Fmoc-Ala-Thr(Psi(Me,Me)pro)-OH

≥95%

Reagent Code: #37008
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CAS Number 252554-79-3

science Other reagents with same CAS 252554-79-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 452.50 g/mol
Formula C₂₅H₂₈N₂O₆
badge Registry Numbers
MDL Number MFCD03490490
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for constructing peptides with specific structural features, leveraging the Fmoc (fluorenylmethyloxycarbonyl) protecting group for temporary protection of the amino group during synthesis. The inclusion of the pseudoproline dipeptide (Psi(Me,Me)pro) enhances the solubility and reduces aggregation of peptide chains, which is especially beneficial for synthesizing long or complex peptides. This compound is valuable in research and development of therapeutic peptides, as it helps improve the efficiency and yield of peptide synthesis processes.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿14,049.00
inventory 1g
10-20 days ฿6,174.00
inventory 250mg
10-20 days ฿3,087.00

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Fmoc-Ala-Thr(Psi(Me,Me)pro)-OH
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This chemical is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for constructing peptides with specific structural features, leveraging the Fmoc (fluorenylmethyloxycarbonyl) protecting group for temporary protection of the amino group during synthesis. The inclusion of the pseudoproline dipeptide (Psi(Me,Me)pro) enhances the solubility and reduces aggregation of peptide chains, which is especially beneficial for synthesizing l
This chemical is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for constructing peptides with specific structural features, leveraging the Fmoc (fluorenylmethyloxycarbonyl) protecting group for temporary protection of the amino group during synthesis. The inclusion of the pseudoproline dipeptide (Psi(Me,Me)pro) enhances the solubility and reduces aggregation of peptide chains, which is especially beneficial for synthesizing long or complex peptides. This compound is valuable in research and development of therapeutic peptides, as it helps improve the efficiency and yield of peptide synthesis processes.
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