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  2. Ethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_sulfate

    Ethyl sulfate can be produced in a laboratory setting by reacting ethanol with sulfuric acid under a gentle boil, while keeping the reaction below 140 °C. The sulfuric acid must be added dropwise or the reaction must be actively cooled because the reaction itself is highly exothermic.

  3. Phosphatidylethanol - Wikipedia

    en.wikipedia.org/wiki/Phosphatidylethanol

    After cessation of alcohol intake, the half-life of PEth is between 4.5 and 10 days in the first week and between 5 and 12 days in the second week. [2] As a blood marker PEth is more sensitive than carbohydrate deficient transferrin (CDT), urinary ethyl glucuronide (EtG) and ethyl sulfate (EtS). [8]

  4. Diethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_sulfate

    Although the formula for diethyl sulfate is typically written (C 2 H 5) 2 SO 4, a more descriptive formula would be (C 2 H 5 O) 2 SO 2. It is a diester of sulfuric acid. Sulfur is tetrahedral. Diethyl sulfate hydrolyzes readily, forming ethanol and ethyl sulfate. Eventually sulfuric acid is formed with excess water.

  5. Organosulfate - Wikipedia

    en.wikipedia.org/wiki/Organosulfate

    The SO 4 core is a sulfate group and the R group is any organic residue. All organosulfates are formally esters derived from alcohols and sulfuric acid (H 2 SO 4) although many are not prepared in this way. Many sulfate esters are used in detergents, and some are useful reagents.

  6. Vinyl sulfone dyes - Wikipedia

    en.wikipedia.org/wiki/Vinyl_sulfone_dyes

    (2-[(4-Aminophenyl)sulfonyl]ethyl hydrogen sulfate) Possible variations result from further substituents on the aromatic ring - usually hydroxy, methyl or methoxy groups - or from the position of the amino relative to the vinyl sulfone group. In addition to the para-substituted compound, also meta- and orthosubstituted vinyl sulfone anilines ...

  7. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    The tables below provides information on the variation of solubility of different substances (mostly inorganic compounds) in water with temperature, at one atmosphere pressure.

  8. Diethyl sulfide - Wikipedia

    en.wikipedia.org/wiki/Diethyl_sulfide

    Diethyl sulfide (British English: diethyl sulphide) is an organosulfur compound with the chemical formula (CH 3 CH 2) 2 S. It is a colorless, malodorous liquid. Although a common thioether, it has few applications.

  9. Lime sulfur - Wikipedia

    en.wikipedia.org/wiki/Lime_sulfur

    In horticulture, lime sulfur (lime sulphur in British English, see American and British English spelling differences) is mainly a mixture of calcium polysulfides and thiosulfate [1] (plus other reaction by-products as sulfite and sulfate) formed by reacting calcium hydroxide with elemental sulfur, used in pest control.