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  2. Category:Tertiary amines - Wikipedia

    en.wikipedia.org/wiki/Category:Tertiary_amines

    Pages in category "Tertiary amines" The following 96 pages are in this category, out of 96 total. This list may not reflect recent changes. 0–9. 1P-AL-LAD;

  3. ATC code A03 - Wikipedia

    en.wikipedia.org/wiki/ATC_code_A03

    ATC code A03 Drugs for functional gastrointestinal disorders is a therapeutic subgroup of the Anatomical Therapeutic Chemical Classification System, a system of alphanumeric codes developed by the World Health Organization (WHO) for the classification of drugs and other medical products.

  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(NH 3 (in which the bond angle between the nitrogen and hydrogen is 107°), wherein one or more hydrogen atoms have been replaced by a substituent such as an ...

  5. Aminoaldehydes and aminoketones - Wikipedia

    en.wikipedia.org/wiki/Aminoaldehydes_and_aminoke...

    Because primary and secondary amines react with aldehydes and ketones, the most common variety of these aminocarbonyl compounds feature tertiary amines. Such compounds are produced by amination of α-haloketones and α-haloaldehydes. [1] Examples include cathinones, methadone, molindone, pimeclone, ferruginine, and tropinone.

  6. Amine alkylation - Wikipedia

    en.wikipedia.org/wiki/Amine_alkylation

    For example, reaction of 1-bromooctane with ammonia yields almost equal amounts of the primary amine and the secondary amine. [3] Therefore, for laboratory purposes, N-alkylation is often limited to the synthesis of tertiary amines. An exception is the amination of alpha-halo carboxylic acids that do permit synthesis of primary amines with ...

  7. List of local anesthetics - Wikipedia

    en.wikipedia.org/wiki/List_of_local_anesthetics

    Drug Other common names Image First synthesis Dates of clinical use Chemical/structural class Duration of effect amylocaine: Stovaine 1904 (Ernest Fourneau) ester- benzoic ambucaine [1] diester - aminosalicylic articaine: Astracaine, Septanest, Septocaine, Ultracaine, Zorcaine Amide benzocaine: Anbesol, Orajel Ester - Aminobenzoic Short benzonatate

  8. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    Halide-containing compounds are pervasive, making this type of transformation important, e.g. in the production of polymers, drugs. [1] This kind of conversion is in fact so common that a comprehensive overview is challenging. This article mainly deals with halogenation using elemental halogens (F 2, Cl 2, Br 2, I 2). Halides are also commonly ...

  9. Alkanolamine - Wikipedia

    en.wikipedia.org/wiki/Alkanolamine

    Examples include prolinol (from proline), valinol (from valine), tyrosinol (from tyrosine). Key members: ethanolamine , dimethylethanolamine , N -methylethanolamine , Aminomethyl propanol . Two popular drugs, often called alkanolamine beta blockers , are members of this structural class: propranolol , pindolol .