Fmoc-D-Arg(Pbf)-OH

98%

Reagent Code: #76582
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CAS Number 187618-60-0

science Other reagents with same CAS 187618-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 648.8 g/mol
Formula C₃₄H₄₀N₄O₇S
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for introducing D-arginine residues into peptide sequences. The Fmoc (fluorenylmethyloxycarbonyl) group acts as a protecting group for the amino group, ensuring selective reactions during peptide chain assembly. The Pbf (2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl) group protects the guanidine side chain of arginine, preventing unwanted side reactions. Its application is crucial in the production of peptides for research, pharmaceuticals, and biotechnology, where precise sequence control is essential. It is particularly valuable in synthesizing peptides with D-amino acids, which are often used to enhance stability and bioavailability in therapeutic peptides.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,521.00
5g
10-20 days ฿6,084.00
Fmoc-D-Arg(Pbf)-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 building block for introducing D-arginine residues into peptide sequences. The Fmoc (fluorenylmethyloxycarbonyl) group acts as a protecting group for the amino group, ensuring selective reactions during peptide chain assembly. The Pbf (2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl) group protects the guanidine side chain of arginine, preventing unwanted side reactions. Its a

This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for introducing D-arginine residues into peptide sequences. The Fmoc (fluorenylmethyloxycarbonyl) group acts as a protecting group for the amino group, ensuring selective reactions during peptide chain assembly. The Pbf (2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl) group protects the guanidine side chain of arginine, preventing unwanted side reactions. Its application is crucial in the production of peptides for research, pharmaceuticals, and biotechnology, where precise sequence control is essential. It is particularly valuable in synthesizing peptides with D-amino acids, which are often used to enhance stability and bioavailability in therapeutic peptides.

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