Fmoc-L-Asp(tBu)-L-Ser[PSI(Me,Me)Pro]-OH

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Reagent Code: #104166
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CAS Number 955048-92-7

science Other reagents with same CAS 955048-92-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 538.59 g/mol
Formula C₂₉H₃₄N₂O₈
badge Registry Numbers
MDL Number MFCD18427351
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, enabling the sequential assembly of peptides with high precision. The Fmoc group provides temporary protection for the amino group during synthesis, while the tBu group protects the carboxylic acid side chain of aspartic acid. The inclusion of the pseudoproline dipeptide (Ser[PSI(Me,Me)Pro]) helps to reduce aggregation and improve solubility during the synthesis of challenging peptide sequences, such as those prone to secondary structure formation. This compound is especially valuable in the production of complex peptides for research in biochemistry, pharmaceuticals, and drug development, where controlled and efficient synthesis is critical.

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inventory 1g
10-20 days ฿4,104.00

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Fmoc-L-Asp(tBu)-L-Ser[PSI(Me,Me)Pro]-OH
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This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, enabling the sequential assembly of peptides with high precision. The Fmoc group provides temporary protection for the amino group during synthesis, while the tBu group protects the carboxylic acid side chain of aspartic acid. The inclusion of the pseudoproline dipeptide (Ser[PSI(Me,Me)Pro]) helps to reduce aggregation and improve solubility d

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, enabling the sequential assembly of peptides with high precision. The Fmoc group provides temporary protection for the amino group during synthesis, while the tBu group protects the carboxylic acid side chain of aspartic acid. The inclusion of the pseudoproline dipeptide (Ser[PSI(Me,Me)Pro]) helps to reduce aggregation and improve solubility during the synthesis of challenging peptide sequences, such as those prone to secondary structure formation. This compound is especially valuable in the production of complex peptides for research in biochemistry, pharmaceuticals, and drug development, where controlled and efficient synthesis is critical.

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