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(2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexanal

Base Information Edit
  • Chemical Name:(2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexanal
  • CAS No.:1990-29-0
  • Molecular Formula:C6H12 O6
  • Molecular Weight:180.158
  • Hs Code.:29400090
  • European Community (EC) Number:217-870-4
  • UNII:5PLN1O36FF
  • DSSTox Substance ID:DTXSID10894871
  • Nikkaji Number:J14.385E
  • Wikidata:Q423207
  • Metabolomics Workbench ID:51700
  • Mol file:1990-29-0.mol
(2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexanal

Synonyms:1990-29-0;(2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexanal;D(+)-Altrose;UNII-5PLN1O36FF;5PLN1O36FF;Altrose, D-;EINECS 217-870-4;NSC-2573;aldehydo-D-altrose;D-ALRTOSE;D-ALTROSE [MI];ALTROSE, (+)-;SCHEMBL15894565;DTXSID10894871;NSC 2573;AKOS027320138;HY-W145652;CS-0226081;Q423207;WURCS=2.0/1,1,0/[o1222h]/1/;41846-94-0;5987-68-8

Suppliers and Price of (2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexanal
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
  • D-Altrose
  • 10mg
  • $ 403.00
  • Usbiological
  • D-Altrose
  • 50mg
  • $ 340.00
  • Usbiological
  • D-Altrose
  • 250mg
  • $ 360.00
  • TRC
  • D-Altrose
  • 10mg
  • $ 110.00
  • Sigma-Aldrich
  • D-Altrose ≥97.0% (HPLC)
  • 50mg
  • $ 123.00
  • Medical Isotopes, Inc.
  • D-(+)-Altrose >97%
  • 10 mg
  • $ 580.00
  • Crysdot
  • (2S,3R,4R,5R)-2,3,4,5,6-Pentahydroxyhexanal 95+%
  • 1g
  • $ 342.00
  • Chemenu
  • D-ALTROSE 95%
  • 1g
  • $ 416.00
  • Biosynth Carbosynth
  • D-Altrose
  • 500 mg
  • $ 135.00
  • Biosynth Carbosynth
  • D-Altrose
  • 250 mg
  • $ 80.00
Total 31 raw suppliers
Chemical Property of (2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexanal Edit
Chemical Property:
  • Vapor Pressure:1.83E-08mmHg at 25°C 
  • Melting Point:106-108 °C  
  • Refractive Index:1.5860 (estimate) 
  • Boiling Point:527.1°Cat760mmHg 
  • PKA:12.45±0.20(Predicted) 
  • Flash Point:286.7°C 
  • PSA:118.22000 
  • Density:1.581g/cm3 
  • LogP:-3.37880 
  • Storage Temp.:2-8°C 
  • Solubility.:DMSO (Slightly), Methanol (Slightly, Heated), Water (Slightly) 
  • XLogP3:-2.9
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:5
  • Exact Mass:180.06338810
  • Heavy Atom Count:12
  • Complexity:138
Purity/Quality:

98%, *data from raw suppliers

D-Altrose *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 24/25-36-26 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C(C(C(C(C(C=O)O)O)O)O)O
  • Isomeric SMILES:C([C@H]([C@H]([C@H]([C@@H](C=O)O)O)O)O)O
  • Uses D-Altrose is the epimer of D-glucose at C3 and have recently been discovered to possess antioxidant properties by the suppression of reactive oxygen species production in mitochondria due to competiti on with D-glucose at the cellular level.
Technology Process of (2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexanal

There total 122 articles about (2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexanal 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:
D-psicose; With 2-aminopyridine; acetic acid; at 90 ℃; Sealed tube;
2-aminopyridine; With acetic acid; at 90 ℃; Sealed tube;
With trifluoroacetic acid; at 65 ℃; for 1h;
DOI:10.1016/j.carres.2011.09.021
Guidance literature:
D-Allose; With aluminum oxide; In pyridine; for 2h; Heating;
With sulfuric acid; In acetone; for 2h; Further stages.;
DOI:10.1016/j.carres.2007.05.033
Guidance literature:
With 4-methylmorpholine N-oxide; at 110 ℃; Product distribution;
DOI:10.1016/j.carres.2004.06.004
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