Glycidol is an organic compound with the formula HOCH 2 CHOCH 2. The molecule contains both epoxide and alcohol functional groups . Being simple to make and bifunctional, it has a variety of industrial uses.

2021年12月21日 · Glycidol is an epoxide alcohol that is a colorless, slightly viscous liquid at room temperature . It is miscible with water, alcohols, esters, ketones, ethers, and aromatics and almost insoluble in aliphatic hydrocarbons. Glycidol may decompose upon exposure to moisture .

Glycidol | C3H6O2 | CID 11164 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

Glycidol is an alkylating agent which reacts readily with glutathione. It causes a decrease in glutathione content in rat liver, probably reflecting its binding to glutathione. In rats, it is metabolized to oxidative and glutathione-derived products.

2019年9月16日 · Glycidol is an epoxide and an alcohol, and as such is a highly reactive compound. It is miscible with water but also reacts with it. It decomposes when distilled at atmospheric pressure. In 1909, chemist Nikolai Prilezhaev at the Warsaw University of Technology prepared glycidol by epoxidizing allyl alcohol with peroxybenzoic acid.

Glycidol is a small molecule possessing a chemically reactive epoxide group. Therefore, it acts as a direct alkylating agent. Nucleophilic bioactive compounds such as glutathione react readily with glycidol. Glycidol decreases glutathione content in rat liver by direct binding to the glutathione.

2021年1月28日 · ACGIH: Documentation of the Threshold Limit Values (TLVs) and Biological Exposure Indices (BEIs) - Glycidol. See annual publication for most recent information. No Author: Glycidol. Report on Carcinogens (latest edition); U.S. Department of Health and Human Services, Public Health Service, National Toxicology Program.