(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-dimethylbutanoic acid

≥95%

Reagent Code: #38018
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CAS Number 1172579-62-2

science Other reagents with same CAS 1172579-62-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 367.44 g/mol
Formula C₂₂H₂₅NO₄
badge Registry Numbers
MDL Number MFCD27952009
thermostat Physical Properties
Boiling Point 532.0±29.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in the field of peptide synthesis, where it serves as a protecting group for amino acids. Its structure, featuring the fluorenylmethoxycarbonyl (Fmoc) group, is particularly valuable in solid-phase peptide synthesis (SPPS). The Fmoc group protects the amino group during the coupling reactions, ensuring selective and controlled peptide chain elongation. It can be easily removed under mild basic conditions, making it highly compatible with a wide range of amino acids and peptide sequences. Additionally, its methyl and dimethylbutanoic acid components contribute to its stability and solubility, facilitating efficient synthesis processes. This compound is widely employed in the production of pharmaceuticals, bioactive peptides, and research applications in biochemistry and molecular biology.

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Test Parameter Specification
Appearance White to Off-White Powder or Crystals
Purity (%) 95.0-100
Mass Spectrum Conforms to Structure
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿40,500.00
inventory 100mg
10-20 days ฿3,087.00
inventory 250mg
10-20 days ฿4,635.00
inventory 1g
10-20 days ฿11,565.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-dimethylbutanoic acid
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This chemical is primarily used in the field of peptide synthesis, where it serves as a protecting group for amino acids. Its structure, featuring the fluorenylmethoxycarbonyl (Fmoc) group, is particularly valuable in solid-phase peptide synthesis (SPPS). The Fmoc group protects the amino group during the coupling reactions, ensuring selective and controlled peptide chain elongation. It can be easily removed under mild basic conditions, making it highly compatible with a wide range of amino acids and peptide sequences. Additionally, its methyl and dimethylbutanoic acid components contribute to its stability and solubility, facilitating efficient synthesis processes. This compound is widely employed in the production of pharmaceuticals, bioactive peptides, and research applications in biochemistry and molecular biology.
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