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  2. Ethanethiol - Wikipedia

    en.wikipedia.org/wiki/Ethanethiol

    Ethanethiol was originally reported by Zeise in 1834. [7] Zeise treated calcium ethyl sulfate with a suspension of barium sulfide saturated with hydrogen sulfide. He is credited with naming the C 2 H 5 S- group as mercaptum. Ethanethiol can also be prepared by a halide displacement reaction, where ethyl halide is treated with aqueous sodium ...

  3. Voltage-gated proton channel - Wikipedia

    en.wikipedia.org/wiki/Voltage-gated_proton_channel

    Voltage-gated proton channels are ion channels that have the unique property of opening with depolarization, but in a strongly pH-sensitive manner. [1] The result is that these channels open only when the electrochemical gradient is outward, such that their opening will only allow protons to leave cells .

  4. Thiol - Wikipedia

    en.wikipedia.org/wiki/Thiol

    Such reactions are conducted in the presence of acidic catalysts. The other principal route to thiols involves the addition of hydrogen sulfide to alkenes. Such reactions are usually conducted in the presence of an acid catalyst or UV light. Halide displacement, using the suitable organic halide and sodium hydrogen sulfide has also been used. [23]

  5. Gating (electrophysiology) - Wikipedia

    en.wikipedia.org/wiki/Gating_(electrophysiology)

    When ion channels are in a 'closed' (non-conducting) state, they are impermeable to ions and do not conduct electrical current. When ion channels are in their open state, they conduct electrical current by allowing specific types of ions to pass through them, and thus, across the plasma membrane of the cell. Gating is the process by which an ...

  6. Voltage-gated ion channel - Wikipedia

    en.wikipedia.org/wiki/Voltage-gated_ion_channel

    Voltage-gated ion-channels are usually ion-specific, and channels specific to sodium (Na +), potassium (K +), calcium (Ca 2+), and chloride (Cl −) ions have been identified. [1] The opening and closing of the channels are triggered by changing ion concentration, and hence charge gradient, between the sides of the cell membrane. [2]

  7. Ethane-1,2-dithiol - Wikipedia

    en.wikipedia.org/wiki/Ethane-1,2-dithiol

    1,2-Ethanedithiol has been used as a scavenger in peptide cleavage synthesis. [citation needed] Like 1,3-propanedithiol, 1,2-ethanedithiol readily forms metal thiolate complexes. Illustrative is the synthesis of the derivative diiron ethanedithiolate hexacarbonyl upon reaction with triiron dodecacarbonyl: [5]

  8. Acetyl group - Wikipedia

    en.wikipedia.org/wiki/Acetyl_group

    In organic chemistry, an acetyl group is a functional group denoted by the chemical formula −COCH 3 and the structure −C(=O)−CH 3. It is sometimes represented by the symbol Ac [5] [6] (not to be confused with the element actinium). In IUPAC nomenclature, an acetyl group is called an ethanoyl group.

  9. Hydrogen ion - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_ion

    By definition, an acid is an ion or molecule that can donate a proton, and when introduced to a solution it will react with water molecules (H 2 O) to form a hydronium ion (H 3 O +), a conjugate acid of water. [4] For simplistic reasoning, the hydrogen ion (H +) is often used to abbreviate the hydronium ion.