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  2. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.

  3. Disodium hydrogen arsenate - Wikipedia

    en.wikipedia.org/wiki/Disodium_hydrogen_arsenate

    Disodium hydrogen arsenate is highly toxic. The salt is the conjugate base of arsenic acid. It is a white, water-soluble solid. [1] Being a diprotic acid, its acid-base properties is described by two equilibria: H 2 AsO − 4 + H 2 O ⇌ HAsO 2− 4 + H 3 O + (pK a2 = 6.94) HAsO 2− 4 + H 2 O ⇌ AsO 3− 4 + H 3 O + (pK a3 = 11.5)

  4. Selenous acid - Wikipedia

    en.wikipedia.org/wiki/Selenous_acid

    Selenous acid is analogous to sulfurous acid, but it is more readily isolated. Selenous acid is easily formed upon the addition of selenium dioxide to water. As a crystalline solid, the compound can be seen as pyramidal molecules that are interconnected with hydrogen bonds. In solution it is a diprotic acid: [3] H 2 SeO 3 ⇌ H + + HSeO − 3 ...

  5. Phosphorous acid - Wikipedia

    en.wikipedia.org/wiki/Phosphorous_acid

    Phosphorous acid (or phosphonic acid) is the compound described by the formula H 3 PO 3. This acid is diprotic (readily ionizes two protons), not triprotic as might be suggested by this formula. Phosphorous acid is an intermediate in the preparation of other phosphorus compounds.

  6. List of saturated fatty acids - Wikipedia

    en.wikipedia.org/wiki/List_of_saturated_fatty_acids

    Common Name Systematic Name Structural Formula Lipid Numbers Propionic acid: Propanoic acid CH 3 CH 2 COOH C3:0 Butyric acid: Butanoic acid CH 3 (CH 2) 2 COOH C4:0 Valeric acid: Pentanoic acid CH 3 (CH 2) 3 COOH C5:0 Caproic acid: Hexanoic acid CH 3 (CH 2) 4 COOH C6:0 Enanthic acid: Heptanoic acid CH 3 (CH 2) 5 COOH C7:0 Caprylic acid: Octanoic ...

  7. Tartaric acid - Wikipedia

    en.wikipedia.org/wiki/Tartaric_acid

    The acid itself is added to foods as an antioxidant E334 and to impart its distinctive sour taste. Naturally occurring tartaric acid is a useful raw material in organic synthesis. Tartaric acid, an alpha-hydroxy-carboxylic acid, is diprotic and aldaric in acid characteristics and is a dihydroxyl derivative of succinic acid.

  8. Squaric acid - Wikipedia

    en.wikipedia.org/wiki/Squaric_acid

    Squaric acid, also called quadratic acid because its four carbon atoms approximately form a square, is a diprotic organic acid with the chemical formula C 4 O 2 (OH) 2. [4]The conjugate base of squaric acid is the hydrogensquarate anion HC 4 O − 4; and the conjugate base of the hydrogensquarate anion is the divalent squarate anion C 4 O 2− 4.

  9. Dicarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Dicarboxylic_acid

    This acid is also produced when castor oil is oxidised. Suberic acid is used in the manufacture of alkyd resins and in the synthesis of polyamides (nylon variants). Azelaic acid's name stems from the action of nitric acid (azote, nitrogen, or azotic, nitric) oxidation of oleic acid or elaidic acid. It was detected among products of rancid fats.