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Diisopropyl ether is used as a specialized solvent to remove or extract polar organic compounds from aqueous solutions, e.g. phenols, ethanol, acetic acid. It has also been used as an antiknock agent. In the laboratory, diisopropyl ether is useful for recrystallizations because it has a wide liquid range. [4] [5] Diisopropyl ether is used for ...
As is typical of ethers, dipropyl ether may slowly form explosive organic peroxides over long periods in storage. [2] Antioxidants such as butylated hydroxytoluene are often added to ethers to prevent this process. [4] Due to the shock and light sensitive nature of organic peroxides, dipropyl ether should never be boiled or evaporated to dryness.
Diisopropyl ether-60 Dry ice: Chloroform-61 Liquid N 2: Chloroform-63 [2] Dry ice: Ethanol-72 Note: without the addition of ethylene glycol, temp is -78 °C. Dry ice: Trichloroethylene-73 Dry ice: Isopropyl alcohol-77 Liquid N 2: Butyl acetate-77 Dry ice: Acetone-78 Liquid N 2: Isoamyl acetate-79 Dry ice: Sulfur dioxide-82 Liquid N 2: Ethyl ...
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Fuel additives in the United States are regulated under section 211 of the Clean Air Act (as amended in January 1995). The Environmental Protection Agency (EPA) requires the registration of all fuel additives which are commercially distributed for use in highway motor vehicles in the United States, [8] and may require testing and ban harmful additives.
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All the common ethers, including diethyl ether, tetrahydrofuran (THF) and diisopropyl ether contain a CH group adjacent to the oxygen. The first two are primary ethers containing CH 2 groups adjacent to the oxygen, while diisopropyl ether is a secondary ether. THF and diethyl ether are very widely used as solvents, with precautions recommended ...