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  2. Polydimethylsiloxane - Wikipedia

    en.wikipedia.org/wiki/Polydimethylsiloxane

    The chemical formula of PDMS is CH 3 [Si(CH 3) 2 O] n Si(CH 3) 3, where n is the number of repeating monomer [Si(CH 3) 2 O] units. [4] Industrial synthesis can begin from dimethyldichlorosilane and water by the following net reaction:

  3. List of alkanols - Wikipedia

    en.wikipedia.org/wiki/List_of_alkanols

    Unsourced material may be challenged and removed ... 2,3-Dimethyl-1-butanol; 3,3-Dimethyl-1-butanol This page was last edited on 27 March 2024, at 19:55 ...

  4. Octanol - Wikipedia

    en.wikipedia.org/wiki/Octanol

    A simple and important member is 1-octanol, with an unbranched chain of carbons. Other commercially important octanols are 2-octanol and 2-ethylhexanol . Some octanols occur naturally in the form of esters in some essential oils.

  5. Dimethyl sulfoxide (data page) - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfoxide_(data_page)

    1 Material Safety Data Sheet. 2 Structure and properties. 3 Thermodynamic properties. ... for dimethyl sulfoxide/water [4] P = 550 mm Hg BP Temp. °C % by mole water ...

  6. Dimethyloctadecyl(3-trimethoxysilylpropyl)ammonium chloride

    en.wikipedia.org/wiki/Dimethyloctadecyl(3...

    This page was last edited on 12 December 2024, at 07:10 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  7. Tetrakis(dimethylamido)titanium - Wikipedia

    en.wikipedia.org/wiki/Tetrakis(dimethylamido...

    Tetrakis(dimethylamino)titanium (TDMAT), also known as Titanium(IV) dimethylamide, is a chemical compound.The compound is generally classified as a metalorganic species, meaning that its properties are strongly influenced by the organic ligands but the compound lacks metal-carbon bonds.

  8. Dimethoxymethane - Wikipedia

    en.wikipedia.org/wiki/Dimethoxymethane

    It can be manufactured by oxidation of methanol or by the reaction of formaldehyde with methanol. In aqueous acid, it is hydrolyzed back to formaldehyde and methanol.. Due to the anomeric effect, dimethoxymethane has a preference toward the gauche conformation with respect to each of the C–O bonds, instead of the anti conformation.

  9. Dimethylaminoethyl acrylate - Wikipedia

    en.wikipedia.org/wiki/Dimethylaminoethyl_acrylate

    The most significant use for DMAEA is the quaternization with alkylating agents (for example chloromethane, dimethyl sulfate or benzyl chloride) to the quaternary ammonium salt. [9] Quaternisierung von Dimethylaminoethylacrylat. The most important compound is the reaction product with methyl chloride, trimethylammonium ethyl acrylate chloride. [10]