N-Acetylneuraminic acid CAS 131-48-6
  • N-Acetylneuraminic acid CAS 131-48-6N-Acetylneuraminic acid CAS 131-48-6

N-Acetylneuraminic acid CAS 131-48-6

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Product Description

Believe Chemical is a leading China N-Acetylneuraminic acid CAS 131-48-6 manufacturer, supplier and exporter. Adhering to the pursuit of perfect quality of products, so that our N-Acetylneuraminic acid CAS 131-48-6 have been satisfied by many customers. Shandong Believe Chemical Pte. Ltd. is a high-tech enterprise integrating R &D and sales of chemical technology. 

We are good at the advantages of chemical products in the field. Our products are exported to Europe, the United States, Japan, South Korea, Southeast Asia and other countries and regions. With science and technology as the guide, honesty as the foundation, quality as the life, and relying on the enterprise concept of innovation and development, we sincerely hope to establish exchanges and extensive cooperation with domestic and foreign customers to create prosperity!

N-Acetylneuraminic acid CAS 131-48-6 Chemical Specification 

Product Name

 N-Acetylneuraminic acid



Molecular Weight 










 White powder



99% 99.15%


The result conform with standard

N-Acetylneuraminic acid CAS 131-48-6 Chemical Properties

Melting point 184-186 ℃
Specific speed -32 º (c=2, water)
Boiling point 449.56 ℃ (rough estimate)
Density 1.3580 (rough estimate)
Refractive index -32 ° (c=1, H2O
Storage conditions -20 ° C
Solubility 50g/l (20 ℃)
Acidity coefficient (PKA) 2.41 ± 0.54 (predicted value)
Morphology, crystallization
Color: white

N-Acetylneuraminic acid CAS 131-48-6 Application

N-acetylneuraminic acid sialic acid (N-acyl neuraminic acid) is the most widely distributed sugar in nature, which is mainly composed of glycoproteins, glycolipids or bacterial capsule substances in animal cell membranes or secretions. In glycoproteins or glycolipids, the ketone group at position 2 forms a glycosidic bond, which makes it located at the non reducing end of the sugar side chain. Its negative charge or unique chemical structure makes it have various physiological specificity. The enzyme that hydrolyzes and removes terminal n-acetylneuraminidase (neuraminidase) is widely distributed in nature, from viruses to animals. Through the physiological activity changes of this enzyme chemicalbook, the role of this terminal acidic sugar residue has been clarified. For example, this sugar residue constitutes the binding site of influenza virus on the erythrocyte membrane and plays a major role in the mutual recognition between plasma glycoproteins and hepatocytes or the recognition mechanism of lymphocytes on the circulation pathway. Although the biosynthetic pathway is somewhat different in animals and bacteria, it all passes through N-acetylmannosamine or its 6-phosphate, which is catalyzed by specific pyrophosphatase and reacts with CTP to produce CMP-N-acetylneuraminic acid, which is incorporated into the sugar chain by glycosyl transfer reaction.

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