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  2. 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]

  3. Phosphoric acids and phosphates - Wikipedia

    en.wikipedia.org/.../Phosphoric_acids_and_phosphates

    See the general structure image of an ortho- (or mono-) phosphate ester below on the left, where any of the R groups can be a hydrogen or an organic radical. Di- and tripoly- (or tri-) phosphate esters, etc. are also possible.

  4. 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 ...

  5. Triphenyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Triphenyl_phosphate

    Triphenyl phosphate (TPhP) is the chemical compound with the formula OP(OC 6 H 5) 3. It is the simplest aromatic organophosphate. This colourless solid is the ester (triester) of phosphoric acid and phenol. It is used as a plasticizer and a fire retardant in a wide variety of settings and products. [3]

  6. Skydrol - Wikipedia

    en.wikipedia.org/wiki/Skydrol

    It is a phosphate ester-based fluid that is known for its excellent fire resistance and ability to withstand extreme temperature and pressure conditions. It is manufactured by Solutia (now part of Eastman Chemical Company), and formerly manufactured by Monsanto. There are various lines of Skydrol including Skydrol 500B-4, Skydrol LD-4, and ...

  7. Diethyl phosphorochloridate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_phosphorochloridate

    Diethyl chlorophosphate is an organophosphorus compound with the formula (C 2 H 5 O) 2 P(O)Cl. As a reagent in organic synthesis, it is used to convert alcohols to the corresponding diethylphosphate esters. It is a colorless liquid with a fruity odor. It is a corrosive, and as a cholinesterase inhibitor, highly toxic through dermal absorption. [1]

  8. Phosphate ester - Wikipedia

    en.wikipedia.org/?title=Phosphate_ester&redirect=no

    Phosphate ester. Add languages. Add links. ... Upload file; Special pages; ... Get shortened URL; Download QR code; Print/export Download as PDF; Printable version ...

  9. Category:Phosphate esters - Wikipedia

    en.wikipedia.org/wiki/Category:Phosphate_esters

    Testosterone phosphate; THC-O-phosphate; Thiamine triphosphate; Thymidine monophosphate; Thymidine triphosphate; Tributyl phosphate; Tricresyl phosphate; Triethyl phosphate; Trimethyl phosphate; Triphenyl phosphate; Tris(1,3-dichloro-2-propyl)phosphate