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  2. 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 ...

  3. Organophosphate - Wikipedia

    en.wikipedia.org/wiki/Organophosphate

    General chemical structure of the organophosphate functional group. In organic chemistry, organophosphates (also known as phosphate esters, or OPEs) are a class of organophosphorus compounds with the general structure O=P(OR) 3, a central phosphate molecule with alkyl or aromatic substituents. [1]

  4. Phosphoryl chloride - Wikipedia

    en.wikipedia.org/wiki/Phosphoryl_chloride

    Phosphoryl chloride is used on an industrial scale for the manufacture of phosphate esters (organophosphates). These have a wide range of uses, including as flame retardants (bisphenol A diphenyl phosphate, TCPP and tricresyl phosphate), plasticisers for PVC and related polymers (2-ethylhexyl diphenyl phosphate) and hydraulic fluids. [11]

  5. Phosphoric acids and phosphates - Wikipedia

    en.wikipedia.org/.../Phosphoric_acids_and_phosphates

    Sometimes pyrophosphate, tripolyphosphate, tetrapolyphosphate, etc. are called diphosphate, triphosphate, tetraphosphate, etc., especially when they are part of phosphate esters in biochemistry. They are also used for scale and corrosion control by potable water providers . [ 6 ]

  6. 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.

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

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

    Compared to phosphate extractants, amines are more selective for uranium, extract the uranium faster, and are easily stripped with a wider variety of reagents. However, the phosphates are more tolerant of solids in the feed solution and show faster phase separation.

  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. Tributyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Tributyl_phosphate

    Tributyl phosphate, known commonly as TBP, is an organophosphorus compound with the chemical formula (CH 3 CH 2 CH 2 CH 2 O) 3 PO. This colourless, odorless liquid finds some applications as an extractant and a plasticizer. It is an ester of phosphoric acid with n-butanol.