Ethyl pyruvate

This study concluded three things: First, ethyl pyruvate prevents the severe acute pancreatitis-induced hepatic expression of tumor necrosis factor α (TNF-α) and interleukin-1β (IL-1β).

This experiment concluded that the pyruvate treatments proved beneficial neurologically post-cortical contusion injury (CCI).

Ethyl pyruvate is a good antioxidant due to its α-ketocarboxylate structure, which allows it to reduce hydrogen peroxide to water and scavenge the hydroxyl radical through decarboxylation.

[10] Overall, ethyl pyruvate has been found to be beneficial in wound healing, liver disease, pancreatitis, and spinal cord repair.

Relating to health, there are still many researchers using ethyl pyruvate in their projects pertaining to myocardial ischemia, reperfusion, and human gastric cancer.

There are many different reagents that can be used to push the reaction forward to yield in excess of 98%, such as using potassium permanganate and aluminum sulfate hydrate in dichloromethane solvent.

Enantioselective reactions are extremely important in chemistry, as the formation of optically pure products is especially useful in the food, pharmaceutical, and agrochemical industries.

NFPA 704 four-colored diamond Health 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroform Flammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuel Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen Special hazards (white): no code
"Mechanism of Ethyl Pyruvate formation"