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  2. Trioctylamine - Wikipedia

    en.wikipedia.org/wiki/Trioctylamine

    Trioctylamine is a clear and colorless chemical compound in the group of aliphatic amines and tertiary amines. ... density of 0.810 g/mL at 20 °C; refractive index ...

  3. Triethylamine - Wikipedia

    en.wikipedia.org/wiki/Triethylamine

    Triethylamine is the chemical compound with the formula N(CH 2 CH 3) 3, commonly abbreviated Et 3 N. It is also abbreviated TEA, yet this abbreviation must be used carefully to avoid confusion with triethanolamine or tetraethylammonium, for which TEA is also a common abbreviation.

  4. tert-Butylamine - Wikipedia

    en.wikipedia.org/wiki/Tert-Butylamine

    tert-Butylamine (also erbumine and other names) is an organic chemical compound with the formula (CH 3) 3 CNH 2.It is a colorless liquid with a typical amine-like odor. tert-Butylamine is one of the four isomeric amines of butane, the others being n-butylamine, sec-butylamine and isobutylamine.

  5. Triallylamine - Wikipedia

    en.wikipedia.org/wiki/Triallylamine

    Triallylamine is the organic compound with the formula N(CH 2 CH=CH 2) 3.It is a colorless liquid with an ammonia-like odor. It is multifunctional, featuring a tertiary amine and three alkene groups.

  6. Triethylaluminium - Wikipedia

    en.wikipedia.org/wiki/Triethylaluminium

    Triethylaluminium can be formed via several routes. The discovery of an efficient route was a significant technological achievement. The multistep process uses aluminium, hydrogen gas, and ethylene, summarized as follows: [4]

  7. 2,4,6-Trimethylaniline - Wikipedia

    en.wikipedia.org/wiki/2,4,6-Trimethylaniline

    Trimethylaniline is a building block to a variety of bulky ligands. Condensation with glyoxal gives the 1,2-diimine ligands.An example is glyoxal-bis(mesitylimine), a yellow solid that is synthesized by condensation of 2,4,6-trimethylaniline and glyoxal.

  8. Triethylsilane - Wikipedia

    en.wikipedia.org/wiki/Triethylsilane

    Triethylsilane is the organosilicon compound with the formula (C 2 H 5) 3 SiH. It is a trialkylsilane. The Si-H bond is reactive. It was first discovered by Albert Ladenburg in 1872 among the products of reduction of tetraethyl orthosilicate with sodium and diethylzinc. [2]

  9. 1,1,3,3-Tetramethylguanidine - Wikipedia

    en.wikipedia.org/wiki/1,1,3,3-Tetramethylguanidine

    Density: 918 mg mL −1: Melting point: −30 °C (−22 °F; 243 K) Boiling point: 160 to 162 °C (320 to 324 °F; 433 to 435 K) Solubility in water. Miscible