enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Ethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_sulfate

    CH 3 CH 2 OH + H 2 SO 4 → CH 3 CH 2 OSO 3 H + H 2 O. If the temperature exceeds 140 °C, the ethyl sulfate product tends to react with residual ethanol starting material, producing diethyl ether. If the temperature exceeds 170 °C in a considerable excess of sulfuric acid, the ethyl sulfate breaks down into ethylene and sulfuric acid. [12] [13]

  3. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75

  4. Color Developing Agent 3 - Wikipedia

    en.wikipedia.org/wiki/Color_Developing_Agent_3

    The third in the series of color developing agents used in developing color films, commonly known as CD-3, is chemically known as N-[2-[(4-Amino-3-methylphenyl)ethylamino]ethyl]methanesulfonamide Sesquisulfate Monohydrate. [1]

  5. Diethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_sulfate

    In preparing ethyl esters of fatty acids, both equivalents of the ethyl electrophile are transferred, unlike the usual alkylation of phenoxides: [1] 2 RCO 2 Na + (C 2 H 5 O) 2 SO 2 → 2 RCO 2 C 2 H 5 + Na 2 SO 4. Both dimethyl sulfate and diethyl sulfate react with inorganic nucleophiles as well. For example, potassium iodide gives ethyl iodide.

  6. Ethanethiol - Wikipedia

    en.wikipedia.org/wiki/Ethanethiol

    Ethanethiol, commonly known as ethyl mercaptan, is an organosulfur compound with the formula CH 3 CH 2 SH. [5] It is a colorless liquid with a distinct odor. Abbreviated EtSH, it consists of an ethyl group (Et), CH 3 CH 2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in place of oxygen. The odor of ...

  7. Triethyloxonium tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Triethyloxonium_tetrafluo...

    4 Et 2 O·BF 3 + 2 Et 2 O + 3 C 2 H 3 OCH 2 Cl → 3 [Et 3 O] + [BF 4] − + B(OCH(CH 2 Cl)CH 2 OEt) 3. where the Et stands for ethyl. The trimethyloxonium salt is available from dimethyl ether via an analogous route. [6] These salts do not have long shelf-lives at room temperature. They degrade by hydrolysis: [Et 3 O] + [BF 4] − + H 2 O → ...

  8. tert-Butylthiol - Wikipedia

    en.wikipedia.org/wiki/Tert-Butylthiol

    tert-Butylthiol is the main ingredient in many gas odorant blends. [citation needed] It is always utilized as a blend of other compounds, typically dimethyl sulfide, methyl ethyl sulfide, tetrahydrothiophene or other mercaptans such as isopropyl mercaptan, sec-butyl mercaptan and/or n-butyl mercaptan, due to its rather high melting point of −0.5 °C (31.1 °F).

  9. 4-Ethylphenyl sulfate - Wikipedia

    en.wikipedia.org/wiki/4-Ethylphenyl_sulfate

    4-Ethylphenyl sulfate (4EPS) is a metabolite produced by gut bacteria, which can be toxic when present in large amounts. Elevated levels of this metabolite have been associated with some medical conditions including chronic kidney disease and autism .