O-(2-Oxo-1(2H)pyridyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate

98%

  • Product Code: 56702
  Alias:    O-(1,2-dihydro-2-oxo-pyridyl)-1,1,3,3-tetramethylurea tetrafluoroborate
  CAS:    125700-71-2
Molecular Weight: 297.06 g./mol Molecular Formula: C₁₀H₁₆BF₄N₃O₂
EC Number: MDL Number: MFCD00075475
Melting Point: 140 °C (dec.)(lit.) Boiling Point:
Density: Storage Condition: 2~8°C, dry
Product Description: This chemical is widely used as a coupling reagent in peptide synthesis. It facilitates the formation of amide bonds between amino acids, making it essential in the production of peptides and proteins in both research and industrial settings. Its high reactivity and efficiency make it a preferred choice for solid-phase peptide synthesis, where it ensures minimal racemization and high yields. Additionally, it is employed in organic synthesis for the preparation of complex molecules, particularly in pharmaceutical development, where precise and efficient bond formation is critical. Its stability and compatibility with various solvents further enhance its utility in diverse chemical processes.
Product Specification:
Test Specification
Melting point 135 140?
PURITYHPLC 98 100%
APPEARANCE White crystalline powder
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days £7.46
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5.000 10-20 days £19.90
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25.000 10-20 days £98.38
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O-(2-Oxo-1(2H)pyridyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate
This chemical is widely used as a coupling reagent in peptide synthesis. It facilitates the formation of amide bonds between amino acids, making it essential in the production of peptides and proteins in both research and industrial settings. Its high reactivity and efficiency make it a preferred choice for solid-phase peptide synthesis, where it ensures minimal racemization and high yields. Additionally, it is employed in organic synthesis for the preparation of complex molecules, particularly in pharmaceutical development, where precise and efficient bond formation is critical. Its stability and compatibility with various solvents further enhance its utility in diverse chemical processes.
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