Fmoc chloride

98%

Reagent Code: #78365
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

Used primarily in peptide synthesis, it serves as a protecting group for amino acids. The compound reacts with the amino group, forming an Fmoc-protected amino acid, which is stable under various reaction conditions. This protection is crucial during the stepwise construction of peptides, allowing selective deprotection without affecting other functional groups. It is widely employed in solid-phase peptide synthesis, enabling the production of complex peptides and proteins. Additionally, it finds use in the synthesis of organic compounds where temporary amine protection is required. Its versatility and efficiency make it a valuable tool in both research and industrial applications.

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Test Parameter Specification
Melting point 61-65
Purity (HPLC) 98-100
Purity (Titration with AgNO3) 97.5-102.5
Appearance White to yellow powder or crystals

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500g
10-20 days ฿11,380.00
inventory 5g
10-20 days ฿320.00
inventory 25g
10-20 days ฿790.00
inventory 100g
10-20 days ฿2,380.00
inventory 2.5kg
10-20 days ฿52,660.00

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Fmoc chloride
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Used primarily in peptide synthesis, it serves as a protecting group for amino acids. The compound reacts with the amino group, forming an Fmoc-protected amino acid, which is stable under various reaction conditions. This protection is crucial during the stepwise construction of peptides, allowing selective deprotection without affecting other functional groups. It is widely employed in solid-phase peptide synthesis, enabling the production of complex peptides and proteins. Additionally, it finds use in the synthesis of organic compounds where temporary amine protection is required. Its versatility and efficiency make it a valuable tool in both research and industrial applications.
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