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  2. 2-Pyrrolidone - Wikipedia

    en.wikipedia.org/wiki/2-Pyrrolidone

    2-Pyrrolidone is produced industrially almost exclusively by treating aqueous gamma-butyrolactone with ammonia at a temperature of 250–290 °C and pressures ranging from 0.41.4 MPa over solid magnesium silicate catalysts. [3] The reaction is carried out in a tubular reactor which is packed with the solid catalyst. The latter is arranged as ...

  3. N-Vinylpyrrolidone - Wikipedia

    en.wikipedia.org/wiki/N-Vinylpyrrolidone

    It is produced industrially by vinylation of 2-pyrrolidone, i.e. the base-catalyzed reaction with acetylene. [2] It is the precursor to polyvinylpyrrolidone (PVP), an important synthetic material. The NVP monomer is commonly used as a reactive diluent in ultraviolet and electron - beam curable polymers applied as inks , coatings or adhesives .

  4. Polyvinylpyrrolidone - Wikipedia

    en.wikipedia.org/wiki/Polyvinylpyrrolidone

    Polyvinylpyrrolidone (PVP), also commonly called polyvidone or povidone, is a water-soluble polymer compound made from the monomer N-vinylpyrrolidone. [1] PVP is available in a range of molecular weights and related viscosities, and can be selected according to the desired application properties.

  5. Pyrrolidine alkaloids - Wikipedia

    en.wikipedia.org/wiki/Pyrrolidine_alkaloids

    Among the most important representatives of the pyrrolidine alkaloids are hygrin and cuscohygrin. [2] Another representative is the (-)- codonopsinine . [ 3 ] Furthermore, ruspolinone , norruspolinone and norruspoline also belong to this alkaloid group.

  6. Pyrrolidine - Wikipedia

    en.wikipedia.org/wiki/Pyrrolidine

    Pyrrolidine, also known as tetrahydropyrrole, is an organic compound with the molecular formula (CH 2) 4 NH. It is a cyclic secondary amine , also classified as a saturated heterocycle . It is a colourless liquid that is miscible with water and most organic solvents.

  7. N-Methyl-2-pyrrolidone - Wikipedia

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

    N-Methyl-2-pyrrolidone (NMP) is classified as a reproductive toxicant (H360D: May damage the unborn child) and can cause skin and eye irritation and respiratory irritation (H315, H319, H335). [5] Studies show NMP exposure can increase the risk of developmental toxicity, including miscarriage and fetal death. [ 6 ]

  8. Vinyl group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_group

    In organic chemistry, a vinyl group (abbr. Vi; [1] IUPAC name: ethenyl group [2]) is a functional group with the formula −CH=CH 2. It is the ethylene (IUPAC name: ethene) molecule (H 2 C=CH 2) with one fewer hydrogen atom. The name is also used for any compound containing that group, namely R−CH=CH 2 where R is any other group of atoms.

  9. Polyvinylpolypyrrolidone - Wikipedia

    en.wikipedia.org/wiki/Polyvinylpolypyrrolidone

    Polyvinylpolypyrrolidone (polyvinyl polypyrrolidone, PVPP, crospovidone, crospolividone, or E1202) is a highly cross-linked modification of polyvinylpyrrolidone (PVP).. The cross-linked form of PVP is used as a disintegrant (see also excipients) in pharmaceutical tablets. [1]