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  2. Diisopropyl ether - Wikipedia

    en.wikipedia.org/wiki/Diisopropyl_ether

    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 ...

  3. Isopropyl ether - Wikipedia

    en.wikipedia.org/?title=Isopropyl_ether&redirect=no

    Download as PDF; Printable version; In other projects Appearance. move to sidebar hide. From Wikipedia, the free encyclopedia. Redirect page. Redirect to: Diisopropyl ...

  4. Category:Symmetrical ethers - Wikipedia

    en.wikipedia.org/wiki/Category:Symmetrical_ethers

    Download QR code; Print/export Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... Diisopropyl ether; Dimethyl ether; Diphenyl ether;

  5. Di-n-propyl ether - Wikipedia

    en.wikipedia.org/wiki/Di-n-propyl_ether

    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.

  6. Di-tert-butyl ether - Wikipedia

    en.wikipedia.org/wiki/Di-tert-butyl_ether

    Download as PDF; Printable version; ... Di-tert-butyl ether is a tertiary ether, ... Diisopropyl ether; References

  7. Isopropyl chloride - Wikipedia

    en.wikipedia.org/wiki/Isopropyl_chloride

    Isopropyl chloride is an organic compound with the chemical formula (CH 3) 2 CHCl. It is a colourless to slightly yellow, volatile, flammable liquid with a sweet, ether-like (almost like petroleum) odour.

  8. N,N-Diisopropylethylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-Diisopropylethylamine

    DIPEA is a sterically hindered organic base that is commonly employed as a proton scavenger. Thus, like 2,2,6,6-tetramethylpiperidine and triethylamine, DIPEA is a good base but a poor nucleophile, DIPEA has low solubility in water, which makes it very easily recovered in commercial processes, a combination of properties that makes it a useful organic reagent.

  9. LFER solvent coefficients (data page) - Wikipedia

    en.wikipedia.org/wiki/LFER_solvent_coefficients...

    Coefficients for partition between water and solvents wet/dry solvent c e s a b v source w 1-butanol: 0.376 0.434 -0.718 -0.097 -2.350 2.682 [1]w