LAVENDER
LAVENDER
Lavender
true; al. Echter Lavendel;
English
. True
lavender
.
Flowering tops.
The real
lavender
is
a
shrub with upright stems unbranched whose top is devoid of leaves. These are green ash, linear. The flowers, with
a
bluish color chalice, are located in the armpit of the bracts with little visible nerviaciones. They are grouped into long thin spikes stalk.
Source
.
The
lavender
genuine,
spontaneous
(In the western Mediterranean basin, is grown in Spain, France and Bulgaria. Its range is similar to that of
lavender
(L. latifolia Medic. which hybrid (lavandin, Interim Emeric L. x ex Loisel.
Chemical composition.
Although the
essential
oil (1 - 3%)
has
resulted in many traditional low, the other components are little known: Ursola acid, flavonoids,
bitter
substances.
Essential
oil. Its composition varies depending on many factors: according to their
origin
(
natural
populations of
lavender
,
lavender
clonal) climatic conditions, the conditions for. The main components of the
essential
oil of
lavender
clonal are: linalol (30 to 40%) and Linalyl acetate (36 to 58%) The cariolifeno (2. 6 to 6. 3%) is provided. The
lavender
from
natural
populations, are poorer in octanone, linalol Linalyl acetate and the
lavender
clonal,
but
are more rich in acetate lavandulilo? Terpineol, beta - ocimene. Have been isolated from other components of santalano of cadinano, and so on. Carbonílicos compounds [695] from cicloadiciones ketones dienófilas on diene (ocimene, mirceno, etc. could participate in its delicate aroma [696]
The
essential
oil of
lavender
is rich in cíñelo (30 - 40%) and
camphor
(15%) compounds that are found in very small quantities in the
essential
oils of lavandin.
Pharmacological data.
Few pharmacological data on the
lavender
, usually, these were the
essential
oil.
Like many other
essential
oils, the
lavender
shows an antimicrobial
activity
observed in vitro with an essentially commercial deterpenada. This
activity
is weaker than that of the
essential
oils of rosemary,
thyme
or
savory
.
The action of
essential
oil on the S. N.
C
.
has
been known since the end of the nineteenth century: narcotic action at small doses (dog, via parenteral) while high doses produced excitement, hallucination, tachycardia and acceleration of breathing. Administered to humans, these same authors observed
a
hypnotic effect (1 g per os) There are also
cardiac
and
respiratory
effects that could assume that the drug
has
sympatholytic properties. There are no known only properties linalol. Those of
camphor
and 1. 8 cineol are better known and could explain some properties attributed to the
essential
oil of
lavender
.
Employment.
Based on the tradition,
now
advises the use of drugs and different preparations based on
lavender
, in the symptomatic treatment of states neurotónicos, especially in cases of sleep
disorders
and as an antispasmodic in case of digestive
disorders
. Via the use of external preparations of
lavender
flowers are advised to clean the skin and as analgesic in
disorders
of the oral cavity and oropharynx, as well as for oral hygiene. The
essential
oil of
moderate
toxicity, is used in aromatherapy and in developing products for use by external: soaps, lotions, creams, disinfectants and healing. The perfume and
cosmetics
also use it for their fragrant and its power bartericida that makes it
a
good preservative. Criomolida the drug does not produce toxic manifestations (acute toxicity tests 3 g / kg and subacute 300 mg / kg / day, rat, per os,
The drug.
The leaves are laceoladas, with the edges rolled and green ash. The flowers are grouped into spikes and loose with bracts bracteolas. The microscopic examination of the
flower
shows TECTOR branched hairs and hairs secreting two types. To be considered official, the oil of
lavender
should contain between 25 and 38% of linalol, between 25 and 45% of Linalyl acetate, and between 0. 2 to 0. 5% and 0. 3 and 1, 5% of
camphor
and cineol respectively. These percentages, as well as those of limonene (0, 1 - 0, 5%) and those of &alfa; terpineol (0, 3 - 1%) are determined by GC.
Bibliography.
The European
Flora
(3, 187 - 188, 1972) indicates that the sinoni -
mia concerns the only subspecies
angustifolia
exists,
Indeed, another subspecies, pyrenaica (DC. Guinea, in the Nord -
I of Spain. On the nomenclature of
lavender
and lavandin.
Flora
is puedeLa Europe (3, 187 - 188, 1972) indicates that the sinoni -
mia concerns the only subspecies
angustifolia
exists,
Indeed, another subspecies, pyrenaica (DC. Guinea, in the Nord -
I of Spain. On the nomenclature of
lavender
and lavandin.
You can also consult the notes of
A
. O. TUCKER:
Botani
-
lime nomenclature of culinary herbs and potherbs, in. Herbs,
spices, and medicinal plants:
recent advances in botany, Horti -
culture and pharmacology, L.
E
. and Crake J.
E
. SIMON ed.
Pho
-
Enix (Arizona) Oryx Press, vol 1, 33 - 80, 1986.
a
) Scientific and Technical Commission of prodarom - Grasse.
et Syndicat des industriels et NEGOCIANTS in
lavender
and lavandin.
française d'origine. Preliminary observation concerning the.
possibility of distinguishing des
lavender
of population of washed -
des (
a
) Scientific and Technical Commission of prodarom - Grasse.
et Syndicat des industriels et NEGOCIANTS in
lavender
and lavandin.
française d'origine. Preliminary observation concerning the.
possibility of distinguishing des
lavender
of population of washed -
Française des clonal.
Parfums,
Cosmetics
. Aroma, 39) 49 - 51, 1981.
b) id. Remarques sur le rapport ß trans - ocimene: octanone -
3 comme critère analytique
essential
oils of
lavender
.
Ann. Fake. Exp. Chim. 74, 409 - 415, 1981.
L. PEYRON.
LAVANDES lavandins et dans le monde.
Parfums,
Cosmetics
. Aroma, 54) 55 - 60, 1983.
A
. O. TUCKER, M. J. MACIARELLO and J.
T
. HOWELL.
A
preliminary analysis of some
lavender
cultivars and lavandin.
Perfume.
Flavor
. 9, 08 - 09) 49 - 52, 1984.
B. M. LAWRENCE.
Progress in
essential
oils:
lavender
oil.
Perfume.
Flavor
. 12, 12 - 87 / 01 - 88) 64 - 70, 1988; see also,
id. ibid. 9, 02 - 03) 48 - 52, 1985.
R. FR. AGNEL and
P
. Teisseire.
Essential
oil of
lavender
french - Its composition and its adult -
ration
.
Perfume.
Flavor
. 9, 10 - 11) 53 - 56, 1984.
R. KAISER and
D
. LAMPARSKY.
New carbonyl compounds in the high - boiling fraction of wash -
der oil.
Helv. FP. Acta, 66, 1843 - 1849, 1983; id. Ibid. 1835 - 1842.
R. KAISER and
D
. LAMPARSKY.
New carbonyl compounds in the high - boiling fraction of wash -
der oil.
Helv. Chim. Acta, 67, 1184 - 1197, 1984.
J. PELLECUER, J. ALLEGRINI, M. Simeon BUOCHBERG.
and J. Passet.
Place de l `essence of Satureia
montana
L. Lips) dans l'arse -
nal Thérapeutiques.
Pl. Méd. Phytother. 9, 99 - 106, 1975.
Lavender
, toxicological dossier
Laboratories
Arkopharma
.
Diseases
whose treatment is appropriate in this plant.
Rhinitis
.
Sinusitis
.
Tracheitis
.
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