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Encyclopedia

Gentianose

Base Information Edit
  • Chemical Name:Gentianose
  • CAS No.:25954-44-3
  • Molecular Formula:C18H32 O16
  • Molecular Weight:504.442
  • Hs Code.:
  • European Community (EC) Number:247-364-9
  • UNII:I0ZQ61S45F
  • DSSTox Substance ID:DTXSID401318513
  • Nikkaji Number:J17.211A
  • Wikidata:Q3100866
  • Metabolomics Workbench ID:51848
  • Mol file:25954-44-3.mol
Gentianose

Synonyms:Gentianose;25954-44-3;UNII-I0ZQ61S45F;I0ZQ61S45F;EINECS 247-364-9;(2R,3R,4S,5S,6R)-2-[[(2R,3S,4S,5R,6R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol;beta-D-Glcp-(1->6)-alpha-D-Glcp-(1<->2)-beta-D-Fruf;alpha-D-Glucopyranoside, beta-D-fructofuranosyl O-beta-D-glucopyranosyl-(1-->6)-;beta-D-fructofuranosyl O-beta-D-glucopyranosyl-(1-6)-alpha-D-glucopyranoside;O-beta-D-Glucopyranosyl-(1.6)-beta-D-fructofuranosyl-alpha-D-glucopyranoside;starbld0009596;CHEBI:28782;DTXSID401318513;HY-N8305;MFCD00064907;AKOS040759333;AC-34467;MS-29363;CS-0142902;C08239;Q3100866;W-202098;b-D-Glucopyranosyl-(1->6)-a-D-glucopyranosyl-(1->2)-b-D-fructofuranoside;beta-D-fructofuranosyl beta-D-glucopyranosyl-(1->6)-alpha-D-glucopyranoside;O-beta-D-glucopyranosyl-(16)-beta-D-fructofuranosyl-alpha-D-glucopyranoside;b-D-Fructofuranosyl O-b-D-glucopyranosyl-(1->6)-a-D-glucopyranoside, 9CI, 8CI;(2R,3R,4S,5S,6R)-2-((2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)tetrahydrofuran-2-yloxy)-6-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)methyl)tetrahydro-2H-pyran-3,4,5-triol;.ALPHA.-D-GLUCOPYRANOSIDE, .BETA.-D-FRUCTOFURANOSYL O-.BETA.-D-GLUCOPYRANOSYL-(1->6)-;WURCS=2.0/3,3,2/[a2122h-1a_1-5][ha122h-2b_2-5][a2122h-1b_1-5]/1-2-3/a1-b2_a6-c1

Suppliers and Price of Gentianose
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
  • Usbiological
  • Gentianose
  • 5mg
  • $ 409.00
  • TRC
  • Gentianose
  • 5mg
  • $ 195.00
  • Medical Isotopes, Inc.
  • Gentianose
  • 5 mg
  • $ 360.00
  • Biosynth Carbosynth
  • Gentianose
  • 25 mg
  • $ 92.50
  • Biosynth Carbosynth
  • Gentianose
  • 10 mg
  • $ 55.00
  • Biosynth Carbosynth
  • Gentianose
  • 50 mg
  • $ 150.00
  • Biosynth Carbosynth
  • Gentianose
  • 100 mg
  • $ 250.00
  • Biosynth Carbosynth
  • Gentianose
  • 250 mg
  • $ 412.50
  • American Custom Chemicals Corporation
  • GENTIANOSE 95.00%
  • 5MG
  • $ 499.88
  • AK Scientific
  • Gentianose
  • 25mg
  • $ 174.00
Total 13 raw suppliers
Chemical Property of Gentianose Edit
Chemical Property:
  • Melting Point:208-210oC 
  • Boiling Point:884.8oC at 760 mmHg 
  • PKA:12.81±0.70(Predicted) 
  • Flash Point:488.9oC 
  • PSA:268.68000 
  • Density:1.81g/cm3 
  • LogP:-7.57140 
  • Storage Temp.:Hygroscopic, -20°C Freezer, Under inert atmosphere 
  • Solubility.:Water (Slightly, Heated) 
  • XLogP3:-5.8
  • Hydrogen Bond Donor Count:11
  • Hydrogen Bond Acceptor Count:16
  • Rotatable Bond Count:8
  • Exact Mass:504.16903493
  • Heavy Atom Count:34
  • Complexity:655
Purity/Quality:

99% *data from raw suppliers

Gentianose *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O
  • Isomeric SMILES:C([C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@H](O2)O[C@]3([C@H]([C@@H]([C@H](O3)CO)O)O)CO)O)O)O)O)O)O)O
  • Uses Gentianose is a trisaccharide and phytochemical found in bitter gentian teas with antimicrobial, anti-inflammatory and antioxidant properties.
Technology Process of Gentianose

There total 8 articles about Gentianose 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 acetate buffer; spinach α-glucosidase I; at 37 ℃; for 4h; pH=5.0; Enzymatic reaction;
DOI:10.1271/bbb.67.1160

Reference yield:

Guidance literature:
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