Fmoc-norArg(Pbf)-OH

97%

Reagent Code: #52359
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CAS Number 1313054-32-8

science Other reagents with same CAS 1313054-32-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 634.74 g/mol
Formula C₃₃H₃₈N₄O₇S
badge Registry Numbers
MDL Number MFCD15142017
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amine functionality, and the Pbf (2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl) group protects the guanidine side chain of norarginine. This protection is crucial to prevent unwanted side reactions during the peptide assembly process. It is widely employed in the production of peptides for research, pharmaceuticals, and biotechnology applications, enabling the precise construction of peptide chains with specific sequences. Its stability and compatibility with SPPS make it a valuable tool for synthesizing complex peptides and proteins.

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Test Parameter Specification
Appearance White Powder
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,517.00
inventory 100mg
10-20 days ฿2,763.00

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Fmoc-norArg(Pbf)-OH
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This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amine functionality, and the Pbf (2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl) group protects the guanidine side chain of norarginine. This protection is crucial to prevent unwanted side reactions during the peptide assembly process. It is widely employed in the production of peptide

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amine functionality, and the Pbf (2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl) group protects the guanidine side chain of norarginine. This protection is crucial to prevent unwanted side reactions during the peptide assembly process. It is widely employed in the production of peptides for research, pharmaceuticals, and biotechnology applications, enabling the precise construction of peptide chains with specific sequences. Its stability and compatibility with SPPS make it a valuable tool for synthesizing complex peptides and proteins.

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