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  2. Amino radical - Wikipedia

    en.wikipedia.org/wiki/Amino_radical

    In chemistry, the amino radical, ·NH2, also known as the aminyl or azanyl, is the neutral form of the amide ion (NH2). Aminyl radicals are highly reactive and consequently short-lived, like most radicals; however, they form an important part of nitrogen chemistry. In sufficiently high concentration, amino radicals dimerise to form hydrazine.

  3. Azanide - Wikipedia

    en.wikipedia.org/wiki/Azanide

    Azanide is the IUPAC -sanctioned name for the anion NH2. The term is obscure; derivatives of NH2 are almost invariably referred to as amides, [1][2][3] despite the fact that amide also refers to the organic functional group – C (=O)−NR2. The anion NH2 is the conjugate base of ammonia, so it is formed by the self-ionization of ...

  4. Amine - Wikipedia

    en.wikipedia.org/wiki/Amine

    Amine. In chemistry, amines (/ ə ˈ m iː n, ˈ æ m iː n /, [1] [2] UK also / ˈ eɪ m iː n / [3]) are compounds and functional groups that contain a basic nitrogen atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group [4] (these may respectively be called alkylamines ...

  5. Hydroxylamine - Wikipedia

    en.wikipedia.org/wiki/Hydroxylamine

    Hydroxylamine (also known as hydroxyammonia) is an inorganic compound with the chemical formula N H 2 O H. The compound is in a form of a white hygroscopic crystals. [4] Hydroxylamine is almost always provided and used as an aqueous solution. It is consumed almost exclusively to produce Nylon-6.

  6. Imide - Wikipedia

    en.wikipedia.org/wiki/Imide

    Imide. In organic chemistry, an imide is a functional group consisting of two acyl groups bound to nitrogen. [1] The compounds are structurally related to acid anhydrides, although imides are more resistant to hydrolysis. In terms of commercial applications, imides are best known as components of high-strength polymers, called polyimides.

  7. Carbamic acid - Wikipedia

    en.wikipedia.org/wiki/Carbamic_acid

    Carbamic acid is a planar molecule. [3]The H 2 N− group of carbamic acid, unlike that of most amines, cannot be protonated to an ammonium group H 3 N + −.The zwitterionic form H 3 N + −COO − is very unstable and promptly decomposes into ammonia and carbon dioxide, [6] yet there is a report of its detection in ices irradiated with high-energy protons.

  8. Aromatic amine - Wikipedia

    en.wikipedia.org/wiki/Aromatic_amine

    Aromatic amine. In organic chemistry, an aromatic amine is an organic compound consisting of an aromatic ring attached to an amine. It is a broad class of compounds that encompasses anilines, but also many more complex aromatic rings and many amine substituents beyond NH2. Such compounds occur widely. [1] Representative aromatic amines.

  9. Ammonium cyanate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_cyanate

    60.056 g·mol −1. Appearance. Colorless crystals. Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references. Ammonium cyanate is an inorganic compound with the formula [NH4]+[OCN]−. It is a colorless, solid salt.