Compound Interest: The Chemistry of Watermelons: Colour, Aroma, & Explosions (2024)

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Compound Interest: The Chemistry of Watermelons: Colour, Aroma, & Explosions (1)

Watermelons are a popular, refreshing summer fruit. There’s also a lot of intriguing chemistry behind them, from the colour of their flesh and the complexity of their aroma to the tales of explodingwatermelons in China, and even the claims that they can have a Viagra-like effect. This post takes a look at each of theseand the molecules behind them.

Let’s start with the colour. Everyone’s familiar with the vivid pink colouration of watermelon flesh. Of course, there are some varieties of watermelon that don’t actually exhibit this colouration, but it’s the pink-fleshed watermelon that’s by far the most popular. The cause of this colouration is a chemical called lycopene.

Lycopene is a carotenoid pigment, like beta-carotene (the compound that gives carrots their orange colour). It’s also found in tomatoes, and responsible for their red colour. Watermelon actually contains even higher levels of lycopene than tomatoes; it can contain up to an estimated 72 micrograms per gram, whilst the raw tomato maximum is estimated at 42 micrograms per gram. Lycopene has been linked with a range of health benefits, though the scientific evidence for the majority of these is currently conflicted or limited.

Watermelon aroma, on the other hand, has been extensively researched. This is perhaps partly a result of watermelon flavour being notoriously hard to produce artificially, and a number of studies have tried to pin down the exact molecules that contribute to its aroma and taste. The aroma molecules are produced as a consequence of the watermelon being cut into – this releases enzymes from cells in the melon, which in turn aid the oxidation of fatty acids into aroma compounds.

The view on the main components of watermelon aroma has differed over the years. Initial studies suggested that the primary odourants were C6 and C9 alcohols. (Z,Z)-3,6-nonadien-1-ol, in particular, was suggested as the predominant compound contributing to the aroma, and has a smell individually described as ‘watermelon rind-like’. The alcohols were suspected due to their relatively high concentrations; however, they also have higher odour threshold values (the level at which they can be detected by the human nose) than some of the other compounds in the aroma mixture.

It’s now thought that it’s the C6 and C9 aldehydes that make the main contribution to the watermelon aroma. It was suggested that previous researchers had failed to realise this, as they collected the compounds over long periods of time, during which enzymatic action converted the aldehydes into alcohols. Scientists now think that (Z,Z)-3,6-nonadienal is the predominant watermelon odourant and that several other aldehydes also contribute. One of these is (Z)-3-hexenal, the same compound largely responsible for the smell of fresh-cut grass – helping to explain why many people may find the two aromas similar.

Whilst (Z,Z)-3,6-nonadienal may well be the compound that gives watermelon much of its distinctive aroma and flavour, it’s unfortunately easily broken down, which limits its potential for use as an artificial flavouring. Attempts to produce structurally similar esters that might provide a similar aroma and flavour have also been unsuccessful to date, so it doesn’t look like the problem of substandard watermelon flavourings is one that’s going to go awayany time soon.

Watermelon chemistry has made the news for a number of reasons. One of these is its supposed Viagra-like effect, with some websites even referring to it as ‘nature’s Viagra’. The chemical reasoning was that watermelons contain decent levels of citrulline, which is metabolised into arginine in the body. Arginine is an amino acid involved in the synthesis of nitric oxide in the body, which in turn is associated with the widening of blood vessels. It does this by increasing levels of cyclic guanosine monophosphate (cGMP).

Now, Viagra works by breaking down an enzyme (phosphodiesterase type 5) responsible for breaking down cGMP. Watermelon doesn’t have any effect on this enzyme, so proclaiming it as a natural alternative to Viagra is inaccurate. Additionally, even if watermelon did have an organ-specific effect, you’d have to eat a lot of watermelon to significantly boost your levels of arginine, and there’s no evidence that arginine by itself would boost anyone’s ability to gain an erection anyway.

Another more amusing watermelon chemistry story hit the news back in 2011. Farmers in Eastern China were confronted by the comical-sounding sight of acres of watermelons spontaneously exploding over a period of a few days. As it turned out, it was most likely due to the misuse of a growth-promoting chemical, forchlorfenuron.

Forchlorfenuron is approved for use on kiwi fruits, grapes and raisins in the US, and whilst its use is completely safe, it’s not considered appropriate for use on watermelons. The reason for this is that it leads to somewhat misshapen fruit, and also causes the seeds to turn white. It’s thought the Chinese farmers used too much of the growth chemical on their watermelons, and at the wrong time of the year, during a particularly wet period. They also used it on a particularly thin-rinded melon, so all of these factors made the ultimate fate of their crop grimly predictable.

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References & Further Reading

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  • Compound Interest: The Chemistry of Watermelons: Colour, Aroma, & Explosions (2)

    misterken

    Posted June 9, 2015 at 8:18 pm 0Likes

    so maybe the presence of nonadienal compounds is the reason why cucumbers and watermelon have a similar odor profile (at least to me).

    • Compound Interest: The Chemistry of Watermelons: Colour, Aroma, & Explosions (3)

      Compound Interest

      Posted June 9, 2015 at 8:58 pm 0Likes

      Absolutely – in fact the ‘cucumber aldehyde’, trans,cis-2,6-nonadienal, is present in both cucumbers and watermelon.

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  • Compound Interest: The Chemistry of Watermelons: Colour, Aroma, & Explosions (4)

    Sal2388

    Posted October 26, 2016 at 4:03 am 0Likes

    Speaking of the cucumber aldehyde, trans,cis-2,6-nonadienal. Do you know if this is present in pheasant back mushrooms, also known as polyporus squamosus? I like to forage mushrooms specifically morels, and have found these often. They give off a watermelon rind or cucumber aroma.

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Compound Interest: The Chemistry of Watermelons: Colour, Aroma, & Explosions (2024)

FAQs

What are the aroma compounds in watermelon? ›

The flavor compounds in watermelon juice are mainly C6 and C9 aldehydes, ketones, and alcohols, such as nonanal, (E)-6-nonenol, (Z,Z)-2,6-nonadienal, (Z)-3-nonenal, (E,Z)-2,6-nonadienal, and (Z,Z)-3,6-nonadienal [7,8]. Development of off-flavor is an unavoidable issue in the thermal processing of watermelon juice; ...

What is the chemical smell of watermelon? ›

“Whilst (Z,Z)-3,6-nonadienal may well be the compound that gives watermelon much of its distinctive aroma and flavour, it's unfortunately easily broken down, which limits its potential for use as an artificial flavouring.

What chemical compounds are in watermelon? ›

Lycopene was first reported in watermelon in 1930 (30), and like tomato, watermelon contains high levels of lycopene and other carotenoids with potential benefit for human health (31, 32). The health benefits of some of these compounds are known and continue to be the focus of nutrition research.

What are the chemical properties of watermelon? ›

The watermelon plant contains five unsaturated fatty acids called 9-hexadecenoic acid, 9-octadecenoic acid, 9,12-octadecadienoic acid (Z,Z), 8, 11-octadecadienoic acid and 9,12,15-octadecatrienoic acid at 9.96, 10.8411. 78, 13.02 and 13.21 min retention times, respectively [Table 2].

What chemical makes watermelon red? ›

Lycopene is the source of the red color in several fruits, notably watermelon (Citrullus lanatus var. lanatus) and tomato (Solanum lycopersicum). The pigment, also known as ψ,ψ-carotene, is a linear polyolefin that contains eight isoprene units.

What are the volatile compounds in watermelon? ›

The dominant volatiles (at least 2% peak area in all samples) being known watermelon flavor compounds including hexanal (12.7–15.1%), (E)-2-nonenal (7.4–13.0%), (Z)-3-nonen-1-ol (8.1–12.3%), 6-methyl-5-hepten- 2-one (6.4–8.4%), (E,Z)-2,6-nonadienal (5.3–9.8%), (Z)-6-nonenal (2.1–6.6%), nonanal (4.4– 6.0%), (Z,Z)-3,6- ...

What compound has a fruit like smell? ›

Esters have a fruity smell due to their volatile nature caused by their chemical composition and conformations.

Which chemical compound has fruity smell? ›

Ester. Explanation: The fruity smell is of an ester.

What does watermelon scent do? ›

AOPING Watermelon essential oil has a sweet, soft, soothing fruity aroma. It is not as enthusiastic as tropical fruits, and its gentle scent slowly calms the heart, bringing a fresh and peaceful atmosphere.

What is watermelon concept in chemistry? ›

Thomson's atomic model was also called the plum pudding model or the watermelon model. The embedded electrons resembled the seed of a watermelon while the watermelon's red mass represented the positive charge distribution.

What is watermelon model in chemistry? ›

J. J. Thomson proposed the watermelon model of the atom which is also known as the plum pudding model in which electrons are present inside the atom-like plumb in the pudding.

What was the original color of the watermelon? ›

First grown in Africa about 5,000 years ago, yellow watermelons went through generations of selective cross-breeding for texture, color and sweetness before any pink variety ever appeared. As the lycopene content of hybrid varieties increased over time, the fruit naturally became redder and redder.

What enzyme is in watermelon? ›

Some enzymes, including OSC, cytochrome P450 (CYP), acetyltransferase (ACT), and UDP-glucosyltransferase (UGT), which are potentially involved in the biosynthesis of cucurbitacins, have been isolated and characterized from pumpkins (Cucurbita pepo), watermelons (Citrullus lanatus), cucumbers (Cucumis sativus), and ...

What bioactive compounds are in watermelon? ›

Watermelon provides a wide variety of dietary antioxidants such as carotenoids (lycopene and β-carotene), phenols, vitamins (A, B, C and E) and specific amino acids (citrulline and arginine) (Perkins-Veazie, 2002, Perkins-Veazie et al., 2007), which are thought to exert a protective role in reducing the risk of certain ...

What are the chemicals in fruit aroma? ›

Fruits produce a range of volatile compounds that make up their characteristic aromas and contribute to their flavor. Fruit volatile compounds are mainly comprised of esters, alcohols, aldehydes, ketones, lactones, terpenoids and apocarotenoids.

What compounds are in watermelon rind? ›

The composition of watermelon rind mostly consists of celluloses, hemicelluloses, pectins, and lignins, along with entrapped sugars, lycopene, carotenoids, citrulline, and phenolics [11] . The watermelon rind extract demonstrates antioxidant and antibacterial properties because of the presence of polyphenols. ...

What gives watermelon its flavour? ›

Today, it is believed (Z,Z)-3,6-nonadienal is considered to be the main contributor of watermelon flavour. However other watermelon aldehydes also contribute to this flavour too. For example, the 'leaf aldehyde' cis-3-Hexenal is also found in watermelon and has an intense grassy-green odour.

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