CAS 100-71-0: 2-Ethylpyridine

2-Ethylpyridine

2-Ethylpyridine is used to study its effect on the proliferation and survival of human umbilical vein endothelial cells (HUVECs), HMVECs from lung, and NIH 3T3 cells. 2-Ethylpyridine linked with silica is a popular stationary phase for chiral and achiral separations in supercritical fluid chromatography. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications 2-Ethylpyridine can be used to prepare Dimethindene Maleate (D460460). It is also used to study its effect on the proliferation and survival of human umbilical vein endothelial cells (HUVECs), HMVECs from lung, and NIH 3T3 cells.2-Ethylpyridine linked with silica is a popular stationary phase for chiral and achiral separations in supercritical fluid chromatography. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Richard, Y., et al.: Toxicol. Sci., 93, 82 (2006); Speybrouck, D., et a.: Curr. Topics in Med. Chem., 12, 1250(2012)

2-Ethylpyridine is a chemical compound that can be derived from sodium succinate, 2-ethylpyridine, and trifluoroacetic acid. It has been shown to have biological properties such as the inhibition of mitochondrial membrane potential, which is the driving force for ATP synthesis in mitochondria. This drug also inhibits the production of hydrogen peroxide and nitric oxide by reacting with hydrochloric acid or nitrogen atoms. 2-Ethylpyridine can be used as a solid catalyst for reactions involving hydrogen bond formation or intermolecular hydrogen bond formation. 2-Ethylpyridine reacts with protocatechuic acid to form an intramolecular hydrogen bond and a group p2 type of reaction mechanism.