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  2. Diisopropyl ether - Wikipedia

    en.wikipedia.org/wiki/Diisopropyl_ether

    Whereas at 20 °C, diethyl ether will dissolve 1% by weight water, diisopropyl ether dissolves 0.88%. 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.

  3. Methoxyethane - Wikipedia

    en.wikipedia.org/wiki/Methoxyethane

    Methoxyethane, also known as ethyl methyl ether, is a colorless gaseous ether with the formula CH 3 OCH 2 CH 3. Unlike the related dimethyl ether and diethyl ether, which are widely used and studied, this mixed alkyl ether has no current applications. It is a structural isomer of isopropyl alcohol.

  4. Isopropyl ether - Wikipedia

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

    This page was last edited on 2 January 2006, at 21:41 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may ...

  5. IPE - Wikipedia

    en.wikipedia.org/wiki/IPE

    Isopropyl ether, a chemical solvent, usually in the form of DIPE (diisopropyl ether) International political economy, an academic discipline; Integrity Policy Enforcement, a Linux Security Module (LSM) that enables additional security features

  6. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  7. Poly(N-isopropylacrylamide) - Wikipedia

    en.wikipedia.org/wiki/Poly(N-isopropylacrylamide)

    The synthesis of poly(N-isopropylacrylamide) began with the synthesis of the acrylamide monomer by Sprecht in 1956. [13]In 1957, Shearer patented the first application for what would be later identified as PNIPA for the use as a rodent repellent. [14]

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