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  2. Nitrile - Wikipedia

    en.wikipedia.org/wiki/Nitrile

    The structure of a nitrile: the functional group is highlighted blue. In organic chemistry, a nitrile is any organic compound that has a −C≡N functional group.The name of the compound is composed of a base, which includes the carbon of the −C≡N, suffixed with "nitrile", so for example CH 3 CH 2 C≡N is called "propionitrile" (or propanenitrile). [1]

  3. Nitrile rubber - Wikipedia

    en.wikipedia.org/wiki/Nitrile_rubber

    Nitrile rubber, also known as nitrile butadiene rubber, NBR, Buna-N, and acrylonitrile butadiene rubber, is a synthetic rubber derived from acrylonitrile (ACN) and butadiene. [1] Trade names include Perbunan, Nipol, Krynac and Europrene. This rubber is unusual in being resistant to oil, fuel, and other chemicals.

  4. Nitrile reduction - Wikipedia

    en.wikipedia.org/wiki/Nitrile_reduction

    The mechanism for the reduction of a nitrile to an aldehyde with DIBAL-H. The hydride reagent Diisobutylaluminium hydride, or DIBAL-H, is commonly used to convert nitriles to the aldehyde. [14] Regarding the proposed mechanism, DIBAL forms a Lewis acid-base adduct with the nitrile by formation of an N-Al bond. The hydride is then transferred to ...

  5. Nitrile anion - Wikipedia

    en.wikipedia.org/wiki/Nitrile_anion

    Nitrile anions is jargon from the organic product resulting from the deprotonation of alkylnitriles. The proton(s) α to the nitrile group are sufficiently acidic that they undergo deprotonation by strong bases, usually lithium-derived.

  6. Nitrilase - Wikipedia

    en.wikipedia.org/wiki/Nitrilase

    Nitrilase was first discovered in the early 1960s for its ability to catalyze the hydration of a nitrile to a carboxylic acid. [2] Although it was known at the time that nitrilase could operate with wide substrate specificity in producing the corresponding acid, later studies reported the first NHase (nitrile hydratase) activity exhibited by nitrilase.

  7. Ritter reaction - Wikipedia

    en.wikipedia.org/wiki/Ritter_reaction

    The Ritter reaction (sometimes called the Ritter amidation) is a chemical reaction that transforms a nitrile into an N-alkyl amide using various electrophilic alkylating reagents. The original reaction formed the alkylating agent using an alkene in the presence of a strong acid. [1] [2] [3] [4]

  8. Medical glove - Wikipedia

    en.wikipedia.org/wiki/Medical_glove

    Dentist wearing nitrile gloves Medical gloves are disposable gloves used during medical examinations and procedures to help prevent cross-contamination between caregivers and patients. [ 1 ] Medical gloves are made of different polymers including latex , nitrile rubber , polyvinyl chloride and neoprene ; they come unpowdered, or powdered with ...

  9. Malononitrile - Wikipedia

    en.wikipedia.org/wiki/Malononitrile

    Malononitrile is an organic compound nitrile with the formula CH 2 (CN) 2. It is a colorless or white solid, although aged samples appear yellow or even brown. It is a widely used building block in organic synthesis.