Fmoc-Pro-OH
98%
Reagent
Code: #105103
Alias
Fmoc-L-proline ; N-tert-butylfluorenylmethoxycarbonyl-L-proline
CAS Number
71989-31-6
blur_circular Chemical Specifications
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Molecular Information
Weight
337.37 g/mol
Formula
C₂₀H₁₉NO₄
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Registry Numbers
EC Number
276-259-0
MDL Number
MFCD00037122
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Physical Properties
Melting Point
117-118 °C(lit.)
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Storage & Handling
Storage
room temperature
description Product Description
Fmoc-Pro-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a key building block for introducing proline residues into peptide chains. The Fmoc (fluorenylmethyloxycarbonyl) group acts as a protective group for the amino group, allowing for selective deprotection and coupling during the synthesis process. This compound is essential in the production of peptides for pharmaceutical research, drug development, and biochemical studies. Its stability and compatibility with SPPS protocols make it a valuable reagent for creating peptides with specific sequences and functions. Additionally, it is utilized in the synthesis of peptidomimetics and other biologically active compounds.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (HPLC) | 98 |
Melting Point | 114-119 |
Purity (Neutralization Titration) | 98-100 |
Specific Rotation (20 °C) | -35--31 |
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Fmoc-Pro-OH
Fmoc-Pro-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a key building block for introducing proline residues into peptide chains. The Fmoc (fluorenylmethyloxycarbonyl) group acts as a protective group for the amino group, allowing for selective deprotection and coupling during the synthesis process. This compound is essential in the production of peptides for pharmaceutical research, drug development, and biochemical studies. Its stability and compatibility with SPPS protocols make it a valuable reagent for creating peptides with specific sequences and functions. Additionally, it is utilized in the synthesis of peptidomimetics and other biologically active compounds.
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