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 |
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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 |
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1.000 | 10-20 days | ฿330.00 |
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5.000 | 10-20 days | ฿880.00 |
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25.000 | 10-20 days | ฿4,350.00 |
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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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