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N-ACETYL-D-MANNOSAMINE

Base Information Edit
  • Chemical Name:N-ACETYL-D-MANNOSAMINE
  • CAS No.:4773-29-9
  • Molecular Formula:C8H15NO6
  • Molecular Weight:221.21
  • Hs Code.:
  • Mol file:4773-29-9.mol
N-ACETYL-D-MANNOSAMINE

Synonyms:Mannose,2-acetamido-2-deoxy- (6CI,8CI);N-Acetyl mannosamine;Acetyl-D-Mannosamine, N-;

Suppliers and Price of N-ACETYL-D-MANNOSAMINE
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • N-ACETYL-D-MANNOSAMINE 95.00%
  • 10G
  • $ 1963.50
  • American Custom Chemicals Corporation
  • N-ACETYL-D-MANNOSAMINE 95.00%
  • 1G
  • $ 693.00
Total 18 raw suppliers
Chemical Property of N-ACETYL-D-MANNOSAMINE Edit
Chemical Property:
  • Boiling Point:636.4 °C at 760 mmHg 
  • PKA:13.04±0.20(Predicted) 
  • Flash Point:338.7 °C 
  • PSA:127.09000 
  • Density:1.423 g/cm3  
  • LogP:-2.84410 
  • Storage Temp.:−20°C 
Purity/Quality:

98%, *data from raw suppliers

N-ACETYL-D-MANNOSAMINE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of N-ACETYL-D-MANNOSAMINE

There total 9 articles about N-ACETYL-D-MANNOSAMINE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With UDP-glucose 4-epimerase; N-acetylhexosamine 1-kinase; UDP-glucose-galactose 1-phosphate uridylyl transferase; ATP; magnesium chloride; at 30 ℃; for 120h; pH=6.5; aq. buffer; Enzymatic reaction;
DOI:10.1016/j.carres.2011.08.032
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