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  2. Fluoroantimonic acid - Wikipedia

    en.wikipedia.org/wiki/Fluoroantimonic_acid

    Fluoroantimonic acid is a mixture of hydrogen fluoride and antimony penta­fluoride, containing various cations and anions (the simplest being H 2 F + and Sb F − 6).This mixture is a superacid that, in terms of corrosiveness, is trillions of times stronger than pure sulfuric acid when measured by its Hammett acidity function.

  3. 3-Methylsalicylic acid - Wikipedia

    en.wikipedia.org/wiki/3-Methylsalicylic_acid

    3-Methylsalicylic acid is an organic compound with the formula CH 3 C 6 H 3 (CO 2 H)(OH). It is a white solid that is soluble in basic water and in polar organic solvents. At neutral pH, the acid exists as 3-methylsalicylate Its functional groups include a carboxylic acid and a phenol group.

  4. Sebacic acid - Wikipedia

    en.wikipedia.org/wiki/Sebacic_acid

    Sebacic acid is a naturally occurring dicarboxylic acid with the chemical formula HO 2 C(CH 2) 8 CO 2 H.It is a white flake or powdered solid. Sebaceus is Latin for tallow candle, sebum is Latin for tallow, and refers to its use in the manufacture of candles.

  5. Phthalic acid - Wikipedia

    en.wikipedia.org/wiki/Phthalic_acid

    In organic chemistry, phthalic acid is an aromatic dicarboxylic acid, with formula C 6 H 4 (CO 2 H) 2 and structure HO(O)C−C 6 H 4 −C(O)OH.Although phthalic acid is of modest commercial importance, the closely related derivative phthalic anhydride is a commodity chemical produced on a large scale. [4]

  6. Aleuritic acid - Wikipedia

    en.wikipedia.org/wiki/Aleuritic_acid

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  7. Malolactic fermentation - Wikipedia

    en.wikipedia.org/wiki/Malolactic_fermentation

    A winemaker running a paper chromatography test to determine whether a wine has completed malolactic fermentation. Malolactic conversion (also known as malolactic fermentation or MLF) is a process in winemaking in which tart-tasting malic acid, naturally present in grape must, is converted to softer-tasting lactic acid.

  8. Dodecanedioic acid - Wikipedia

    en.wikipedia.org/wiki/Dodecanedioic_acid

    DDDA has traditionally been produced from butadiene using a multi-step chemical process. [1] Butadiene is first converted to cyclododecatriene through cyclotrimerization. [2] The triene is then hydrogenated to cyclododecane. Autoxidation by air in the presence of boric acid gives a mixture of cyclodecanol and the cyclododecanone.

  9. Levulinic acid - Wikipedia

    en.wikipedia.org/wiki/Levulinic_acid

    The largest application of levulinic acid is its use in the production of aminolevulinic acid, a biodegradable herbicide used in South Asia. Another key application is the use of levulinic acid in cosmetics. Ethyl levulinate, a primary derivative of levulinic acid, is extensively used in fragrances and perfumes.