318 THE CHEMISTEY OF ESSENTIAL OILS
OIL OF AJOWAN SEED.
This oil is the product of distillation of the fruit of the herb
Ptychotis Ajowan (Carum Ajowan), a plant cultivated in many parts of
Egypt, Persia, Afghanistan, and Bengal. The fruit yields from 3 to 4
per cent, of oil. It has the following characters :—
Specific gravity.
Optical rotation.
Refractive index
Phenols
0-910 to 0-930
+ 1° „ + 5°
1-4980 „ 1-6005
45 to 60 per cent
The characteristic odour of the oil is due to the presence of thymol.
In addition, cymene, a-pinene, dipentene, and y-terpinene are present.
The oil itself is used to a certain extent in India for medicinal purposes,
but its principal use is for the preparation of thymol. According to
Stohmann, carvacrol is also present, but this statement requires con-
firmation.
Experimental cultivations of ajowan seed have been made in the
West Indies, but, so far, not on a commercial scale. Ajowan seeds
grown in the Seychelles yield about 9 per cent, of oil containing 38 per
cent, of thymol, and seeds grown in Montserrat yield 3 per cent, of oil
containing 54 per cent, of thymol.^1
OIL OF ANGELICA.
All parts of the herb Angelica officinalis (Angelica Archangelica)
yield essential oils, of which the best known is that distilled from the
fresh root. The plant is a native of Europe, on mountains or river
sides, especially in Lapland, Sweden, Norway, Germany, etc. It is
cultivated to a considerable extent in Saxony, but is comparatively rare
in Britain. Although the root -oil is that mostly used, and held in high
esteem, according to Schimmel & Co. the seed oil is preferable to this.
Angelica root oil is a light yellow or reddish limpid liquid of strong
aromatic odour and pungent taste. The yield from dried roots grown
in the Saxon Erzgebirge is from 0
- 5 to 1 per cent, of oil. The specific
gravity varies from -854 to '918, that from the dried root usually having
a higher specific gravity than that from the fresh root.
The oil has the following characters:—
Specific gravity 0-854 to 0-918
Optical rotation + 16° , + 41°
Refractive index 1-4770 , 1*4880
Acid value 1 , 4
Ester „ 12 , 40
,, ,, (after acetylation) 50 ,, 75
On long standing crystals are deposited, which according to Gior-
dani have the composition C 32 H 62 O 6 , and melt at 74° to 77°. Beilstein
2
showed that the oil contains one or more terpenes. Naudin^3 confirmed
this, and Schimmel & Co. have shown that amongst the lower boiling
fractions of the oil, dextro-phellandrene exists. Ciamician and Silber 4
showed that the crystalline bodies (of which they separated two) exist-
ing in the oil were probably oxyacid anhydrides. Hydrocarbons, prob-
ably sesquiterpenes, were also found, which distilled at 240° to 270°,
(^1) Bull. Imp. Ins*., xvi. 1, 30. (^2) Berichte, 15 (1882), 1741.
»Ibid, 16 (1883), 1382. 4 Ibid., 29 (1896), 1811.