(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)butanoic acid

98%

Reagent Code: #37756
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CAS Number 201864-71-3

science Other reagents with same CAS 201864-71-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.36 g/mol
Formula C₁₉H₁₉NO₄
badge Registry Numbers
MDL Number MFCD00270344
thermostat Physical Properties
Boiling Point 555.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group during the synthesis process, preventing unwanted reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise addition of amino acids to build peptides with high precision. The Fmoc group can be easily removed under mild basic conditions, enabling the deprotection of the amino group without affecting the rest of the peptide chain. This makes it a crucial reagent in the production of peptides for research, pharmaceuticals, and biotechnology applications.

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Test Parameter Specification
Appearance White to Off-White Powder
Purity (%) 97.5-100%
Enantiomeric Excess (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿6,282.00
inventory 5g
10-20 days ฿3,618.00
inventory 1g
10-20 days ฿1,116.00

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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)butanoic acid
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This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group during the synthesis process, preventing unwanted reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise addition of amino acids to build peptides with high precision. The Fmoc group can be easily removed under mild basic conditions, enabling the deprotection of the amino group without affecting the rest of the peptide chain. This makes it a crucial reagent in the production of peptides for research, pharmaceuticals, and biotechnology applications.
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