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3.5: Chemical Properties of Amines. Bases and Salt Formation.

  • Page ID
    227545
  • Learning Objectives

    • Name the typical reactions that take place with amines.
    • Describe heterocyclic amines.

    The main chemical property of amines is their ability to act as weak organic bases. Recall that ammonia (NH3) acts as a base because the nitrogen atom has a lone pair of electrons that can accept a proton. Amines also have a lone electron pair on their nitrogen atoms and can accept a proton from water to form substituted ammonium (NH4+) ions and hydroxide (OH) ions:

    ammonium.jpg

    As a specific example, methylamine reacts with water to form the methylammonium ion and the OH ion.

    methylammonium ion.jpg

    The Kb value for methylamine is 4.6 × 10−4

    Since they are bases,  amines will react with acids to form salts soluble in water, including those amines that are not very soluble in water:

    soluble.jpg

    Amine salts are named like other salts: the name of the cation is followed by the name of the anion. In the name for the cation, we change “amine” to “ammonium”.

    Example \(\PageIndex{1}\)

    What are the formulas of the acid and base that react to form [CH3NH2CH2CH3]+CH3COO? What is the name of the salt

    Solution

    The cation has two groups—methyl and ethyl—attached to the nitrogen atom. It comes from ethylmethylamine (CH3NHCH2CH3). The anion is the acetate ion. It comes from acetic acid (CH3COOH).

    The name of the salts is ehtylmethylammonium ethanoate (IUPAC name) or ehtylmethylammonium acetate (common name

     

    Ammonium Salt Formation and Water Solubility

    Many pharmaceuticals include amine functional groups. Sometimes the basicity of these amine groups is used to increase the water solubility of a drug so that it can be administered orally or intravenously. Ammonium salts are also thermally more stable and have less odor than their "free base" conjugates. The antihistamine, pseudoephedrine, reacts with hydrochloric acid to form the water-soluble ammonium salt as shown below.

    ch 20 sect 2 example 1.png

     

    Heterocyclic Amines

    Looking back at the various cyclic hydrocarbons discussed previously, we see that all the atoms in the rings of these compounds are carbon atoms. In other cyclic compounds, called heterocyclic compounds (Greek heteros, meaning “other”), nitrogen, oxygen, sulfur, or some other atom is incorporated in the ring. Many heterocyclic compounds are important in medicine and biochemistry. Some compose part of the structure of the nucleic acids, which in turn compose the genetic material of cells and direct protein synthesis.

    Many heterocyclic amines occur naturally in plants. Like other amines, these compounds are basic. Such a compound is an alkaloid, a name that means “like alkalis.” Many alkaloids are physiologically active, including the familiar drugs caffeine, nicotine, and cocaine.

    To Your Health: Three Well-Known Alkaloids

    Caffeine is a stimulant found in coffee, tea, and some soft drinks. Its mechanism of action is not well understood, but it is thought to block the activity of adenosine, a heterocyclic base that acts as a neurotransmitter, a substance that carries messages across a tiny gap (synapse) from one nerve cell (neuron) to another cell. The effective dose of caffeine is about 200 mg, corresponding to about two cups of strong coffee or tea.

    caffeine.jpg

    Nicotine acts as a stimulant by a different mechanism; it probably mimics the action of the neurotransmitter acetylcholine. People ingest this drug by smoking or chewing tobacco. Its stimulant effect seems transient, as this initial response is followed by depression. Nicotine is highly toxic to animals. It is especially deadly when injected; the lethal dose for a human is estimated to be about 50 mg. Nicotine has also been used in agriculture as a contact insecticide.

    nicotine.jpg

    Cocaine acts as a stimulant by preventing nerve cells from taking up dopamine, another neurotransmitter, from the synapse. High levels of dopamine are therefore available to stimulate the pleasure centers of the brain. The enhancement of dopamine action is thought to be responsible for cocaine’s “high” and its addictive properties. After the binge, dopamine is depleted in less than an hour. This leaves the user in a pleasureless state and (often) craving more cocaine.

    cocaine.jpg

    Cocaine is used as the salt cocaine hydrochloride and in the form of broken lumps of the free (unneutralized) base, which is called crack cocaine.

    cocaine hydrochloride.jpg

    Because it is soluble in water, cocaine hydrochloride is readily absorbed through the watery mucous membranes of the nose when it is snorted. Crack cocaine is more volatile than cocaine hydrochloride. It vaporizes at the temperature of a burning cigarette. When smoked, cocaine reaches the brain in 15 s.

    Summary

    Amines are bases; they react with acids to form salts. Salts of aniline are properly named as ammonium compounds. Heterocyclic amines are cyclic compounds with one or more nitrogen atoms in the ring.

    Concept Review Exercises

    1. Explain the basicity of amines.
    2. Contrast the physical properties of amines with those of alcohols and alkanes.
    3. What is a cyclic amine?

    Answers

    1. Amines have a lone pair of electrons on the nitrogen atom and can thus act as proton acceptors (bases).
    2. The solubilities of amines are similar to those of alcohols; the boiling points of primary and secondary amines are similar to those of alcohols; the boiling points of tertiary amines, which cannot engage in hydrogen bonding because they do not have a hydrogen atom on the nitrogen atom, are comparable to those of alkanes.
    3. Cyclic amines are ring compounds with nitrogen atoms in the ring.

    Exercises

    1. What salt is formed in each reaction? Write its condensed structural formula and its name.

      1. CH3NH2(aq) + HBr(aq) →
      2. CH3NHCH3(aq) + HNO3(aq) →
    2. What salt is formed in each reaction? Draw its structure.

      1. 2a.jpg
      2. 2b.jpg

    Answer

      1. CH3NH3+Br(aq) methylammonium bromide
      2. [CH3NH2CH3]+NO3(aq) dimethylammonium nitrate

       

      Contributors and Attributions

       

      Dr. Dietmar Kennepohl FCIC (Professor of Chemistry, Athabasca University)

      Prof. Steven Farmer (Sonoma State University)

      William Reusch, Professor Emeritus (Michigan State U.), Virtual Textbook of Organic Chemistry

      Organic Chemistry With a Biological Emphasis by Tim Soderberg (University of Minnesota, Morris)

      Amines as Bases. (2020, August 17). Retrieved May 23, 2021, from https://chem.libretexts.org/@go/page/16035

       

       

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