Fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate
98%
- Product Code: 56710
Alias:
Tetramethylfluorourea hexafluorophosphate; Tetramethylfluorourea hexafluorophosphate, TFFH
CAS:
164298-23-1
Molecular Weight: | 264.12 g./mol | Molecular Formula: | C₅H₁₂F₇N₂P |
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EC Number: | MDL Number: | MFCD02684443 | |
Melting Point: | 104-109 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | 2~8°C, away from light, dry |
Product Description:
This chemical is widely used as a coupling reagent in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It facilitates the formation of peptide bonds between amino acids, ensuring high efficiency and minimal racemization. Its stability and reactivity make it a preferred choice for synthesizing complex peptides and proteins in pharmaceutical research and biotechnology. Additionally, it is employed in organic synthesis for activating carboxylic acids, enabling the formation of esters, amides, and other derivatives. Its application extends to the production of bioactive compounds and materials with specific functional properties.
Product Specification:
Test | Specification |
---|---|
Melting point | 104 110? |
Purity | 98 100% |
WATER BY KARL FISCHER | 0 0.3% |
APPEARANCE | WHITE TO OFF-WHITE POWDER OR CRYSTALS |
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 | ฿1,250.00 |
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25.000 | 10-20 days | ฿4,980.00 |
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100.000 | 10-20 days | ฿19,260.00 |
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Fluoro-N,N,N',N'-tetramethylformamidinium hexafluorophosphate
This chemical is widely used as a coupling reagent in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It facilitates the formation of peptide bonds between amino acids, ensuring high efficiency and minimal racemization. Its stability and reactivity make it a preferred choice for synthesizing complex peptides and proteins in pharmaceutical research and biotechnology. Additionally, it is employed in organic synthesis for activating carboxylic acids, enabling the formation of esters, amides, and other derivatives. Its application extends to the production of bioactive compounds and materials with specific functional properties.
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