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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.

3. Compression stockings - Wikipedia

   en.wikipedia.org/wiki/Compression_stockings

   Compression stockings are constructed using elastic fibers or rubber. These fibers help compress the limb, aiding in circulation. Compression stockings are offered in different levels of compression. The unit of measure used to classify the pressure of the stockings is mmHg. They are often sold in a variety of pressure ranges. [citation needed]

4. 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

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. 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]