408.45 g/mol
Formula C₁₉H₂₈N₄O₆
badge Registry Numbers
MDL Number MFCD00058482
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

BOC-ARG(Z)-OH is widely used in peptide synthesis as a protecting group for the amino acid arginine. The BOC (tert-butyloxycarbonyl) group protects the amine functionality, while the Z (benzyloxycarbonyl) group safeguards the guanidine side chain of arginine. This dual protection ensures selective reactions during peptide chain assembly, particularly in solid-phase peptide synthesis (SPPS). It is essential in synthesizing complex peptides and proteins, where precise control over amino acid reactivity is critical. Additionally, it finds applications in the development of pharmaceuticals, including peptide-based drugs, and in biochemical research for studying protein interactions and functions. Its stability under various reaction conditions makes it a valuable reagent in organic and medicinal chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,071.00
1g
10-20 days ฿2,556.00
5g
10-20 days ฿8,928.00
BOC-ARG(Z)-OH
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BOC-ARG(Z)-OH is widely used in peptide synthesis as a protecting group for the amino acid arginine. The BOC (tert-butyloxycarbonyl) group protects the amine functionality, while the Z (benzyloxycarbonyl) group safeguards the guanidine side chain of arginine. This dual protection ensures selective reactions during peptide chain assembly, particularly in solid-phase peptide synthesis (SPPS). It is essential in synthesizing complex peptides and proteins, where precise control over amino acid reactivity is

BOC-ARG(Z)-OH is widely used in peptide synthesis as a protecting group for the amino acid arginine. The BOC (tert-butyloxycarbonyl) group protects the amine functionality, while the Z (benzyloxycarbonyl) group safeguards the guanidine side chain of arginine. This dual protection ensures selective reactions during peptide chain assembly, particularly in solid-phase peptide synthesis (SPPS). It is essential in synthesizing complex peptides and proteins, where precise control over amino acid reactivity is critical. Additionally, it finds applications in the development of pharmaceuticals, including peptide-based drugs, and in biochemical research for studying protein interactions and functions. Its stability under various reaction conditions makes it a valuable reagent in organic and medicinal chemistry.

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