N-Hydroxysuccinimide (6066-82-6): A Key Reagent in Peptide Synthesis and Organic Chemistry
Unlock efficient peptide synthesis and complex organic transformations with our high-purity N-Hydroxysuccinimide.
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N-Hydroxysuccinimide
N-Hydroxysuccinimide (NHS), identified by CAS number 6066-82-6, is a critical organic reagent renowned for its efficacy in activating carboxylic acids for amide bond formation. This makes it indispensable in peptide synthesis and other bioconjugation strategies. Its specific chemical properties and reactivity are leveraged extensively in the development of new pharmaceuticals and research chemicals.
- As a leading N-Hydroxysuccinimide CAS 6066-82-6 supplier, we ensure consistent quality for your synthesis needs.
- Leveraging N-Hydroxysuccinimide for efficient peptide synthesis allows for the creation of complex peptide chains.
- Exploring the use of organic reagent 6066-82-6 in novel chemical transformations can lead to groundbreaking discoveries.
- The availability of N-Hydroxysuccinimide for sale supports ongoing research and development in the life sciences.
Advantages Provided by the Product
Enhanced Reactivity for Amide Bonds
Utilizing N-Hydroxysuccinimide CAS 6066-82-6 as a coupling agent significantly boosts the efficiency of amide bond formation in complex molecules.
Facilitates Peptide Synthesis
The role of peptide synthesis reagent N-Hydroxysuccinimide is crucial for constructing stable and functional peptide sequences required for various biological applications.
Versatility in Organic Transformations
As a versatile organic reagent 6066-82-6, it enables a wide array of chemical modifications and synthesis pathways.
Key Applications
Peptide Synthesis
Buy N-Hydroxysuccinimide online to facilitate the creation of therapeutic peptides and research biochemicals.
Organic Synthesis
The application of N-Hydroxysuccinimide manufacturer China products aids in synthesizing complex organic molecules with defined structures.
Bioconjugation
Researchers often seek N-Hydroxysuccinimide for sale to perform protein labeling and create antibody-drug conjugates.
Chemical Research
As a fundamental amino acid derivative, it's essential for academic and industrial chemical research laboratories.