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  2. Dipipanone - Wikipedia

    en.wikipedia.org/wiki/Dipipanone

    Dipipanone, sold under the brand names of Pipadone and Diconal [3] is a strong opioid analgesic drug, used for acute pain by mouth for adults. It is often used in instances where morphine is indicated but cannot be used due to the patient being allergic to morphine. In analgesic potency 25 mg dipipanone is approximately equivalent to 10 mg ...

  3. 1,3-Propanediol - Wikipedia

    en.wikipedia.org/wiki/1,3-Propanediol

    1,3-Propanediol is the organic compound with the formula CH 2 (CH 2 OH) 2. This 3-carbon diol is a colorless viscous liquid that is miscible with water. Products

  4. Bioseparation of 1,3-propanediol - Wikipedia

    en.wikipedia.org/wiki/Bioseparation_of_1,3...

    The three main types of chemicals in the fluid at this stage of the separation are water, BioPDO, and impurities such as glycerol, sugars, and proteins. Of the three chemicals water has the lowest boiling point (see the water, 1,3-propanediol, and glycerol articles for boiling point information), so it is removed as distillate in the first column.

  5. Neopentyl glycol - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_glycol

    Neopentyl glycol (IUPAC name: 2,2-dimethylpropane-1,3-diol) is an organic chemical compound. It is used in the synthesis of polyesters , paints , lubricants , and plasticizers . When used in the manufacture of polyesters, it enhances the stability of the product towards heat, light, and water.

  6. Pentaerythritol - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol

    Pentaerythritol was first reported in 1891 by German chemist Bernhard Tollens and his student P. Wigand. [5] It may be prepared via a base-catalyzed multiple-addition reaction between acetaldehyde and 3 equivalents of formaldehyde to give pentaerythrose (CAS: 3818-32-4), followed by a Cannizzaro reaction with a fourth equivalent of formaldehyde to give the final product plus formate ion.

  7. Propane-1,3-dithiol - Wikipedia

    en.wikipedia.org/wiki/Propane-1,3-dithiol

    Structure of (C 3 H 6 S 2) 2, the oxidized "dimer" of 1,3-propanedithiol. [4] 1,3-Propanedithiol is used in the synthesis of tiapamil. 1,3-Propanedithiol reacts with metal ions to form dithiolates. Illustrative is the synthesis of the derivative diiron propanedithiolate hexacarbonyl upon reaction with triiron dodecacarbonyl: [5] Fe 3 (CO) 12 ...

  8. Is Compounded Semaglutide Effective for Weight Loss? - AOL

    www.aol.com/compounded-semaglutide-effective...

    Plus, there was a 20 percent reduction in cardiovascular events. Just to hammer it home: These trials are on branded semaglutide — there are no official compounded semaglutide results.

  9. 1,3-propanediol dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/1,3-propanediol_dehydrogenase

    In enzymology, a 1,3-propanediol dehydrogenase (EC 1.1.1.202) is an enzyme that catalyzes the chemical reaction. propane-1,3-diol + NAD + 3-hydroxypropanal + NADH + H +. Thus, the two substrates of this enzyme are propane-1,3-diol and NAD +, whereas its 3 products are 3-hydroxypropanal, NADH, and H +.

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