enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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

    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.

  4. Triple Super Phosphate Complex Limited - Wikipedia

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

    Among the units TSP-II was commissioned earlier in September 1974 and TSP-I unit went into commercial production in April 1977. In the beginning it only produced Triple Super Phosphate (TSP) fertilizer and from 1990 is started producing Single superphosphate fertilizer also. The fertilizer complex is located Karnaphuli river bank at Patenga ...

  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. Triethyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Triethyl_phosphate

    Triethyl phosphate is an organic chemical compound with the formula (C 2 H 5) 3 PO 4 or OP(OEt) 3. It is a colorless liquid. It is a colorless liquid. It is the triester of ethanol and phosphoric acid and can be called "phosphoric acid, triethyl ester".

  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. Acme Laboratories - Wikipedia

    en.wikipedia.org/wiki/ACME_Laboratories

    1954 Year of the establishment (initially as a partnership) 1976 The firm was converted into a private limited company; 1983 Commercial operation at the modernized plant equipped with sophisticated and advanced facilities

  9. Phosphorus trichloride - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_trichloride

    For example, oxidation of PCl 3 gives POCl 3, which is used for the manufacture of triphenyl phosphate and tricresyl phosphate, which find application as flame retardants and plasticisers for PVC. They are also used to make insecticides such as diazinon. Phosphonates include the herbicide glyphosate.