Fmoc-Arg(Pbf)-OH
98%
Reagent
Code: #105144
Alias
Fmoc-Pbf-Arginine ; N-Fremoxycarbonyl-2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-L-arginine
CAS Number
154445-77-9
blur_circular Chemical Specifications
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Molecular Information
Weight
648.77 g/mol
Formula
C₃₄H₄₀N₄O₇S
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Registry Numbers
MDL Number
MFCD00235804
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Physical Properties
Melting Point
132°C
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Storage & Handling
Storage
-20°C
description Product Description
Fmoc-Arg(Pbf)-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected form of arginine, where the Fmoc group safeguards the amino group, and the Pbf group protects the guanidine side chain. This protection is crucial to prevent unwanted reactions during the stepwise assembly of peptides. Its application is essential in producing complex peptides with high purity, as it allows for selective deprotection and coupling at specific stages of synthesis. This chemical is particularly valuable in the development of pharmaceuticals, bioactive peptides, and research tools in biochemistry and molecular biology. Its stability and compatibility with SPPS protocols make it a preferred choice for synthesizing arginine-containing peptides.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (HPLC) | 98-100 |
Specific Gravity (20/20 Degree Celsius) | 4-7 |
Appearance | Colorless or white powder or crystals |
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Fmoc-Arg(Pbf)-OH
Fmoc-Arg(Pbf)-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected form of arginine, where the Fmoc group safeguards the amino group, and the Pbf group protects the guanidine side chain. This protection is crucial to prevent unwanted reactions during the stepwise assembly of peptides. Its application is essential in producing complex peptides with high purity, as it allows for selective deprotection and coupling at specific stages of synthesis. This chemical is particularly valuable in the development of pharmaceuticals, bioactive peptides, and research tools in biochemistry and molecular biology. Its stability and compatibility with SPPS protocols make it a preferred choice for synthesizing arginine-containing peptides.
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