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  2. Trimethyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_phosphate

    Trimethyl phosphate is a mild methylating agent, useful for dimethylation of anilines and related heterocyclic compounds. [2] The method is complementary to the traditional Eschweiler-Clarke reaction in cases where formaldehyde engages in side reactions.

  3. 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 ...

  4. Triple Super Phosphate Complex Limited - Wikipedia

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

    It is under supervision of Bangladesh Chemical Industries Corporation (BCIC). It primarily produces phosphate fertilizers . [ 1 ] [ 2 ] The factory complex consists of 2 units of TSP fertilizer producing facility with installed capacity of 1,52,000 MT (Unit-1; 32,000 MT and Unit-2; 1,20,000 MT).

  5. 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.

  6. Tris(trimethylsilyl)phosphine - Wikipedia

    en.wikipedia.org/wiki/Tris(trimethylsilyl)phosphine

    Tris(trimethylsilyl)phosphine is prepared by treating trimethylsilyl chloride, white phosphorus, and sodium-potassium alloy: [2] 1/4 P 4 + 3 Me 3 SiCl + 3 K → P(SiMe 3) 3 + 3 KCl

  7. 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.

  8. 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.

  9. Triethyl phosphite - Wikipedia

    en.wikipedia.org/wiki/Triethyl_phosphite

    Triethyl phosphite (TEP) is an organophosphorus compound, specifically a phosphite ester, with the formula P(OCH 2 CH 3) 3, often abbreviated P(OEt) 3.It is a colorless, malodorous liquid.