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P0564 Sigma-Aldrich

Phospho(enol)pyruvic acid monosodium salt hydrate

≥97% (enzymatic)

Synonym: 2-(Phosphonooxy)-2-propenoic acid monosodium, Monosodium phosphoenolpyruvate, mono-Sodium phosphoenolpyruvate hydrate

  • CAS Number 53823-68-0 (anhydrous)

  • Empirical Formula (Hill Notation) C3H4NaO6P · xH2O

  • Molecular Weight 190.02 (anhydrous basis)

  •  Beilstein/REAXYS Number 4771585

  •  EC Number 258-810-7

  •  MDL number MFCD00150738

  •  PubChem Substance ID 57654496

  •  NACRES NA.22

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Properties

Related Categories Building Blocks, Chemical Synthesis, Organic Building Blocks, Organic Phosphates/Phosphites, Phosphorus Compounds More...
Quality Level   200
assay   ≥97% (enzymatic)
storage temp.   −20°C
SMILES string   O.[Na+].OC(=O)C(=C)OP(O)([O-])=O
InChI   1S/C3H5O6P.Na.H2O/c1-2(3(4)5)9-10(6,7)8;;/h1H2,(H,4,5)(H2,6,7,8);;1H2/q;+1;/p-1
InChI key   YEQQMAFLJISSCR-UHFFFAOYSA-M

Description

Packaging

1 g in poly bottle

100, 250 mg in poly bottle

Biochem/physiol Actions

Phospho(enol)pyruvic acid (PEP) is involved in glycolysis and gluconeogenesis. In glycolysis, PEP is metabolized by pyruvate kinase to yield pyruvate. In plants, PEP is involved in the formation of aromatic amino acids as well as in the carbon fixation pathway.

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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Certificate of Origin (COO)

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Protocols & Articles

Articles

Glycolysis via the Embden-Meyerhof-Parnas glycolytic pathway

Glycolysis is the almost universal pathway that converts glucose into pyruvate along with the formation of nicotinamide adenine dinucleotide (NADH) and adenosine triphosphate (ATP). It primarily occu...
Keywords: Aerobic, Aldol reaction, Anaerobic, Dehydration reaction, Fermentation, Glycolysis, Isomerizations, Metabolism, Metabolites, Metabolomics, Oxidations, Phosphorylations, Photosynthesis

Peer-Reviewed Papers
15

References

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