Gardenia

The weather warms, so my gardenia buds open, seeking attention and permeating the night air with their perfume. As I made a study of the fragrance, I decided to write on this nature’s wonder. The common gardenia (Gardenia jasminoides) has highly fragrant white flowers. In the evening, the opening buds smell slightly green and piquant because of the salicylate aspect. The flowers also smell creamy, recalling coconut and peach skin. There is an unmistakably heady indolic element of jasmine. In ripe blooms, they have a sharp green ‘mushroom’ overtones. Gardenias also share some aspects with lily, lily of the valley, ylang ylang, and a bit of rose.

In terms of composition, (E)-ocimene, linalool, methyl benzoate and a number of tiglates compose the gardenia flower headspace. However, there are likely olfactory variations amongst species. For example, the critically endangered native of Hawaii Gardenia brighamii, as demonstrated by headspace analysis of its gas-phase components, contains 41% methyl benzoate, 13% (3Z)-hex-3-enyl benzoate, 7% indole that recalls ‘white-flower smell’, 7% jasmine lactone that lends the jasminic and coconut touch, and 3.7% (3Z)-hex-3-enyl tiglate that gives the tang of soil fungi and mushrooms to the flower. It is possible to extract the desired fragrance from their flowers by enfleurage as the villagers of Fusagasugà in Colombia have continued to produce gardenia absolute since 1945. However, such enfleurage-derived absolutes are rarely ever produced in industrial scale due to the exorbitant costs involved. And, yet, I have stumbled upon a solvent-extracted absolute of the Tahitian gardenia or Tiaré (Gardenia tahitensis) which can be used in fine fragrances up to 1% of a composition to impart the exotic white-floral quality.

Gardenia in Perfumery

Like many flowers that do not yield the desired quality of their scents or do so at a prohibitive cost of extraction, the smell of gardenia is also the object of fascination in perfumery. Early reconstitutions of gardenia often revolve around a tuberose note and aldehyde C-18 and may eschew styrallyl acetate altogether. Still, most gardenia bases almost always call for it. Such bases rely on its powerful rhubarb-like green note in combination with jasmine, rose, lily of the valley, lilac, and a small amount of orange blossom to render gardenia odour characteristics. But styrallyl acetate is rather harsh, so salicylates may be used to soften it along with aldehyde C-14 and C-18 as modifiers. The top note of such bases may call for aldehyde C-8 to C-12 and citrus oils such as lemon, mandarin, orange, or bergamot. To fix the components, heliotropin, coumarin, musk, labdanum, myrrh, tolu balsam, cinnamic alcohol, and synthetic ambergris may be used.  Other aroma chemicals such as the mildly floral ‘gardenia oxide’ (isoamyl benzyl ether) and the citrusy fruity linalyl isovalearate are sometimes incorporated into gardenia compounds. Meanwhile, perfumer Jean-Claude Ellena, who professes his love of simplicity, draws a more-or-less complete gardenia note with just three ingredients: the fruity sweetness and coconut of aldehyde C-18 (γ-nonalactone), the fresh green of styrallyl acetate (Gardenol), and the Concord-grape sweetness of methyl anthranilate. Indeed, the reconstitution of gardenia is subject to the creative interpretation of the perfumer.

Gardenia in Perfumes

In fine fragrances, gardenia was initially a secondary floral. It formed part of the composition, but was itself not featured. For instance, gardenia found its way into the floral aldehydic L’Aimant (Coty, 1927) via the styrallyl acetate contained in infusions of jasmine, cassie, and tuberose used in the original formula. The green freshness of gardenia pairs well with chypre accords in perfumes such as Bandit (Robert Piguet, 1944), Ma Griffe (Carven, 1947), Miss Dior (1947), Cabochard (Grès, 1959), Coriandre (Jean Couturier, 1973), Michelle (Balenciaga, 1979), and the excellent fruity chypre La Panthère (Cartier, 2014).

Gardenia as main floral theme can be seen starting from soliflores like Gardénia (Chanel, 1925) and Jungle Gardenia (Tuvaché, 1933). If you like your gardenia creamy, Lou Lou (Cacharel, 1987) offers an interesting interpretation of the creamy Tahitian gardenia or Tiaré based on an oriental accord and tuberose. Another very creamy, coconut-like gardenia is Crystal Noir (Versace, 2004). But if you like the company of magnolia and jasmine, the bright gardenia of Un Matin d’Orage (Annick Goutal, 2009) may suit you better. A recent resurgence of the note seems to have produced a slew of gardenias for everyone, ranging from the sombre gardenia of Une Voix Noire (Serge Lutens, 2012), the fruity frangipani and gardenia of Gorgeous Gardenia (Gucci, Flora, 2012), to a full-fledged gardenia offered in the masculine context of Boutonnière No.7 (Arquiste, 2012). But for those who crave a more realistic impression, Gardénia (Robert Piguet, 2014) offers a no-frills flower with minimal contrasts.

mom gardenia

As for me, I cannot quite pick a favourite gardenia perfume at the moment. My pot of gardenia has had all the attention from me — perhaps, the only other rivals are the gardenias in my mother’s garden.

Sources: enfleurage.com, firmenich.com, P&F Vol.8 October/November 1983 by Danute Pajaujis Anonis, Perfumery: Practice and Principles; Scent and Chemistry The Molecular World of Odors, Scents of the Vanishing Flora

  1. Müller PM, Lamparsky D. Perfumes: Art, Science & Technology. Amsterdam, New York: Elsevier, 1991
  2. Tamogami S et al. Analysis of enantiomeric ratios of aroma components in several flowers using a Chiramix column. Flavour Fragr J 2004;19:1-5.
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Mapping The Classic Chypres

Whilst making a study of the classic chypres, I realised that they borrowed from one another in more ways than I could have perceived from sniffing alone. However, the results were anything but copies. By determination and strokes of ingenuity, their creators produced very original and creative compositions. In order to see the big picture of how each composition was inspired or influenced by the others, I drew the diagram of these timeless compositions whose traditional chypre structure dotted the landscape of perfumery.

chypre map.jpg

Chypre de Coty ( Coty, 1917) consolidated the structure of chypre family. Two years later, Jacques Guerlain appropriated the structure for the ripe peach skin and Guerlinade of Mitsouko (Guerlain, 1919). This ripe peach was later put at the fore by Edmond Roudnitska in Femme (Rochas, 1942).

Inspired by Chypre de Coty, Jean Carles used the classical structural materials in Ma Griffe (Carven, 1946) and built the composition with bases, which are bold accords based on synthetic and natural ingredients. This gave Ma Griffe a strong structure and an exceedingly complex quality. He would later apply this technique to Miss Dior (1947) with a  nod to the galbanum of Vent Vert (Pierre Balmain, 1945) by Germaine Cellier. Even though I do not see Vent Vert as a chypre, I put it there because Miss Dior was indubitably influenced by it.

And, although its inspiration involves the leather accord based on isobutyl quinoline, Bandit (Robert Piguet, 1944), also by Germaine Cellier, still clearly screams of chypre. This brutal combination of leather and chypre was reworked by Bernard Chant in Cabochard (Grès, 1959) to make it more accessible with a floral emphasis and softer character. He would go on to establish this leather chypre accord in masculine perfumes with Aramis (1965) that retains some of the softness of Cabochard, but darkens its leather. I almost forgot to include another noteworthy creation, but thanks to Robert who mentioned  Azurée (Estée Lauder, 1969). Possibly by Bernard Chant as well, it  bears striking similarity to Aramis and Cabochard. And, of course, Bernard Chant was creative with Aromatics Elixir (Clinique, 1971), dosing the patchouli and floral notes whilst reducing the animalic touch to simply the castoreum puffs. Aromatics Elixir, thus, sets itself uniquely between a chypre and an oriental.

Charles Hard Townes, in his Nobel prize speech, commented, ‘Scientists do, as we have heard, stand on the shoulders of giants from the past’ — I could not agree more.

Review: Grès Cabochard — 5.0 points

Inspired by the ferocious whip of Bandit (Robert Piguet, 1944), perfumer Bernard Chant took to the leathery character and created Cabochard (Grès, 1959). The leather accord was softened and balanced with verdancy and florals. Cabochard itself would become a legacy amongst the family of leather chypres and inspire a number of perfumery’s classics such as Aramis (1965) and Chanel N°19 (1970).

fragrantica

From the start, the green combination of galbanum, armoise, and basil contrasts nicely with the earthy character. Styrallyl acetate in combination with aldehyde C-11 (undecylenic aldehyde) contribute to the green floral aspect. To complement the green, there is the freshness of mandarin and bergamot with linalool and linalyl acetate. The opening is certainly reminiscent of another era: bitter green with sharp freshness. It is bright and sparkling.

The composition reveals the floral heart as expected of a classical chypre. It is dominated by a bright jasmine accord different from those of Ma Griffe (Carven, 1946) or Miss Dior (1947), a fresh rose note, and hyacinth. Its radiance is imparted by a muguet note. Also, the relatively high content of sandalwood compared to other chypres provides the apparent softness to Cabochard. Such pairing of the jasmine accord and sandalwood would later be found in the masculine leather chypre territory of Aramis.

Then, glimpses of leather appear. Along with isobutyl quinoline, balsamic benzoin, a castoreum note, and a costus note give Cabochard its leather character. Interestingly, there is a similarity between Cabochard and Aramis in their use of isobutyl quinoline with the floral-powdery musk ambrette, which is now banned due to safety concerns.

The warmth of its chypre accord is built around patchouli, oakmoss, animalic notes, woody notes of vetiveryl acetate and cedryl acetate, and the amber note of Dynamone, which is a base derived from cistus. The accord is sweetened by methyl ionone. The use of aldehyde C-18 (γ-nonalactone) to lend a soft creamy touch emulates the use of peachy aldehyde C-14 (γ-undecalactone) in earlier chypres like that of Mitsouko (Guerlain, 1919). Spicy notes of cinnamon, clove, and a carnation accord provide a bright contrast to the dusky leathery character. The vegetal musk character of ambrettolide finally echoes the verdant top.

Cabochard is one of the few surviving leather chypre amongst feminine fragrances. Thanks to the brilliance of perfumer Bernard Chant, he extrapolated the iconic leather of Bandit. He softened the leather and gave it verdant florals. The interesting use of materials also gave Cabochard its creative twist and character. It stands on its own as another classic in the family. Although the reformulations may have rendered Cabochard more docile now, but one can still see a glimpse of its complex transformation.

Sources: fragrancex.com, Perfumery Practices and Principles