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  2. N-Methyl-2-pyrrolidone - Wikipedia

    en.wikipedia.org/wiki/N-Methyl-2-pyrrolidone

    N-Methyl-2-pyrrolidone (NMP) is an organic compound consisting of a 5-membered lactam. It is a colorless liquid, although impure samples can appear yellow. It is miscible with water and with most common organic solvents. It also belongs to the class of dipolar aprotic solvents such as dimethylformamide and dimethyl sulfoxide.

  3. BTX (chemistry) - Wikipedia

    en.wikipedia.org/wiki/BTX_(chemistry)

    Many different solvents are suitable, including sulfolane (C 4 H 8 O 2 S), furfural (C 5 H 4 O 2), tetraethylene glycol (C 8 H 18 O 5), dimethylsulfoxide (C 2 H 6 OS), and N-methyl-2-pyrrolidone (C 5 H 9 NO). Below is a schematic flow diagram of one method, involving extractive distillation, for extraction of the BTX aromatics from a catalytic ...

  4. N-Methylmorpholine - Wikipedia

    en.wikipedia.org/wiki/N-Methylmorpholine

    N-Methylmorpholine is the organic compound with the formula O(CH 2 CH 2) 2 NCH 3. It is a colorless liquid. It is a cyclic tertiary amine. It is used as a base catalyst for generation of polyurethanes and other reactions. It is produced by the reaction of methylamine and diethylene glycol as well as by the hydrogenolysis of N-formylmorpholine. [2]

  5. γ-Butyrolactone - Wikipedia

    en.wikipedia.org/wiki/Γ-butyrolactone

    Butyrolactone is a precursor to other chemicals. Reaction with methylamine gives NMP, and with ammonia gives pyrrolidone. It is also used as a solvent in lotions and some polymers. [5] 2-Methyl-4-chlorophenoxybutyric acid is an herbicide produced from butyrolactone.

  6. Butadiene - Wikipedia

    en.wikipedia.org/wiki/Butadiene

    Butadiene is typically isolated from the other four-carbon hydrocarbons produced in steam cracking by extractive distillation using a polar aprotic solvent such as acetonitrile, N-methyl-2-pyrrolidone, furfural, or dimethylformamide, from which it is then stripped by distillation. [15]

  7. Pyrrole - Wikipedia

    en.wikipedia.org/wiki/Pyrrole

    In the cases of N-substituted pyrroles, metalation of the carbons is more facile. Alkyl groups can be introduced as electrophiles, or by cross-coupling reactions. [citation needed] Pyrrole C-metalation. Substitution at C3 can be achieved through the use of N-substituted 3-bromopyrrole, which can be synthesized by bromination of N-silylpyrrole ...

  8. 15 High-Protein Breakfast Ideas That Are So Good You Won't ...

    www.aol.com/15-high-protein-breakfast-ideas...

    Almond-Buckwheat Granola with Yogurt and Berries. Protein per serving: 21 grams Meet the gold standard of high-protein breakfasts: Greek yogurt. The thick and creamy staple has nearly 20 grams per ...

  9. N-methyl pyrrolidone - Wikipedia

    en.wikipedia.org/?title=N-methyl_pyrrolidone&...

    This page was last edited on 12 November 2012, at 01:46 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.