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  2. 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.

  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. 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.

  6. 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]

  7. Diethyl phosphorochloridate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_phosphorochloridate

    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] The molecule is tetrahedral.

  8. 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.

  9. Category:Phosphate esters - Wikipedia

    en.wikipedia.org/wiki/Category:Phosphate_esters

    Pages in category "Phosphate esters" The following 76 pages are in this category, out of 76 total. ... Tris(1,3-dichloro-2-propyl)phosphate; U. Uridine monophosphate;