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CasNo: 131-48-6
MF: C11H19NO9
Appearance: Crystalline
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N-acetylneuraminic acid is an N-acyl derivative of neuraminic or acid amino sugar derivative, derived from N-acetylmannosamine and pyruvic acid. It is an important constituent of glycoproteins and glycolipids. N-acetylneuraminic acid occurs in many polysaccharides, glycoproteins, and glycolipids in animals and bacteria.
N-Acetylneuraminic acid is an integral part of sialic acids (SAs), important functional sugars that play an important role in maintaining and improving brain health, detoxification, antibacterial, and immune enhancement. n-Acetylneuraminic acid is biologically useful for neurotransmission, leukocyte extravasation, viral or bacterial infection, and carbohydrate-protein recognition. n- Acetylneuraminic acid is used to study its biochemistry, metabolism and absorption in vivo and in vitro.
The CAS number of N-Acetylneuraminic acid is 131-48-6.
More information of N-Acetylneuraminic acid 131-48-6 are:
CAS Number |
131-48-6 |
Density |
1.727 g/cm3 |
Melting Point |
184-186 °C |
Boiling Point |
395.6 °C at 760 mmHg |
Flash Point |
193 °C |
Vapor Pressure |
5.5E-30mmHg at 25°C |
Refractive Index |
-32 ° (C=1, H2O) |
HS CODE |
29329970 |
PSA |
176.78000 |
LogP |
-3.48090 |
Pka |
2.41±0.54(Predicted) |
The chemical formula of N-Acetylneuraminic acid is C11H19NO9 which containing 11 Carbon atoms,19 Hydrogen atoms,1 Nitrogen atoms and 9 Oxygen atoms,and the molecular weight, and the molecular weight of N-Acetylneuraminic acid is 309.273
N-acetylneuraminic acid is an N-acyl derivative of neuraminic or acid amino sugar derivative, derived from N-acetylmannosamine and pyruvic acid. It is an important constituent of glycoproteins and glycolipids. N-acetylneuraminic acid occurs in many polysaccharides, glycoproteins, and glycolipids in animals and bacteria.
InChI:InChI=1/C11H19NO9/c1-4(14)12-7-5(15)2-11(20,10(18)19)21-9(7)8(17)6(16)3-13/h5-9,13,15-17,20H,2-3H2,1H3,(H,12,14)(H,18,19)/t5-,6+,7+,8+,9+,11-/m0/s1
Relevant articles related to N-Acetylneuraminic acid:
Article |
Source |
Uncovering a novel molecular mechanism for scavenging sialic acids in bacteria |
Angulo, Jesus,Bell, Andrew,Juge, Nathalie,Latousakis, Dimitrios,Lee, Micah,Monaco, Serena,Naismith, James H.,Severi, Emmanuele,Thomas, Gavin H. , p. 13724 - 13736 (2020) |
Three-step synthesis of sialic acids and derivatives |
Hong, Zhangyong,Liu, Lei,Hsu, Che-Chang,Wong, Chi-Huey , p. 7417 - 7421 (2007/10/03) |
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