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Glyceric acid 1,3-biphosphate

Base Information Edit
  • Chemical Name:Glyceric acid 1,3-biphosphate
  • CAS No.:1981-49-3
  • Molecular Formula:C3H8O10P2
  • Molecular Weight:266.038
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50941636
  • Wikipedia:1,3-Bisphosphoglyceric_acid
  • Wikidata:Q1020557
  • Metabolomics Workbench ID:126754
  • ChEMBL ID:CHEMBL2074701
  • Mol file:1981-49-3.mol
Glyceric acid 1,3-biphosphate

Synonyms:1,3-biphosphoglycerate;1,3-biphosphoglyceric acid;1,3-bisphosphoglycerate;1,3-diphosphoglycerate;3-phosphoglyceroyl phosphate;glycerate 1,3-biphosphate

Suppliers and Price of Glyceric acid 1,3-biphosphate
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
Total 45 raw suppliers
Chemical Property of Glyceric acid 1,3-biphosphate Edit
Chemical Property:
  • Vapor Pressure:5.32E-19mmHg at 25°C 
  • Boiling Point:638.7°Cat760mmHg 
  • PKA:1.36±0.10(Predicted) 
  • Flash Point:340°C 
  • PSA:190.44000 
  • Density:2.143g/cm3 
  • LogP:-1.90750 
  • XLogP3:-3.9
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:10
  • Rotatable Bond Count:6
  • Exact Mass:265.95927044
  • Heavy Atom Count:15
  • Complexity:311
Purity/Quality:

98%,99%, *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C(C(C(=O)OP(=O)(O)O)O)OP(=O)(O)O
  • Uses Phosphono 2-hydroxy-3- phosphonooxypropanoate is a biological metabolite of glucose and can be involved in oncogenesis.
Technology Process of Glyceric acid 1,3-biphosphate

There total 22 articles about Glyceric acid 1,3-biphosphate 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 human phosphoglycerate kinase; magnesium chloride; diothiothreitol; In various solvent(s); at 25 ℃; pH=7.5; Enzyme kinetics;
DOI:10.1016/j.bcp.2004.06.012
Guidance literature:
With dipotassium hydrogenphosphate; NAD; glyceraldehyde-3-phosphate dehydrogenase; In various solvent(s); at 25 ℃; for 0.2h; pH=7.5;
DOI:10.1016/j.bcp.2004.06.012
Guidance literature:
With aldehyde dehydrogenase from Bacillus stearothermophilus; C22H28N7O16P3(4-); In aq. buffer; at 30 ℃; pH=8; Reagent/catalyst; Catalytic behavior; Enzymatic reaction;
DOI:10.1002/anie.202017027
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