Fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate

98%

Reagent Code: #56710
label
Alias Tetramethylfluorourea hexafluorophosphate; Tetramethylfluorourea hexafluorophosphate, TFFH
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CAS Number 164298-23-1

science Other reagents with same CAS 164298-23-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.12 g/mol
Formula C₅H₁₂F₇N₂P
badge Registry Numbers
MDL Number MFCD02684443
thermostat Physical Properties
Melting Point 104-109 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C, away from light, dry

description Product Description

This chemical is widely used as a coupling reagent in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It facilitates the formation of peptide bonds between amino acids, ensuring high efficiency and minimal racemization. Its stability and reactivity make it a preferred choice for synthesizing complex peptides and proteins in pharmaceutical research and biotechnology. Additionally, it is employed in organic synthesis for activating carboxylic acids, enabling the formation of esters, amides, and other derivatives. Its application extends to the production of bioactive compounds and materials with specific functional properties.

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Test Parameter Specification
Melting point 104-110
Purity 98-100%
Water (Karl Fischer) 0-0.3%
Appearance White to off-white powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿4,980.00
inventory 1g
10-20 days ฿330.00
inventory 5g
10-20 days ฿1,250.00
inventory 100g
10-20 days ฿19,260.00

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Fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate
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This chemical is widely used as a coupling reagent in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It facilitates the formation of peptide bonds between amino acids, ensuring high efficiency and minimal racemization. Its stability and reactivity make it a preferred choice for synthesizing complex peptides and proteins in pharmaceutical research and biotechnology. Additionally, it is employed in organic synthesis for activating carboxylic acids, enabling the formation of esters

This chemical is widely used as a coupling reagent in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It facilitates the formation of peptide bonds between amino acids, ensuring high efficiency and minimal racemization. Its stability and reactivity make it a preferred choice for synthesizing complex peptides and proteins in pharmaceutical research and biotechnology. Additionally, it is employed in organic synthesis for activating carboxylic acids, enabling the formation of esters, amides, and other derivatives. Its application extends to the production of bioactive compounds and materials with specific functional properties.

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