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  2. Phosphoric acids and phosphates - Wikipedia

    en.wikipedia.org/wiki/Phosphoric_acids_and...

    Since the ends are condensed, its formula has one less H 2 O (water) than tripolyphosphoric acid. The general formula of a phosphoric acid is H n−2x+2 P n O 3n−x+1, where n is the number of phosphorus atoms and x is the number of fundamental cycles in the molecule's structure; that is, the minimum number of bonds that would have to be ...

  3. Phosphoric acid - Wikipedia

    en.wikipedia.org/wiki/Phosphoric_acid

    Phosphoric acid (orthophosphoric acid, monophosphoric acid or phosphoric(V) acid) is a colorless, odorless phosphorus-containing solid, and inorganic compound with the chemical formula H 3 P O 4. It is commonly encountered as an 85% aqueous solution , which is a colourless, odourless, and non- volatile syrupy liquid.

  4. Triethyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Triethyl_phosphate

    Triethyl phosphate is an organic chemical compound with the formula (C 2 H 5) 3 PO 4 or OP(OEt) 3.It is a colorless liquid. It is the triester of ethanol and phosphoric acid and can be called "phosphoric acid, triethyl ester".

  5. Phosphate - Wikipedia

    en.wikipedia.org/wiki/Phosphate

    At pH 1 or lower, the phosphoric acid is practically undissociated. Around pH 4.7 (mid-way between the first two pK a values) the dihydrogen phosphate ion, [H 2 PO 4] −, is practically the only species present. Around pH 9.8 (mid-way between the second and third pK a values) the monohydrogen phosphate ion, [HPO 4] 2−, is the only species ...

  6. Pyrophosphate - Wikipedia

    en.wikipedia.org/wiki/Pyrophosphate

    The pKa's occur in two distinct ranges because deprotonations occur on separate phosphate groups. For comparison with the pK a 's for phosphoric acid are 2.14, 7.20, and 12.37. At physiological pH's, pyrophosphate exists as a mixture of doubly and singly protonated forms.

  7. Phosphatidic acid - Wikipedia

    en.wikipedia.org/wiki/Phosphatidic_acid

    By the acylation of lysophosphatidic acid by lysoPA-acyltransferase (LPAAT); this is the most common pathway. [5] The glycerol 3-phosphate pathway for de novo synthesis of PA is shown here: In addition, PA can be converted into DAG by lipid phosphate phosphohydrolases (LPPs) [6] [7] or into lyso-PA by phospholipase A (PLA).

  8. Hypophosphoric acid - Wikipedia

    en.wikipedia.org/wiki/Hypophosphoric_acid

    Hypophosphoric acid can be prepared by the reaction of red phosphorus with sodium chlorite at room temperature. [2]2 P + 2 NaClO 2 + 2 H 2 O → Na 2 H 2 P 2 O 6 + 2 HCl. A mixture of hypophosphoric acid, phosphorous acid (H 3 PO 3) and phosphoric acid (H 3 PO 4) is produced when white phosphorus oxidises in air when partially immersed in water.

  9. Organophosphorus chemistry - Wikipedia

    en.wikipedia.org/wiki/Organophosphorus_chemistry

    Organophosphorus chemistry is the scientific study of the synthesis and properties of organophosphorus compounds, which are organic compounds containing phosphorus. [1] They are used primarily in pest control as an alternative to chlorinated hydrocarbons that persist in the environment.