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  2. Organophosphate - Wikipedia

    en.wikipedia.org/wiki/Organophosphate

    Esterifications of phosphoric acid with alcohols proceed less readily than the more common carboxylic acid esterifications, with the reactions rarely proceeding much further than the phosphate mono-ester. The reaction requires high temperatures, under which the phosphoric acid can dehydrate to form poly-phosphoric acids.

  3. Phosphoryl chloride - Wikipedia

    en.wikipedia.org/wiki/Phosphoryl_chloride

    Phosphoryl chloride (commonly called phosphorus oxychloride) is a colourless liquid with the formula P O Cl 3. It hydrolyses in moist air releasing phosphoric acid and fumes of hydrogen chloride. It is manufactured industrially on a large scale from phosphorus trichloride and oxygen or phosphorus pentoxide. [4] It is mainly used to make ...

  4. Diphenylphosphoryl azide - Wikipedia

    en.wikipedia.org/wiki/Diphenylphosphoryl_azide

    Phosphoric acid diphenyl ester azide. Identifiers CAS Number. 26386-88-9 ...

  5. 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 ...

  6. 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 ...

  7. Phosphomonoester - Wikipedia

    en.wikipedia.org/wiki/Phosphomonoester

    Phosphomonoesters (or phosphoric esters) are chemical compounds containing one ester bond and a phosphate group. In biology, phosphomonoesters are needed as the building blocks for the synthesis of Phospholipid cellular membranes, especially those found on neurons. [1] Enzymes which cleave these bonds are known as phosphomonoesterases, or ...

  8. 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.

  9. Tributyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Tributyl_phosphate

    TBP is a solvent and plasticizer for cellulose esters such as nitrocellulose and cellulose acetate, similarly to tricresyl phosphate. It is also used as a flame retardant for cellulose fabrics such as cotton. [7] [8] It forms stable hydrophobic complexes with some metals; these complexes are soluble in organic solvents as well as supercritical ...