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  2. 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atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group [4] (these may respectively be called alkylamines ...

  3. Amino acid - Wikipedia

    en.wikipedia.org/wiki/Amino_acid

    Amino acid. Structure of a typical L -alpha-amino acid in the "neutral" form. Amino acids are organic compounds that contain both amino and carboxylic acid functional groups. [1] Although over 500 amino acids exist in nature, by far the most important are the 22 α-amino acids incorporated into proteins. [2]

  4. Ethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylamine

    Ethylamine, also known as ethanamine, is an organic compound with the formula CH 3 CH 2 NH 2. This colourless gas has a strong ammonia -like odor. It condenses just below room temperature to a liquid miscible with virtually all solvents. It is a nucleophilic base, as is typical for amines.

  5. Amide - Wikipedia

    en.wikipedia.org/wiki/Amide

    Asparagine (zwitterionic form), an amino acid with a side chain (highlighted) containing an amide group. In organic chemistry, an amide, [1][2][3] also known as an organic amide or a carboxamide, is a compound with the general formula R−C (=O)−NR′R″, where R, R', and R″ represent any group, typically organyl groups or hydrogen atoms ...

  6. 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 (NH− 2). 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.

  7. Amidine - Wikipedia

    en.wikipedia.org/wiki/Amidine

    Amidine. The skeletal formula of acetamidine (acetimidamide). Amidines are organic compounds with the functional group RC (NR)NR 2, where the R groups can be the same or different. They are the imine derivatives of amides (RC (O)NR 2). The simplest amidine is formamidine, HC (=NH)NH 2. Examples of amidines include:

  8. Cyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylamine

    Cyclohexylamine is used as an intermediate in synthesis of other organic compounds. It is the precursor to sulfenamide -based reagents used as accelerators for vulcanization. The amine itself is an effective corrosion inhibitor. It has been used as a flushing aid in the printing ink industry. [5]

  9. Amine value - Wikipedia

    en.wikipedia.org/wiki/Amine_value

    Amine value. In organic chemistry, amine value is a measure of the nitrogen content of an organic molecule. [1] Specifically, it is usually used to measure the amine content of amine functional compounds. [2] It may be defined as the number of milligrams of potassium hydroxide (KOH) equivalent to one gram of epoxy hardener resin.