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  • Humans love to make perfumes and fragrances from the weirdest sources,

  • from endangered plants, to extremely expensive marine poop,

  • to the crotch glands of rare animals.

  • And historically, people have gotten so excited over these strange

  • sources of scent that we've exploited them to near extinction.

  • So, chemists trying to protect the environment had to come up

  • with synthetic ways to reproduce natural fragrance compounds.

  • Now, that's harder than you might think.

  • Because we can't just 3D print any molecule we likeat least, not yet.

  • It's a complex puzzle requiring just the right ingredients,

  • and it's different for every chemical.

  • And often, the synthetic solution to one sustainability disaster

  • creates new trouble of its own,

  • from health problems to environmental contamination.

  • So here are four stories of how humans exploited a source of natural fragrance,

  • then tried to save it through synthetics

  • and then had to save themselves from the chemicals that they made.

  • If you take a whiff of perfumes like Light Blue by Dolce & Gabbana

  • or Midnight Poison by Christian Dior, you might detect a subtle musky aroma.

  • Some have likened it to the wood in old churches.

  • But it comes from ambergris.

  • In addition to smelling nice, it fixes perfume on the skin so the scent lasts longer.

  • Ambergris looks like a yellow-gray rock that washes up on beaches.

  • And for millennia, people used it for medicine, incense, and perfume

  • without knowing what it was.

  • Perfumers theorized it might be anything from petrified lynx urine

  • to a kind of amber.

  • Hence the French name, “ambergris,” meaning gray amber.

  • But we eventually figured out its true nature.

  • It's sperm whale poop!

  • A sperm whale eats around 400 kilograms of squid per day.

  • But it can't digest their beaks.

  • Researchers think the whale produces compounds

  • in its gut to help protect itself from those hard, poky beaks.

  • And we think those anti-beak compounds are what go into making ambergris.

  • Once expelled, this block of feces floats through the ocean,

  • where it can eventually wash up on a beach and work on its tan.

  • But finding this highly prized poop is a pretty rare occurrence.

  • Only 1% of sperm whales make ambergris.

  • And only about 0.5% of the substance's mass converts into odor compounds.

  • So ambergris is pricey.

  • Plus, sperm whales are in danger of extinction.

  • Meaning in some countries, ambergris isn't just expensive,

  • it's flat out illegal to buy and sell.

  • But it's still really useful for perfume.

  • So scientists have scrambled to make a synthetic equivalent.

  • But first, they had to analyze its chemistry.

  • Up to 45% of ambergris is ambrein,

  • an odorless organic compound that scientists think

  • is created by the whale's gut bacteria.

  • Ambergris also contains light-sensitive substances called porphyrins.

  • When porphyrins absorb light,

  • the energy from that reaction creates super-unstable oxygen compounds

  • that transform ambrein into aromatic compounds including ambrox.

  • And in the 1940s, ambrox was identified

  • As the main fragrance compound in ambergris.

  • In 1950, a Swiss company identified ambrox's chemical structure

  • and developed a way to synthesize it from a plant: clary sage.

  • But even though it helps preserve sperm whales,

  • the industrial synthesis of ambrox is very resource-heavy.

  • It also uses large amounts of toxic substances, like chromium trioxide,

  • which can induce genetic defects and is highly dangerous to aquatic life.

  • So even though scientists had a way to make fake ambergris,

  • they needed to do better.

  • Researchers discovered that, by changing out certain chemicals,

  • for example by using hydrogen peroxide,

  • they cut down on the chemical waste generated in the process.

  • And those tweaks also meant they got 20 times more stuff out of the process.

  • Which is great news for fans of sperm whale poop across the world.

  • Now, another musky-scented animal discharge is, musk.

  • This earthy, animalistic odor has been used in perfumes for thousands of years.

  • It's also been used as an aphrodisiac,

  • on the basis that some animals use it to attract mates.

  • See, undiluted musk is a pee-smelling secretion

  • from the scent glands of some mammals.

  • There are other animals that make musk.

  • But in the perfume industry, “muskusually refers specifically to

  • secretions from a gland near the genitals of the male musk deer.

  • And because musk was so desirable, people hunted the deer nearly to extinction.

  • Clearly, chemists needed to invent an alternative.

  • But as it turned out, the first synthetic musk was produced by accident.

  • In 1888, a researcher trying to create better explosives

  • accidentally made something that smelled like musk.

  • Soon after, the synthetic nitro musk craze exploded.

  • And nitro musks have formed a big part of most perfumes,

  • including the famous Chanel N°5.

  • But in 1981, Japanese scientists were the first to

  • sound the alarm about how dangerous nitro musks might be.

  • Synthetic musks accumulate everywhere, both in the environment,

  • and in the bodies of animals.

  • They've been found in rivers, lakes, fish, birds and mammals,

  • including human blood and breastmilk.

  • Now, we don't know for sure that they're toxic to humans.

  • But animal studies show that nitro musks can

  • inhibit the activity of proteins that allow cells to expel toxins.

  • And since that can cause cancer,

  • the use of nitro musks in cosmetic products has been banned in many countries.

  • The perfume industry has largely replaced them with polycyclic musks,

  • which account for 90% of all musky scents used in the perfume industry.

  • But it turns out that was a bit of an oopsie,

  • because polycyclic musks have been found to accumulate in environments

  • and organisms basically as much as their nitro cousins.

  • And early research suggests they can be toxic to marine life.

  • So it turns out that's not the alternative we were looking for.

  • But one does exist.

  • And it involves something that doesn't just smell like musk.

  • It's actually part of musk.

  • Back in 1906, scientists isolated the

  • main aromatic compound in deer musk and called it muscone.

  • Chemists started synthesizing muscone in 1934.

  • And it seems like it's not too hard, for example,

  • it's possible to use citronella oil as a starting point.

  • Muscone is a type of macrocyclic musk,

  • which are much more expensive and complicated to synthesize

  • than their polycyclic cousins.

  • But in theory, they should have less environmental impact because

  • they break down more easily, so they shouldn't accumulate so much.

  • Plus, their price is expected to come down as our technology improves

  • and we get better at making them.

  • Now, not every fragrant compound involves animal excretions.

  • Sometimes, we derive scents from plants.

  • And one of the most legendary is sandalwood.

  • Species of sandalwood tree grow naturally everywhere from Fiji to Chile.

  • But in perfumery, the wordsandalwood

  • usually refers to Santalum album, a species native to India.

  • Their woody, spicy fragrance comes from the wood and its oil.

  • And it's been used in medicine, religion, and perfumery since Ancient Egypt.

  • These days, sandalwood scent is used in incense, lotions,

  • and perfumes like Dior's Hypnotic Poison or Crystal Noir by Versace.

  • Starting in the 18th century, the Indian government held a monopoly

  • on sandalwood trade, and commercial planting was forbidden.

  • Sandalwood trees became really hard to come by,

  • driving the price so high that sandalwood oil is sometimes calledliquid gold.”

  • In addition, sandalwood suffered decades of devastating fires,

  • disease and smuggling.

  • In the 90s, it was designated as in danger of extinction in the wild.

  • The Indian government has since relaxed its planting restrictions,

  • and plantations have been popping up in countries like Australia and Indonesia.

  • But, it can take 15 years until sandalwood is ready to harvest.

  • So it will be a while before the new plantations can top off the shortage.

  • Meanwhile, most of the perfume industry chooses the synthetic option.

  • Researchers identified the structure of santalol,

  • the main aromatic compound in sandalwood, in 1921.

  • But it wasn't until 1991 that scientists discovered that

  • the true essence of sandalwood lies in only one isomer of santalol.

  • An isomer is a version of a compound that has the same number

  • of the same atoms, but they're arranged differently.

  • With this discovery, chemists were able to

  • more accurately synthesize the scent of sandalwood.

  • But they still had to deal with the environmental impacts of the process.

  • Santalol is synthetized from pine resin,

  • which can be extracted without killing the tree.

  • But the synthesis generates a lot of chemical waste

  • that needs to be treated and stored.

  • And it can also contaminate soil and water.

  • So researchers are working on new catalysts that would

  • limit the environmental impact of synthetic sandalwood production

  • until the trees can bounce back.

  • Another aromatic plant that's a victim of its own popularity is vanilla.

  • It's a type of orchid native to Mexico,

  • and it was highly valued by the ancient Aztecs,

  • who used it to flavor their chocolate drinks.

  • Today, it's mainly grown in Madagascar and Indonesia.

  • And because it's been exploited and its habitat has been destroyed,

  • vanilla is a protected species in the wild.

  • But even in industrial conditions, cultivating it is a difficult process.

  • See, when colonizers took vanilla plants from Mexico to other countries,

  • they didn't take their pollinators along for the ride.

  • So, vanilla flowers need to be pollinated manually, one by one.

  • And it takes 600 pollinated flowers to make a kilogram of vanilla beans.

  • And the beans only contain 2% of the main flavor compound, vanillin.

  • Part of the world's demand for vanilla is still satisfied

  • by extracts distilled from the beans,

  • because consumers prefer to see the labelnaturalon vanilla-flavored products.

  • But this growing desire forall naturalingredients jacks up the price of vanilla,

  • which has risen by 2,000% since 2012 and comes close to the price of silver.

  • That's why around 90% of the world's vanilla flavor comes from synthetic vanillin.

  • Vanillin was first synthesized in 1874 from coniferyl alcohol,

  • which is obtained from pine bark.

  • In 1876, the industry switched to a more efficient method

  • using compounds derived from petroleum and clove oil.

  • In the 1930s, the dominant process switched again to one that

  • used natural ingredients that people assumed were more sustainable:

  • the waste from paper production.

  • This method uses lignin, the main ingredient of wood.

  • Lignin naturally degrades to vanillin,

  • giving second-hand bookstores that classic sweet smell.

  • Most vanillin came from lignin until the early 1990s,

  • when a change in how paper is produced

  • made that cheap waste product less available.

  • People also started looking at the whole lifecycle of a product.

  • And they noticed that, even though reusing industrial waste sounded sustainable,

  • making vanillin from lignin generates 160 tons

  • of highly corrosive waste per one ton of vanillin.

  • These days, more than 90% of vanillin is synthesized from petroleum.

  • The process generates little waste compared to the earlier methods.

  • Vanillin is used in around 2% of all food products,

  • in multiple perfumes and colognes,

  • and in the pharmaceutical synthesis of drugs like levodopa,

  • one of the main treatments for Parkinson's disease.

  • So because vanillin is everywhere,

  • even tiny steps toward making its synthesis greener

  • go a long way towards preserving the environment.

  • But we can definitely still do better.

  • Because as we mentioned, vanillin comes from petroleum,

  • which ties it to the oil trade.

  • So researchers have been looking for more sustainable alternatives.

  • One new approach makes vanillin from ferulic acid, which is found in many plants.

  • By the way, another natural source of vanilla-like scent

  • does come from animal excretions.

  • In this case, glands on a beaver's butt.

  • So, synthetic versions of natural fragrances have a lot of advantages.

  • They can protect vulnerable species, and they generally don't involve animal butts.

  • Also, manufacturers can be sure they don't contain unwanted allergens,

  • which can happen with natural fragrances.

  • But let's be honest.

  • A lot of companies that turn to synthetics are trying to save money.

  • Not exploiting a natural resource is more of a side effect.

  • So that does nothing to ensure synthetic alternatives

  • will be good for the environment.

  • It's a good reminder that we can't really tell how good or bad a chemical is

  • for the environment without looking at the whole picture,

  • how it's made and where that stuff comes from.

  • And it's a reminder that even when we fix something that we were doing wrong,

  • we can often still do better.

  • And smell great while we're at it.

  • Thank you for watching this episode of SciShow,

  • and thanks to this month's President of Science, Matthew Brant,

  • for helping us make it happen.

  • Your support means a lot to us.

  • And so do all of our patrons, so thanks to you too!

  • If you want to get involved and help us make SciShow,

  • you can head over to patreon.com/scishow.

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