Simple
Flower, Complex Chemistry
The simplicity of a single flower disguises
the complexity of its fragrant aroma. Looking
past its structural beauty, we are awed by thousands
of individual constituents, or ingredients,
as they whirl in perfect order to form a fragrance
that elicits physical, emotional, and even spiritual
responses. Such is the intricate beauty of a
single flower; such is the intricacy of its
essential oils.
Essential oils are very complex in chemical
compounds. Their chemistry, when charted on
paper, boggles the imagination and often leaves
all but the most advanced chemist with feelings
of stupor. One single oil may contain thousands
of individual constituents that exert specific
actions. Take one substance from its normal
surroundings, and combine it with a different
component, and it acts in an entirely different
manner. This makes it quite difficult to define
any constituent's action, for its true action
is often determined by the relationship it has
with all the substances around it. In nature,
no constituent ever works alone, but instead
works in perfect harmony with all the other
ingredients to create a perfect, whole essential
oil.
Nevertheless, for the sake of simplicity, scientists
isolate, observe, and report single actions
and try to identity, name, and categorize individual
components. The essential oils that share a
high proportion of similar constituents are
grouped together and are said to have similar
actions. To help one understand the actions
of the oils, scientists divide the oils' identified
constituents into family units and assign them
names like esters, aldehydes, and phenols.
Oils with a high number of common constituents
tend to mix well with each other when creating
aromatic blends. The effect of essential oils
may be predicted according to the major constituents
present. The identified chemical make-up helps
one discover the potential properties that are
exerted on the physical and mental body. But
once again, this may all change when the single
constituent is blended with new components.
The action of the component may also change
depending on how it is used. Is it inhaled,
rubbed on, or taken internally? How it is taken
helps determine the action of the main constituent.
When mingling with other essential oil users,
you may hear the following terminology. This
chart and glossary will prove useful for the
beginning oil enthusiast, with descriptions
and simplified keys to assist you in peeking
into the complex world of essential oil chemistry.
Common
Constituents Found in Essential Oils:
Esters
Gentle in action, esters are generally found
in the mildest essential oils and are mostly
free of toxicity and irritants. They tend to
be the most relaxing, soothing, and balancing
of all the essential oil constituents. Esters
exert a normalizing effect on imbalances in
emotional and physical conditions. They often
exude a fruity aroma. The names of esters usually
end in -yl, -ate, or -ester.
Names of Common Esters:
linalyl acetate
geranyl acetate
methyl salicylate
Main Effects:
Some are antispasmodic and calming to the nervous
system. Others tend to be antifungal. When applied
topically, some esters exhibit comforting properties
to skin and are soothing for inflamed tissue.
Found in:
lavender,
clary
sage, bergamot,
Roman
chamomile (85%), fir,
and wintergreen.
Aldehydes
Key ingredient to the scent of a plant, aldehydes
exert powerful aromas. Aldehydes are often calming
to the emotions. Essential oils with high aldehyde
content must be used correctly when applied
to the skin as they can cause irritation. The
names of aldehydes usually end in -al,
or -aldehyde.
Names of Common Aldehydes:
geranial
citral
neral
Main Effects:
Calming, antiseptic, antimicrobial; some are
antifungal, and some act as vasodilators.
Found in:
lemongrass,
lemon eucalyptus, lemon verbena, valerian,
and cinnamon
bark.
Ketones
Many ketones are good for the skin and scars.
They are often found in skin care products.
Particular ketones encourage normal cell growth.
The pest-deterring action of marigolds is due
to the ketone, "tagetone." Since various
ketones are resistant to digestion, excessive
usage may cause a buildup in the liver when
taken orally. When used in the context of a
natural, whole essential oil, however, ketones
may be utilized safely. The names of ketones
normally end in -one, but other components
found in essential oils may have the same last
three letters, such as asarone, which
is a phenolic ether, not a ketone.
Names of Common Ketones:
d-pulegone
jasmone
fenchone
isomethone
Main Effects:
Some ketones are soothing to cuts, abrasions,
and irritated tissue; others have lipolytic
(breaks down fat) actions; several ketones are
mucolytic (thins the mucous); while others are
sedative. A number of ketones are analgesic
(for pain). One major action of certain ketones
is that they act as expectorants. Note that
while some ketones are sedative, others are
stimulating.
Found in:
Idaho
tansy, Eucalyptus
dives, spearmint,
hyssop,
Western
red cedar, and sage.
Sesquiterpenes
Sesquiterpenes (as well as a few other constituents)
increase blood flow to the capillaries throughout
the body. They pass the blood brain barrier,
having a positive effect on blood flow to the
brain. They exert a helpful effect on the endocrine
system. Like aldehydes, sesquiterpenes possess
a strong aroma. Though from the same family
of terpenes, sesquiterpenes are larger molecules
than monoterpenes. The names of sesquiterpenes
generally end in -ene.
Names of Common Sesquiterpenes:
b-caryophyllene
germacrene D
aromadendrene
chamazulene
Main Effects:
Antiseptic, antimicrobial, soothing to irritated
skin and tissue, calming; some are analgesic.
Found in:
patchouli,
ginger,
helichrysum,
sandalwood,
cedarwood,
and German chamomile.
Oxides
Oxides are found in a number of essential oils,
mainly those that have a camphor-like nature.
The most common oxide in aromatherapy is l,8-cineole-a
strong expectorant. For example, the smell of
fresh-baked bread is due to an oxide. The names
of oxides generally end in -oxide.
Names of Common Oxides
1,8-cineole
bisabolol oxide
linalool oxide
sclareol oxide
Main effects:
Expectorant; mildly stimulating.
Found in:
Eucalyptus
globulus, rosemary,
ravensara,
and German chamomile.
Monoterpenes
Monoterpenes make up the largest single class
of compounds found in essential oils (see chart).
They generally possess antibacterial agents.
Monoterpenes in general have a stimulating effect.
Terpenes are light molecules that normally evaporate
quickly. A terpene is insoluble in water and
is often removed from perfume since it causes
cloudiness. The names of all terpenes end in
-ene.
Names of Common Terpenes:
d-limonene
myrcene
p-cymene
Main effects:
Antiseptic; soothing to irritated tissue; limonene
is believed to be antitumerol; some monoterpenes
are analgesic.
Found In:
grapefruit,
frankincense,
orange,
thyme,
and balsam
fir.
Alcohols
Not to be confused with grain alcohols, this
plant constituent is somewhat stimulating and
helps to increase blood circulation. Some alcohols
decrease blood thickness without being over-thinning.
Alcohols are very resistant to oxidation and
have a very low toxicity. Non-phenolic alcohols
are mild and possess pleasant floral odors.
Phenolic alcohols, on the other hand, are very
strong and aggressive and can be irritating
to the skin. The names of alcohols usually end
in –ol.
Names of Common Alcohols:
borneol
terpineol
geraniol
Main effects:
Strongly antimicrobial; some are uplifting,
while others are sedative; used in animal studies
to revert cells to normal function and activity.
Found in:
rosewood,
coriander,
geranium,
rose,
and lavender.
Phenols
Phenols are a type of alcohol. Phenols are highly
subject to oxidation and darken or redden with
age. Only four common phenols are found in essential
oils: thymol, carvacrol, eugenol, and chavicol.
They are typically considered medicinal in character.
Phenols often smell pungent and spicy. They
are helpful for poor moods and for healing.
Many are irritating to the skin when used incorrectly.
The names of most phenols end in -ol, which
may be confusing since alcohols also end in
–ol.
Names of Common Phenols:
thymol
eugenol
chavicol
Main Effects:
Antiseptic, powerful anti-microbial; stimulating
to the nervous and the immune systems; uplifting;
many are irritating to the skin, but some have
an opposite effect.
Found In:
wintergreen,
clove,
cinnamon,
thyme,
oregano,
and peppermint.
Main
Chemical Constituents of Young Living's Single
Oils
You
may find some discrepancies caused by growing
conditions, amount of water the plant received,
when it was harvested, etc. For each oil, the
three main constituents are marked by a colored
check. The means
there is more of, or a significant amount of
that particular substance. The indicates
a lesser but still significant amount of that
particular constituent.
| Oil
Common Name |
Botanical
Name |
Esters |
Alde-
hydes |
Ketones |
Sesqui-
terpenes |
Oxides |
Monoter-
penes |
Alcohols |
Phenols |
|
Ocimum
basilicum |
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Citrus
bergamia |
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Cedrus
atlantica |
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Chamaemelum
nobile |
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Cinnamomum
verum |
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Cistus
ladanifer |
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Salvia
sclarea |
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Syzgium
aromaticum |
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Coriandrum
sativum |
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Cupressus
sempervirens |
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Anethum
graveolens |
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Canarium
luzonicum |
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Eucalyptus
Dives |
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Eucalyptus
Globulus |
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Eucalyptus
Polybractea |
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Eucalyptus
Radiata |
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Foeniculum
vulgare |
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Abies
balsamea |
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Pseudotsuga
menziesii |
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Abies
concolor |
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Boswellia
carteri |
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Galbanum |
Ferula
gummosa |
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Pelargonium
graveolens |
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Zingiber
officinale |
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Solidago
canadensis |
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Citrus
paradisi |
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Helichrysum
officinalis |
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Hyssopus
officinalis |
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Jasminum
officinale |
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Juniperus
osteosperma & Juniperus scopulorum |
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Laurus
Nobilis |
Laurus
Nobilis |
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Lavandula
angustifolia |
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Ledum
groenlandicum |
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Citrus
limon |
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Cymbopogon
flexuosus |
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Origanum
majorana |
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Melaleuca
alternifolia |
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Melaleuca
ericifolia |
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Melissa
officinalis |
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Satureja
montana |
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Commiphora
myrrha |
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Myrtus
communis |
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Myristica
fragrans |
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Citrus
sinensis |
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Origanum
compactum |
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Pogostemon
cablin |
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Piper
nigrum |
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Mentha
peperita |
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Petitgrain |
| |