Small molecules make scents

Classroom activity: Experiment 1 Image courtesy of Angelika Börsch-Haubold

Angelika Börsch-Haubold demonstrates the olfactory delights of organic chemistry. “Chemistry is all bangs and smells.” Not all students of chemistry are drawn to the stenches and explosions in the laboratory. Fortunately, there are many organic molecules that actually smell nice. We experience these substances daily – using a perfumed shower gel, flavouring our meals with herbs, or burying our nose deep in a rose. Teaching the organic chemistry of natural scents should motivate even those who despise the toxic and dangerous side of chemistry to look at structural formulae and functionalities. In order to be perceptible by our noses, chemicals need to be lipophilic, small (molecular weight < 300 Da) and volatile. Fragrant molecules escape from their fluid or even solid state into the air.

The sensory tissue, called olfactory epithelium, is a mucous membrane which lies on the roof of the nasal cavity. Odorants reach this area (approximately 7 cm away from the nostrils) in the air we breathe; if something smells very faintly, we sniff two or three more times, forcing more air and fragrance towards the sensory membrane. There, the molecules dissolve in the mucous and then couple to smell receptors that are expressed on the plasma membrane of sensory cells. The cells send nerve impulses to our brain, which learns to associate the smell with the original substance (such as a rose), lets us recognise it even when the object is hidden (such as when entering a house and knowing that a cake is in the oven) or classifies it as unknown (such as when we go to an exotic restaurant for the first time).

Similar chemical properties – similar smells

Arranging smells into a limited number of distinct classes is not as easy as defining the basic tastes (sweet, sour, salty, and bitter). Typical smell attributes are flowery (jasmine), spicy (ginger, pepper), fruity (ethyl acetate), resinous (resin smoke), foul (rotten egg), and burning (tar). Musk (muscone), camphor, rancid (isovaleric acid, butyric acid) and pungent (formic acid, acetic acid) are often added to this list. By concentrating more on chemical details, functional groups of fragrant molecules can be linked to characteristic odours (Table 1). The smells of n-aliphatic alcohols, for example, range from herbal, rose and woody to orange. By contrast, n-aliphatic acids smell fatty, sour, rancid or sweaty. Fruit scents are esters composed of short aliphatic organic acids with alcohols. Subtle differences in the chemical composition lead to distinct scents, such as the pineapple aroma of ethyl butyrate and the apricot aroma of pentyl butyrate. Vegetable smells often depend on organosulphur compounds. A ring structure with nitrogen might smell of roasted or fermented foodstuff, whereas aromatic alcohols (phenols) are components of smoked food.

Most of the examples in Table 1 are chosen from different types of food to make the odours easier to demonstrate. You could randomly distribute appropriate plant and food samples on a large surface, and ask students to group the exhibits according to their smell (you could help by providing the attributes ‘floral’, ‘rancid’, ‘fruit’, ‘vegetable’, ‘spicy’ and ‘smoke’). When the students are done, let them compare their results with the chemical classification given in Table 1.
Bearing the structural characteristics in mind, the next question is how we use smell to distinguish between these differences in functional groups, sizes and overall shapes of molecules. In many physiological processes taking place at cell membranes, a receptor is activated after a ligand binds to its extracellular domain. This principle is often depicted as a key fitting into a lock – only the right key opens the corresponding lock – as the docking ligand has high specificity for its acceptor site on the receptor.

Table 1: Classification of volatile organic compounds according to their functional groups and characteristic odours

Odorant receptors

Some of the most fascinating features of the physiology of smell were discovered by the 2004 Nobel Prize winners Linda Buck and Richard Axel. In contrast to the simple but specific key-lock model that governs taste, smell is dictated by a whole set of sensory cells. One type of fragrant molecule interacts with more than one receptor type, so the overall sensation is created by the combination of activated receptors. When they tested a series of aliphatic n-alcohols on individual mouse neurons, Buck and co-workers found that clusters of olfactory neurons were activated. For example, pentanol weakly stimulated a receptor called S3; hexanol strongly activated S3 and S25; heptanol S3, S19 and S25; octanol S18, S19, S41 and S51; and nonanol S18, S19, S41, S51 and S83. Thus, a single odorant is recognised specifically by multiple odorant receptors working in combination.

Such a pattern of receptor activation creates a vast repertoire of perceivable odours. Indeed, it is estimated that we can remember about one thousand odours and distinguish between an order of magnitude more, depending on our age, experience and natural sensitivity. Our linguistic ability to name scents, however, lags far behind our nose’s ability to discern them. The food industry trains experts to recognise subtle nuances of smells. For example, diluted essential oils or isolated compounds representing a certain aroma are applied onto a strip of odourless filter paper and placed into a screw-top glass vial (see below).

You could offer your students oregano (1% carvacrol in propylene glycol), rose (1% essential oil in ethanol), lemon (10% essential oil in ethanol), cinnamon (5% cinnamaldehyde in propylene glycol), a fruit aroma (5% in propylene glycol) or bitter almonds (1% benzaldehyde in propylene glycol) in such an experiment. Either the student must choose from a list of about 20 odorants or he or she is asked to describe and name the scents without the help of given attributes (see Experiment 1 in the classroom activityw1).

Sample presentation for a smell test. Glass vials contain filter paper strips that are soaked in diluted essential oil Image courtesy of Angelika Börsch-Haubold

Students identifying scents Image courtesy of Angelika Börsch-Haubold

An untrained person may correctly associate an odorant with its source or something that contains it, but still fail to identify the original substance. In a course on the sensory evaluation of food that I recently taught, only half of the students recognised the aroma of oregano; a quarter of them confused it with thyme or marjoram, which are closely related herbs; and others identified the scent as rosemary, basil and parsley, which are less closely related herbs with quite distinct flavours. However, some students correctly associated the odour with tomato soup, which may be flavoured with oregano. Two-thirds of the class recognised the smell of roses, some students associated it correctly with similar flowers such as lilac or melissa or with perfume, but others incorrectly suggested mint, medicine and spice.

Almost all students recognised bitter almonds, mint and cinnamon, but failed to identify sage and coriander. When the solutions were revealed, everybody immediately recognised the smells that had previously eluded them, demonstrating that olfactory memory is far better than our ability to actually name a particular smell.

Small changes in the chemical structure – distinct smells

The fine-tuning of our receptor machinery allows us to distinguish between chemically similar molecules. Many fragrances are derived from plants, and plant products can be used to demonstrate how small changes in the chemical structure of an odorant give rise to either completely different smells or at least distinguishable flavours (see illustrated structures). The examples are sorted by the following chemical principles:

1. Elongation of a carbon chain: adding two methyl groups (‑CH₂‑CH₂‑) to the odorant of coconut, g-nonalactone, gives the odorant of peach; inserting a vinyl moiety (‑CH=CH‑) into benzaldehyde (bitter almonds) yields cinnamaldehyde (cinnamon).
2. Exchange of a functional group: replacing the aldehyde group of the vanillin molecule with an allyl group (‑CH₂‑CH=CH₂) gives eugenol, the fragrance of cloves. The alcohol 1-butanol smells pungent whereas the corresponding carboxylic acid (butyric acid) smells like rancid butter or vomit.
3. Addition of a functional group: adding a methoxyl group to benzaldehyde changes its smell from bitter almonds to aniseed.
4. Position of the functional group: carvacrol, which has an ‑OH group next to a ‑CH₃ group, smells like oregano, whereas thymol, which has an ‑OH group next to a ‑CH(CH₃)₂ group, smells like thyme; 1-propanol smells ethanol-like, whereas 2-propanol smells sweet (the numbers reflect the position of the -OH group).
5. Exchange of aliphatic and aromatic rings: replacing the benzene ring of thymol with cyclohexane produces menthol which smells completely different.
6. Stereochemical differences: usually, one enantiomer of a chiral flavour molecule elicits a strong odour whereas the other is weak. Notable exceptions are (S)-(+)-carvone (the aromatic ingredient of caraway seeds) and (R)-(–)-carvone (spearmint). (S)-(–)-limonene smells like turpentine (pine) but (R)-(+)-limonene has the odour of oranges.

Chemically similar compounds smell different Images courtesy of Angelike Börsch-Haubold

However, there are compounds that are structurally unrelated but smell similar. Cyclooctane, camphor and 1,8-cineol all have a camphoric odour, although cyclooctane consists of an all-carbon single ring structure (C₈H₁₆) whereas camphor and 1,8-cineol are both bicyclic molecules with a functional group containing oxygen. The so-called ‘green note’ of unripe fruit and vegetables, which is added to cosmetics for a scent of ‘freshness’, comes from a group of closely related C₆ aldehyde compounds (cis-3-hexenal: fresh tomatoes; cis-2-hexenal: green apples; trans-2-hexenal: green and black tea, fresh tomatoes). Similarly, the alcohol cis-3-hexenol (freshly cut grass), the C₉ aldehyde 2-trans-6-cis-nonadienal (cucumber peel), an aldehyde attached to a ring structure (the grassy-smelling ligustral) and even some pyrazines (2-propyl-3-methoxypyrazine: bell peppers) have this ‘green note’.

Plants are nature’s perfume factory

By using the wide range of odorants contained in plants, you can combine organic chemistry with the physiology of smell to demonstrate how well we understand our environment without being fully aware of it. If you want to focus on training the sense of smell, you could ask your students to sort different dilutions of one odorant by increasing intensity (see Experiment 2 in the classroom activityw2). These two activitiesw1, w2 should stimulate students to link everyday situations with chemistry and make them curious about the description of our world in terms of chemical compounds.

Lavender Image courtesy of Angelika Börsch-Haubold

Acknowledgements

I would like to thank the students from the sensory training course (Fachhochschule Weihenstephan, Winter semester 2006/07) for the preparation of odorant samples and for stimulating discussion.

Web references

w1 – Experiment 1: Test your sense of smell. The experimental protocol, including the necessary worksheets, can be downloaded here

w2 – Experiment 2: Sort a dilution series of an essential oil. The experimental protocol, including the necessary worksheets, can be downloaded here

Resources

Buck LB (2004) Unraveling the Sense of Smell. Nobel Lecture, 8 Dec, Stockholm, Sweden.

Busch-Stockfisch M (ed; 2005) Praxishandbuch Sensorik in der Produktentwicklung und Qualitätssicherung. Hamburg, Germany: Behr’s Verlag

Malnic B, Godfrey PA, Buck LB (2004) The human olfactory receptor gene family. Proceedings of the National Academy of Sciences USA 101: 2584-2589

Malnic B, Hirono J, Sato T, Buck LB (1999) Combinatorial receptor codes for odors. Cell 96: 713-723

Steinegger E, Hänsel R (1988) Lehrbuch der Pharmakognosie und Phytopharmazie. 4th Ed. Berlin, Germany: Springer-Verlag

Dr Angelika Börsch-Haubold, who is a trained pharmacist and pharmacologist, teaches regularly at the Fachhochschule Weihenstephan in Freising, Germany.