Bromo-tris-pyrrolidinophosphonium hexafluorophosphate

98%

Reagent Code: #56696
label
Alias Tripyrrolidinylphosphonium bromide hexafluorophosphate
fingerprint
CAS Number 132705-51-2

science Other reagents with same CAS 132705-51-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 466.18 g/mol
Formula C₁₂H₂₄N₃P₂BrF₆
badge Registry Numbers
MDL Number MFCD00077412
thermostat Physical Properties
Melting Point 100 °C
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This chemical is widely used in peptide synthesis as a coupling reagent. It facilitates the formation of peptide bonds between amino acids, making it essential in the production of peptides for pharmaceutical and biochemical research. Its effectiveness in activating carboxyl groups ensures high yields and minimal racemization, which is critical for maintaining the integrity of synthesized peptides. Additionally, it is employed in organic synthesis for the preparation of amides, esters, and other complex molecules, owing to its stability and efficiency in promoting reactions under mild conditions. Its application extends to solid-phase peptide synthesis, where it enhances the stepwise assembly of peptide chains on solid supports.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (HPLC) 98-100
31P, 19F, 1H NMR Spectrum CONSISTENT
Appearance Colorless or white powder or crystals
Elemental Analysis (C H N P F Br) CONSISTENT
ESI consistent

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿390.00
inventory 5g
10-20 days ฿860.00
inventory 25g
10-20 days ฿3,600.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Bromo-tris-pyrrolidinophosphonium hexafluorophosphate
No image available

This chemical is widely used in peptide synthesis as a coupling reagent. It facilitates the formation of peptide bonds between amino acids, making it essential in the production of peptides for pharmaceutical and biochemical research. Its effectiveness in activating carboxyl groups ensures high yields and minimal racemization, which is critical for maintaining the integrity of synthesized peptides. Additionally, it is employed in organic synthesis for the preparation of amides, esters, and other complex

This chemical is widely used in peptide synthesis as a coupling reagent. It facilitates the formation of peptide bonds between amino acids, making it essential in the production of peptides for pharmaceutical and biochemical research. Its effectiveness in activating carboxyl groups ensures high yields and minimal racemization, which is critical for maintaining the integrity of synthesized peptides. Additionally, it is employed in organic synthesis for the preparation of amides, esters, and other complex molecules, owing to its stability and efficiency in promoting reactions under mild conditions. Its application extends to solid-phase peptide synthesis, where it enhances the stepwise assembly of peptide chains on solid supports.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...