Fmoc chloride

For HPLC derivatization, ≥99.0% (HPLC)

Reagent Code: #93705
label
Alias Fluorenylmethyloxycarbonyl chloride; 9-fluorenylmethyl chloroformate, 9-fluorenylmethyloxycarbonyl chloride, 9-fluorenylmethyl chloroformate
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CAS Number 28920-43-6

science Other reagents with same CAS 28920-43-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.7 g/mol
Formula C₁₅H₁₁ClO₂
badge Registry Numbers
EC Number 249-313-6
MDL Number MFCD00001138
thermostat Physical Properties
Melting Point 62-64 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Fmoc chloride is widely used in peptide synthesis as a protecting group for amino acids. It reacts with the amino group to form an Fmoc-protected amino acid, which prevents unwanted side reactions during peptide chain assembly. This protection is crucial in solid-phase peptide synthesis (SPPS), where the Fmoc group can be easily removed under mild basic conditions, allowing for sequential addition of amino acids. Its stability and selective deprotection make it a preferred choice in the production of complex peptides and proteins for pharmaceutical and biochemical research. Additionally, Fmoc chloride is employed in the synthesis of other organic compounds where temporary protection of amine groups is required.

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Test Parameter Specification
Melting point 60-65
Purity (HPLC) 99-100%
Appearance White to yellow powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,120.00
inventory 1g
10-20 days ฿4,100.00
inventory 25g
10-20 days ฿32,800.00
inventory 5g
10-20 days ฿11,600.00
inventory 100g
10-20 days ฿82,000.00
inventory 500g
10-20 days ฿123,000.00

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Fmoc chloride
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Fmoc chloride is widely used in peptide synthesis as a protecting group for amino acids. It reacts with the amino group to form an Fmoc-protected amino acid, which prevents unwanted side reactions during peptide chain assembly. This protection is crucial in solid-phase peptide synthesis (SPPS), where the Fmoc group can be easily removed under mild basic conditions, allowing for sequential addition of amino acids. Its stability and selective deprotection make it a preferred choice in the production of com

Fmoc chloride is widely used in peptide synthesis as a protecting group for amino acids. It reacts with the amino group to form an Fmoc-protected amino acid, which prevents unwanted side reactions during peptide chain assembly. This protection is crucial in solid-phase peptide synthesis (SPPS), where the Fmoc group can be easily removed under mild basic conditions, allowing for sequential addition of amino acids. Its stability and selective deprotection make it a preferred choice in the production of complex peptides and proteins for pharmaceutical and biochemical research. Additionally, Fmoc chloride is employed in the synthesis of other organic compounds where temporary protection of amine groups is required.

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