Chemistry of Essential Oils

(Tuis.) #1

COMPOSITE 303


The known constituents of the oil are the terpene, limonene, terpineol,
and traces of citronellal.

OIL OF ELECAMPANE.

This oil is distilled from the roots of Inula helenium, a plant indi-
genous to Southern Asia and Siberia, and found to a fair extent in
Southern Europe and North America. The oil has the following
characters :—
Specific gravity 1-013 to 1-0380
Optical rotation + 120 to + 123° 45'
Refractive index ....... 1 * 5220
Acid value 6 to 8
Ester ,„ 160 „ 180
„ „ (after acetylation) .... 186 „ 199
The oil is semi-solid, owing to the deposition of crystals of alantolactone,
the above specific gravities being those taken in the superfused condi-
tion. The principal constituent of the oil is alantolactone, with small
quantities of alantic acid, alantol, and helenin (which is probably identical
OH
/
with isoalantolactone). Alantie acid has the formula CUH 20 , and

COOH
alantol is isomeric with camphor C 10 H 16 O.

OIL OF CHRYSANTHEMUM JAPONICUM.

The leaves and flowers of this plant yield an essential oil which is
known in Japan as kiku oil. It has a specific gravity about 0*885 and
boils at 165° to 175°. According to Perrier,
1
the green leaves of the
plant yield an oil of specific gravity 0*932 and refractive index 1*4931.
It contains a paraffin hydrocarbon, and probably angelic acid in the
form of esters.

OIL OP CHRYSANTHEMUM CINBRARI^EFOLIUM.

The flowers of this plant, growing largely in Dalmatia and Monten-
egro, and which, when ground, form the insect powder of commerce,
yield about 0 07 per cent, of essential oil. According to Siedler,^2 it con-
tains a paraffin C 1 4H3 0 melting at 54° to 56° and a substance melting at
62°, probably palmitic acid. It also contains a phenol, and probably
butyric acid.
OIL OP CHRYSANTHEMUM MARGINATUM.

Shinosaki^3 has obtained 0*005 per cent, of a greenish blue essential
oil by distilling this plant. The oil has the following characters :—


Specific gravity 0*923 at 15°
Optical rotation - 46'58°
Refractive index 1*5020 at 20°
Saponification value 16*3
„ „ (after acetylation) .... 63-1

(^1) Butt. Soc. Chim., iii. 23 (1900), 216.



  • Ber. d. deutsch. Pharm. Ges., 25 (1915), 297.
    *J. Chem. Ind. Tokyo (1919), 22, 455.

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