Phosphoenolpyruvic acid cyclohexylammonium salt

Basic information

  • Product Name:Phosphoenolpyruvic acid cyclohexylammonium salt
  • CasNo.:10526-80-4
  • MF:C6H13N.C3H5O6P
  • MW:

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:
  • Packing:powder
  • Throughput:
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Product Details

CasNo: 10526-80-4

MF: C6H13N.C3H5O6P

Appearance: powder

Delivery Time: 15 days

Packing: 25kg/drum

Purity: 99%

  • Basic Information
    • English Name: Phosphoenolpyruvic acid cyclohexylammonium salt
    • CAS No.: 10526-80-4
    • Molecular Formula: C3​H4​O6​P⋅C6​H14​N
    • Molecular Weight: 267.22
  • Physicochemical Properties
    • Appearance: White to off - white powder.
    • Solubility: Easily soluble in water, with a solubility of 100mg/ml in water.
    • Melting Point: 148 - 150℃ (decomposition).
    • Stability: Sensitive to heat, should be stored at - 20℃ in a cool and dry place, protected from light.
  • Technical Indicators
    • Purity: Usually ≥97% (enzymatic method), and there are also products with a purity of 98%.
  • Uses
    • Biochemical Research: Phosphoenolpyruvic acid (PEP) is an important biochemical molecule in biological cells, containing a high - energy phosphate bond (-61.9 kJ/mol), and is involved in the processes of glycolysis and gluconeogenesis. In glycolysis, PEP is formed from 2 - phosphoglycerate by the action of enolase, and then converted into pyruvate by the catalysis of pyruvate kinase, while generating 1 molecule of ATP through substrate - level phosphorylation. In gluconeogenesis, PEP is formed from the decarboxylation of oxaloacetate and the hydrolysis of 1 molecule of GTP, and this reaction is catalyzed by phosphoenolpyruvate carboxykinase, which is the rate - limiting step in gluconeogenesis.
    • Plant Physiological Research: In plants, PEP can be used to synthesize chorismate through the shikimate pathway, and then be metabolized into aromatic amino acids (phenylalanine, tryptophan, and tyrosine) and other aromatic compounds. In addition, in C4 plants, PEP is an important substrate for carbon fixation. Under the catalysis of phosphoenolpyruvate carboxylase, PEP reacts with CO₂ to form oxaloacetate.