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  2. Diethylamine - Wikipedia

    en.wikipedia.org/wiki/Diethylamine

    Diethylamine is an organic compound with the formula (CH 3 CH 2) 2 NH. It is classified as a secondary amine. It is a flammable, volatile weakly alkaline liquid that is miscible with most solvents. It is a colorless liquid, but commercial samples often appear brown due to impurities. It has a strong ammonia-like odor.

  3. Diethylethanolamine - Wikipedia

    en.wikipedia.org/wiki/Diethylethanolamine

    Diethylethanolamine is an irritant to the eyes, skin, and respiratory system. The Occupational Safety and Health Administration and the National Institute for Occupational Safety and Health have set occupational exposure limits for workers handling the chemical at 10 ppm (50 mg/m 3) over an eight-hour workday.

  4. N,N-Diethylmethylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-diethylmethylamine

    N,N-Diethylmethylamine (diethylmethylamine, DEMA) is a tertiary amine with the formula C 5 H 13 N. N,N-Diethylmethylamine is a clear, colorless to pale yellow liquid at room temperature, and is used in various industrial and scientific applications including water desalination as well as analytical and organic chemistry.

  5. Transition metal dithiocarbamate complexes - Wikipedia

    en.wikipedia.org/wiki/Transition_metal...

    A wide variety of secondary amines give the corresponding dtc ligand. Popular amines include dimethylamine (Me 2 NH), diethylamine (Et 2 NH), and pyrrolidine ((CH 2) 4 NH). Related ligands. Dithiocarbamates are classified as derivatives of dithiocarbamic acid. Their properties as ligands resemble the conjugate bases of many related "1,1 ...

  6. Diethylaniline - Wikipedia

    en.wikipedia.org/wiki/Diethylaniline

    Its condensation with half an equivalent of benzaldehyde gives brilliant green, an analogue of the very useful malachite green.With formylbenzenedisulfonic acid it condenses to give Patent blue VE, and with hydroxybenzaldehyde followed by sulfonation one obtains Patent blue V.

  7. N,N-Diisopropylethylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-Diisopropylethylamine

    DIPEA is a sterically hindered organic base that is commonly employed as a proton scavenger. Thus, like 2,2,6,6-tetramethylpiperidine and triethylamine, DIPEA is a good base but a poor nucleophile, DIPEA has low solubility in water, which makes it very easily recovered in commercial processes, a combination of properties that makes it a useful organic reagent.

  8. Diethylaminoethyl cellulose - Wikipedia

    en.wikipedia.org/wiki/Diethylaminoethyl_cellulose

    Schematic structure of DEAE-C: positively charged diethylaminoethanol groups can bind negative ions. Diethylaminoethyl cellulose (DEAE-C) is a positively charged resin used in ion-exchange chromatography, a type of column chromatography, for the separation and purification of proteins and nucleic acids.

  9. N,N-Dimethylethylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-Dimethylethylamine

    N,N-Dimethylethylamine (DMEA), sometimes referred to as dimethylethylamine, is an organic compound with formula (CH 3) 2 NC 2 H 5.It is an industrial chemical that is mainly used in foundries as a catalyst for epoxy resins and polyurethane as well as sand core production.