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  2. Trimethyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_phosphate

    Trimethyl phosphate is prepared by treating phosphorus oxychloride with methanol in the presence of an amine base: POCl 3 + 3 CH 3 OH + 3 R 3 N → PO(OCH 3 ) 3 + 3 R 3 NH + Cl − It is a tetrahedral molecule that is a weakly polar solvent.

  3. Triple Super Phosphate Complex Limited - Wikipedia

    en.wikipedia.org/wiki/Triple_Super_Phosphate...

    It was founded by East Pakistan Industrial Development Corporation (EPIDC) before the independence of Bangladesh and went into commercial production in 1974. [4] Among the units TSP-II was commissioned earlier in September 1974 and TSP-I unit went into commercial production in April 1977.

  4. File:Detergent Phosphate Ban Position Paper USEPA.pdf

    en.wikipedia.org/wiki/File:Detergent_Phosphate...

    Original file (1,266 × 1,772 pixels, file size: 2.87 MB, MIME type: application/pdf, 67 pages) This is a file from the Wikimedia Commons . Information from its description page there is shown below.

  5. Dimethyl methylphosphonate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_methylphosphonate

    Dimethyl methylphosphonate can be prepared from trimethyl phosphite and a halomethane (e.g. iodomethane) via the Michaelis–Arbuzov reaction. [2]Dimethyl methylphosphonate is a schedule 2 chemical as it may be used in the production of chemical weapons.

  6. Dichlorvos - Wikipedia

    en.wikipedia.org/wiki/Dichlorvos

    Dichlorvos (2,2-dichlorovinyl dimethyl phosphate, commonly abbreviated as an DDVP [1]) is an organophosphate widely used as an insecticide to control household pests, in public health, and protecting stored products from insects. The compound has been commercially available since 1961.

  7. Phosphite ester - Wikipedia

    en.wikipedia.org/wiki/Phosphite_ester

    Phosphites are oxidized to phosphate esters: P(OR) 3 + [O] → OP(OR) 3. This reaction underpins the commercial use of some phosphite esters as stabilizers in polymers. [6] Alkyl phosphite esters are used in the Perkow reaction for the formation of vinyl phosphonates, and in the Michaelis–Arbuzov reaction to form phosphonates.

  8. Trimethylphosphine - Wikipedia

    en.wikipedia.org/wiki/Trimethylphosphine

    Trimethylphosphine is a highly basic ligand that forms complexes with most metals. As a ligand, trimethylphosphine's Tolman cone angle is 118°. [7] This angle is an indication of the amount of steric protection that this ligand provides to the metal that to which it is bound.

  9. Trimethyl phosphite - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_phosphite

    As a ligand, trimethyl phosphite has a smaller cone angle and better acceptor properties relative to trimethylphosphine. A representative derivative is the colorless tetrahedral complex Ni(P(OMe) 3) 4 (m.p. 108 °C). [4] The tridentate ligand called the Kläui ligand is derived from trimethyl phosphite. The formation of this ligand illustrates ...