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  2. Phosphite ester - Wikipedia

    en.wikipedia.org/wiki/Phosphite_ester

    Phosphite esters may be used as reducing agents in more specialised cases. For example, triethylphosphite is known to reduce certain hydroperoxides to alcohols formed by autoxidation [7] (scheme). In this process the phosphite is converted to a phosphate ester. This reaction type is also utilized in the Wender Taxol total synthesis.

  3. Organophosphate - Wikipedia

    en.wikipedia.org/wiki/Organophosphate

    These are primarily the esters of phosphoric acid and can be mono‑esters, di‑esters or tri‑esters depending on the number of attached organic groups (abbreviated as 'R' in the image below). In general man‑made organophosphates are most often triesters, while biological organophosphates are usually mono- or di-esters.

  4. Phosphoric acids and phosphates - Wikipedia

    en.wikipedia.org/.../Phosphoric_acids_and_phosphates

    Likewise, tripolyphosphoric acid H 5 P 3 O 10 yields at least five anions [H 5−k P 3 O 10] k−, where k ranges from 1 to 5, including tripolyphosphate [P 3 O 10] 5−. Tetrapolyphosphoric acid H 6 P 4 O 13 yields at least six anions, including tetrapolyphosphate [P 4 O 13] 6−, and so on. Note that each extra phosphoric unit adds one extra ...

  5. Trixylyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Trixylyl_phosphate

    Trixylyl phosphate (TXP) is an aromatic phosphate ester. It was historically used as a flame retardant for acetate plastics (cellulose nitrate and cellulose acetate) and PVC. It also saw significant use as a fire-resistant hydraulic fluid. Trixylyl phosphate is now banned or restricted in several jurisdictions, due to its poor safety profile.

  6. Di(2-ethylhexyl)phosphoric acid - Wikipedia

    en.wikipedia.org/wiki/Di(2-ethylhexyl)phosphoric...

    Di(2-ethylhexyl)phosphoric acid (DEHPA or HDEHP) is an organophosphorus compound with the formula (C 8 H 17 O) 2 PO 2 H. The colorless liquid is a diester of phosphoric acid and 2-ethylhexanol . It is used in the solvent extraction of uranium , vanadium and the rare-earth metals .

  7. Organophosphorus chemistry - Wikipedia

    en.wikipedia.org/wiki/Organophosphorus_chemistry

    Phosphate esters have the general structure P(=O)(OR) 3 feature P(V). Such species are of technological importance as flame retardant agents, and plasticizers. Lacking a P−C bond, these compounds are in the technical sense not organophosphorus compounds but esters of phosphoric acid. Many derivatives are found in nature, such as ...

  8. Trimethyl phosphite - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_phosphite

    Trimethyl phosphite is an organophosphorus compound with the formula P(OCH 3) 3, often abbreviated P(OMe) 3.It is a colorless liquid with a highly pungent odor. It is the simplest phosphite ester and finds used as a ligand in organometallic chemistry and as a reagent in organic synthesis.

  9. 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 ...