O-(Benzotriazol-1-yl)-N,N,N',N'-bis(tetramethylene)uronium hexafluorophosphate

98%

Reagent Code: #126600
label
Alias (Benzotriazol-1-yl)-N,N,N',N'-dipyrrolylurea hexafluorophosphate
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CAS Number 105379-24-6

science Other reagents with same CAS 105379-24-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 431.32 g/mol
Formula C₁₅H₂₀F₆N₅OP
badge Registry Numbers
MDL Number MFCD00191770
thermostat Physical Properties
Melting Point 176 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This chemical is widely used in peptide synthesis as a coupling reagent. It facilitates the formation of amide bonds between amino acids, making it essential in the production of peptides and proteins in laboratory settings. Its high efficiency and ability to minimize racemization make it a preferred choice in solid-phase peptide synthesis. Additionally, it is employed in organic synthesis for activating carboxylic acids, enabling the formation of esters, amides, and other derivatives. Its stability and reactivity under mild conditions contribute to its versatility in various chemical reactions.

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Test Parameter Specification
Purity (HPLC) 98-100
Infrared Spectrometry Conforms To Structure
Proton NMR Spectrum Conforms To Structure
Melting Point 176°C (dec.) (lit.)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿300.00
inventory 1g
10-20 days ฿460.00
inventory 5g
10-20 days ฿1,950.00
inventory 25g
10-20 days ฿8,660.00

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O-(Benzotriazol-1-yl)-N,N,N',N'-bis(tetramethylene)uronium hexafluorophosphate
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This chemical is widely used in peptide synthesis as a coupling reagent. It facilitates the formation of amide bonds between amino acids, making it essential in the production of peptides and proteins in laboratory settings. Its high efficiency and ability to minimize racemization make it a preferred choice in solid-phase peptide synthesis. Additionally, it is employed in organic synthesis for activating carboxylic acids, enabling the formation of esters, amides, and other derivatives. Its stability and reactivity under mild conditions contribute to its versatility in various chemical reactions.
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