2-Chloro-1,3-dimethylimidazolidinium hexafluorophosphate

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Reagent Code: #56673
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CAS Number 101385-69-7

science Other reagents with same CAS 101385-69-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.56 g/mol
Formula C₅H₁₀ClF₆N₂P
badge Registry Numbers
MDL Number MFCD00191914
thermostat Physical Properties
Melting Point 231-233 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This chemical is primarily used as a coupling reagent in peptide synthesis. It facilitates the formation of peptide bonds between amino acids, making it valuable in the production of peptides for pharmaceutical and biochemical research. Its effectiveness in activating carboxyl groups ensures high yields and minimal side reactions, which is crucial for synthesizing complex peptides. Additionally, it is employed in organic synthesis for constructing amide bonds in various chemical reactions. Its stability and efficiency make it a preferred choice in laboratories focusing on peptide and organic chemistry.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 233-237
Purity (HPLC) 98-100
Purity (Titration with AgNO3) 97.5-102.5
Appearance White to light yellow powder
Infrared Spectrum Conforms to Structure
Solubility Clear, colorless (100 mg/mL (10%), CH3CN)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿2,230.00
inventory 1g
10-20 days ฿350.00
inventory 5g
10-20 days ฿860.00
inventory 100g
10-20 days ฿8,630.00

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2-Chloro-1,3-dimethylimidazolidinium hexafluorophosphate
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This chemical is primarily used as a coupling reagent in peptide synthesis. It facilitates the formation of peptide bonds between amino acids, making it valuable in the production of peptides for pharmaceutical and biochemical research. Its effectiveness in activating carboxyl groups ensures high yields and minimal side reactions, which is crucial for synthesizing complex peptides. Additionally, it is employed in organic synthesis for constructing amide bonds in various chemical reactions. Its stability

This chemical is primarily used as a coupling reagent in peptide synthesis. It facilitates the formation of peptide bonds between amino acids, making it valuable in the production of peptides for pharmaceutical and biochemical research. Its effectiveness in activating carboxyl groups ensures high yields and minimal side reactions, which is crucial for synthesizing complex peptides. Additionally, it is employed in organic synthesis for constructing amide bonds in various chemical reactions. Its stability and efficiency make it a preferred choice in laboratories focusing on peptide and organic chemistry.

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