Fmoc-Pro-OH

98%

Reagent Code: #105103
label
Alias Fmoc-L-proline ; N-tert-butylfluorenylmethoxycarbonyl-L-proline
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CAS Number 71989-31-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 337.37 g/mol
Formula C₂₀H₁₉NO₄
badge Registry Numbers
EC Number 276-259-0
MDL Number MFCD00037122
thermostat Physical Properties
Melting Point 117-118 °C(lit.)
inventory_2 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.

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Test Parameter Specification
Purity (HPLC) 98
Melting Point 114-119
Purity (Neutralization Titration) 98-100
Specific Rotation (20 °C) -35--31

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿320.00
inventory 100g
10-20 days ฿2,980.00
inventory 25g
10-20 days ฿960.00
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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