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  2. Citric acid - Wikipedia

    en.wikipedia.org/wiki/Citric_acid

    Citric acid sold in a dry powdered form is commonly sold in markets and groceries as "sour salt", due to its physical resemblance to table salt. It has use in culinary applications, as an alternative to vinegar or lemon juice, where a pure acid is needed. Citric acid can be used in food coloring to balance the pH level of a normally basic dye.

  3. Buffer solution - Wikipedia

    en.wikipedia.org/wiki/Buffer_solution

    In the case of citric acid, the overlap is extensive and solutions of citric acid are buffered over the whole range of pH 2.5 to 7.5. Calculation of the pH with a polyprotic acid requires a speciation calculation to be performed. In the case of citric acid, this entails the solution of the two equations of mass balance:

  4. Ion speciation - Wikipedia

    en.wikipedia.org/wiki/Ion_speciation

    Outside the transition range the concentration of acid or conjugate base is less than 10 % and the colour of the major species dominates. Species concentrations calculated with the program HySS for a 10 mM solution of citric acid. pK a1 = 3.13, pK a2 = 4.76, pK a3 = 6.40. A weak acid may be defined as an acid with pK a greater than

  5. Everything You Need to Know About Using Citric Acid for Skin

    www.aol.com/lifestyle/everything-know-using...

    A powerhouse ingredient for smoother skin. For premium support please call: 800-290-4726 more ways to reach us

  6. Amphibolic - Wikipedia

    en.wikipedia.org/wiki/Amphibolic

    The citric acid cycle (Krebs cycle) is a good example of an amphibolic pathway because it functions in both the degradative (carbohydrate, protein, and fatty acid) and biosynthetic processes. [2] The citric acid cycle occurs on the cytosol of bacteria and within the mitochondria of eukaryotic cells.

  7. Tricarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Tricarboxylic_acid

    A tricarboxylic acid is an organic carboxylic acid whose chemical structure contains three carboxyl functional groups (−COOH). The best-known example of a tricarboxylic acid is citric acid . Uses

  8. Acid strength - Wikipedia

    en.wikipedia.org/wiki/Acid_strength

    The strength of a weak organic acid may depend on substituent effects. The strength of an inorganic acid is dependent on the oxidation state for the atom to which the proton may be attached. Acid strength is solvent-dependent. For example, hydrogen chloride is a strong acid in aqueous solution, but is a weak acid when dissolved in glacial ...

  9. Anaplerotic reactions - Wikipedia

    en.wikipedia.org/wiki/Anaplerotic_reactions

    Malate, in the mitochondrial matrix, can be used to make pyruvate (catalyzed by malic enzyme) or oxaloacetic acid, both of which can enter the citric acid cycle. Glutamine can also be used to produce oxaloacetate during anaplerotic reactions in various cell types through "glutaminolysis," which is also seen in many c-Myc transformed cells. [3]