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  2. Ethyleneamine - Wikipedia

    en.wikipedia.org/wiki/Ethyleneamine

    A sample of ethylenediamine, a simple ethyleneamine. Ethyleneamines are a class of amine compounds containing ethylene (-CH 2 CH 2-) linkages between amine groups.These compounds are generally colorless, low-viscosity liquids with a fishy amine odor.

  3. Aziridine - Wikipedia

    en.wikipedia.org/wiki/Aziridine

    The bond angles in aziridine are approximately 60°, considerably less than the normal hydrocarbon bond angle of 109.5°, which results in angle strain as in the comparable cyclopropane and ethylene oxide molecules.

  4. Polyethylenimine - Wikipedia

    en.wikipedia.org/wiki/Polyethylenimine

    Polyethylenimine (PEI) or polyaziridine is a polymer with repeating units composed of the amine group and two carbon aliphatic CH 2 CH 2 spacers. Linear polyethyleneimines contain all secondary amines, in contrast to branched PEIs which contain primary, secondary and tertiary amino groups.

  5. Aziridines - Wikipedia

    en.wikipedia.org/wiki/Aziridines

    Mitomycin C, an aziridine, is used as a chemotherapeutic agent by virtue of its antitumour activity. [1]In organic chemistry, aziridines are organic compounds containing the aziridine functional group (chemical structure (R−) 4 C 2 N−R), a three-membered heterocycle with one amine (>NR) and two methylene bridges (>CR 2).

  6. Ethylenediamine - Wikipedia

    en.wikipedia.org/wiki/Ethylenediamine

    Ethylenediamine (abbreviated as en when a ligand) is the organic compound with the formula C 2 H 4 (NH 2) 2.This colorless liquid with an ammonia-like odor is a basic amine.It is a widely used building block in chemical synthesis, with approximately 500,000 tonnes produced in 1998. [6]

  7. Binary ethylenimine - Wikipedia

    en.wikipedia.org/wiki/Binary_ethylenimine

    Binary ethylenimine (BEI) is a preparation of aziridine.It can be produced by heating bromoethylamine hydrobromide or 2-aminoethyl hydrogen sulfate in the presence of sodium hydroxide (Gabriel method).

  8. Wenker synthesis - Wikipedia

    en.wikipedia.org/wiki/Wenker_synthesis

    The Wenker synthesis is an organic reaction converting a beta amino alcohol to an aziridine with the help of sulfuric acid.It is used industrially for the synthesis of aziridine itself.

  9. Immediately dangerous to life or health - Wikipedia

    en.wikipedia.org/wiki/Immediately_dangerous_to...

    Ethyleneimine: 176 mg/m 3: 100 ppm: 151564, carcinogenic substance 75-21-8: 0155: Ethylene oxide: 1440 mg/m 3: 800 ppm: html, carcinogenic substance 60-29-7: 0355 ...