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Technology Process of Glucosylgalactosylhydroxylysine

Glucosylgalactosylhydroxylysine

Base Information
  • Chemical Name:Glucosylgalactosylhydroxylysine
  • CAS No.:32448-35-4
  • Molecular Formula:C18H34 N2 O13
  • Molecular Weight:486.47
  • Hs Code.:
  • Wikidata:Q27161771
  • Metabolomics Workbench ID:37322
  • Mol file:32448-35-4.mol
Glucosylgalactosylhydroxylysine

Synonyms:1,2 alpha-glucosylgalactosyl-O-hydroxylysine;glucosylgalactosylhydroxylysine;hydroxylysine-galactose-glucose;hydroxylysine-glucose-galactose

Suppliers and Price of Glucosylgalactosylhydroxylysine
Supply Marketing:
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
  • TRC
  • 5-[(2-O-A-D-Glucopyranosyl-b-D-galactopyranosyl)oxy]-L-lysine
  • 50mg
  • $ 17160.00
  • TRC
  • 5-[(2-O-A-D-Glucopyranosyl-b-D-galactopyranosyl)oxy]-L-lysine
  • 10mg
  • $ 4070.00
Total 27 raw suppliers
Chemical Property of Glucosylgalactosylhydroxylysine
Chemical Property:
  • Vapor Pressure:2.47E-29mmHg at 25°C 
  • Refractive Index:1.646 
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA：267.87000 
  • Density:g/cm3 
  • LogP:-4.45290 
  • XLogP3:-7.4
  • Hydrogen Bond Donor Count:10
  • Hydrogen Bond Acceptor Count:15
  • Rotatable Bond Count:11
  • Exact Mass:486.20608914
  • Heavy Atom Count:33
  • Complexity:616
Purity/Quality:

97% *data from raw suppliers

5-[(2-O-A-D-Glucopyranosyl-b-D-galactopyranosyl)oxy]-L-lysine *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C(CC(C(=O)O)N)C(CN)OC1C(C(C(C(O1)CO)O)O)OC2C(C(C(C(O2)CO)O)O)O
  • Isomeric SMILES:C(CC(CN)O[C@H]1[C@@H]([C@H]([C@H]([C@H](O1)CO)O)O)O[C@@H]2[C@@H](C([C@@H]([C@H](O2)CO)O)O)O)[C@@H](C(=O)O)N
  • Uses 5-[(2-O-A-D-Glucopyranosyl-b-D-galactopyranosyl)oxy]-L-lysine is a bone formation and bone resorption marker that is related to bone turnover processes during growth and development as well as metabolic bone diseases; it is also involved with reactions associated with the functional expression of human mannan-binding proteins (MBPs) in human cell lines transfected with MBP cDNA.
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