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N,N,N,N-Tetramethyl-O-(N-succinimidyl)uronium hexafluorophosphate

CAS 265651-18-1

Molecular structure of N,N,N,N-Tetramethyl-O-(N-succinimidyl)uronium hexafluorophosphate

CAS · 265651-18-1

01

Product Overview

N,N,N,N-Tetramethyl-O-(N-succinimidyl)uronium hexafluorophosphate is a high-purity biochemical-reagents supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.

02

Product Specifications

Appearance: White to off-white crystal powder
Purity (HPLC): 99% min
Loss on drying: 0.5% max
03

Applications

This compound is primarily used as a peptide coupling reagent in solid-phase and solution-phase peptide synthesis. It promotes the formation of amide bonds between protected amino acids and peptides with high efficiency, enabling the construction of dipeptides, tripeptides, and longer peptide chains. It is also applied in medicinal chemistry and drug discovery for the synthesis of small molecules, amide-based drug candidates, and peptide derivatives. Additionally, it finds use in organic synthesis for forming amide and ester bonds in various functionalized molecules, including enzyme inhibitors, conjugates, and bioconjugation applications. Its efficiency in coupling reactions and minimal by-product formation make it suitable for both laboratory-scale synthesis and industrial peptide manufacturing.

04

Benefits

The benefits of N,N,N,N-Tetramethyl-O-(N-succinimidyl)uronium hexafluorophosphate include its high coupling efficiency, low racemization, and versatility. Its active uronium moiety ensures rapid activation of carboxylic acids and smooth amide bond formation with amines. The hexafluorophosphate counterion stabilizes the reagent and improves solubility in organic solvents, enhancing reaction reproducibility. Its use reduces side reactions and minimizes racemization of chiral centers, which is critical for producing biologically active peptides and chiral molecules. Furthermore, it is compatible with a wide range of protecting groups and reaction conditions, offering flexibility in complex synthesis protocols. The reagent's efficiency also reduces the quantity of reagents needed, improving cost-effectiveness and environmental sustainability.

05

Conclusion

In summary, N,N,N,N-Tetramethyl-O-(N-succinimidyl)uronium hexafluorophosphate is a highly effective coupling reagent widely used in peptide synthesis, medicinal chemistry, and organic synthesis. Its ability to promote rapid amide bond formation with minimal racemization, along with solubility and stability advantages, makes it indispensable for the synthesis of peptides, bioactive molecules, and complex amide-containing compounds. With its efficiency, versatility, and reliability, it supports high-quality and reproducible outcomes in both research and industrial applications.

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