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D-Xylulose 5-phosphate

Base Information Edit
  • Chemical Name:D-Xylulose 5-phosphate
  • CAS No.:4212-65-1
  • Molecular Formula:C5H11O8P
  • Molecular Weight:230.111
  • Hs Code.:
  • UNII:6MF87847MR
  • DSSTox Substance ID:DTXSID60863330
  • Nikkaji Number:J652.282C
  • Wikipedia:Xylulose_5-phosphate
  • Wikidata:Q27094888
  • Metabolomics Workbench ID:37475
  • Mol file:4212-65-1.mol
D-Xylulose 5-phosphate

Synonyms:D-xylulose-5-phosphate;xylulose-5-phosphate;xylulose-5-phosphate, (D)-isomer

Suppliers and Price of D-Xylulose 5-phosphate
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
  • AccelPharmtech
  • D-Xylulose-5-phosphate 88.00%
  • 1G
  • $ 770.00
Total 3 raw suppliers
Chemical Property of D-Xylulose 5-phosphate Edit
Chemical Property:
  • Vapor Pressure:5.5E-18mmHg at 25°C 
  • Boiling Point:620.3°C at 760 mmHg 
  • Flash Point:329°C 
  • Density:1.812g/cm3 
  • Storage Temp.:Hygroscopic, -20°C Freezer, Under inert atmosphere 
  • Solubility.:Methanol (Slightly), Water 
  • XLogP3:-3.7
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:6
  • Exact Mass:230.01915430
  • Heavy Atom Count:14
  • Complexity:234
Purity/Quality:

D-Xylulose-5-phosphate 88.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C(C(C(C(=O)CO)O)O)OP(=O)(O)O
  • Isomeric SMILES:C([C@H]([C@@H](C(=O)CO)O)O)OP(=O)(O)O
  • Uses D-Xylulose 5-Phosphate, is a metabolite present in the hexose monophosphate pathway that activates the protein phosphatase 2A.
Technology Process of D-Xylulose 5-phosphate

There total 7 articles about D-Xylulose 5-phosphate 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 palladium 10% on activated carbon; hydrogen; In ethanol; at 20 ℃; for 24h; under 1810.07 Torr;
DOI:10.1002/ejoc.201601639
Guidance literature:
With D-xylulose kinase; Escherichia coli D-xylose isomerase; ATP; sodium hydroxide; pH=7.5; Enzymatic reaction;
DOI:10.1021/acscatal.5b02234
Guidance literature:
With thiamine pyrophosphate; magnesium chloride; S.cerevisiae transketolase; 0.1 M glycylglycine buffer, pH=7.6;
DOI:10.1016/S0040-4039(00)96770-4
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