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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 ...
In chemistry, a phosphate is an anion, salt, functional group or ester derived from a phosphoric acid. It most commonly means orthophosphate, a derivative of orthophosphoric acid, a.k.a. phosphoric acid H 3 PO 4. The phosphate or orthophosphate ion [PO 4] 3− is derived from phosphoric acid by the removal of three protons H +.
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. It is a major industrial ...
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. Organic derivatives of phosphorous acid, compounds with the ...
Trimetaphosphoric acid (or cyclotriphosphoric acid), H 3 P 3 O 9 (or (HPO 3) 3, (–P(O)(OH)–O–) 3), a cyclic molecule with three acidic hydrogens. Forms the trimetaphosphate salts and esters. Metaphosphoric acid is a general term for phosphoric acids with a single cycle, (–P(O)(OH)–O–) n, whose elemental formula is HPO 3.
Phosphogypsum is a by-product from the production of phosphoric acid by treating phosphate ore with sulfuric acid according to the following reaction: Ca 5 (PO 4) 3 X + 5 H 2 SO 4 + 10 H 2 O → 3 H 3 PO 4 + 5 (CaSO 4 · 2 H 2 O) + HX where X may include OH, F, Cl, or Br
Most processes begin with phosphorous acid (aka phosphonic acid, H 3 PO 3), exploiting its reactive P−H bond. [1] [3]Phosphonic acid can be alkylated via the Kabachnik–Fields reaction or Pudovik reaction to give aminophosphonate, which are useful as chelating agents.
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).