Phospho(enol)pyruvic acid monopotassium salt , 97% , 4265-07-0
Synonym(s):
2-(Phosphonooxy)-2-propenoic acid monopotassium salt;mono-Potassium phosphoenolpyruvate;PEP monopotassium salt;PEP-K;Phospho(enol)pyruvate potassium salt
CAS NO.：4265-07-0
Empirical Formula: C3H4KO6P
Molecular Weight: 206.13
MDL number: MFCD00044476
EINECS: 224-247-0
| Pack Size | Price | Stock | Quantity |
| 250MG | RMB79.20 | In Stock |
|
| 1G | RMB158.40 | In Stock |
|
| 5G | RMB599.20 | In Stock |
|
| 25g | RMB2383.20 | In Stock |
|
| others | Enquire |
PRODUCT Properties
| Melting point: | 175 °C (dec.)(lit.) |
| storage temp. | 2-8°C |
| solubility | Methanol (Slightly), Water (Slightly) |
| form | solid |
| color | White to off-white |
| Water Solubility | Soluble in water. Slightly soluble in methanol. |
| Sensitive | Hygroscopic |
| BRN | 4603446 |
| CAS DataBase Reference | 4265-07-0(CAS DataBase Reference) |
| EPA Substance Registry System | 2-Propenoic acid, 2-(phosphonooxy)-, monopotassium salt (4265-07-0) |
Description and Uses
Phosphoenolpyruvic acid plays a role in both glycolysis and gluconeogenesis. During glycolysis, it is formed by the action of enolase on 2-phosphoglycerate and is metabolized to pyruvate by pyruvate kinase. One molecule of ATP is formed during its metabolism in this pathway. During gluconeogenesis, it is formed from phosphoenolpyruvate carboxykinase-catalyzed oxaloacetate decarboxylation and GTP hydrolysis. In plants, it is metabolized to form aromatic amino acids and also serves as a substrate for phosphoenolpyruvate carboxylase-catalyzed carbon fixation.
Substrate for many kinase reactions.
Safety
| Symbol(GHS) |  GHS07 |
| Signal word | Warning |
| Hazard statements | H315-H319-H335 |
| Precautionary statements | P261-P271-P280 |
| Safety Statements | 24/25 |
| WGK Germany | 3 |
| F | 3-10 |
| TSCA | Yes |
| HS Code | 29199000 |
