2.6.2 Quantitative Determination of Volatile Oil in a Plant Material
The necessity to determine the
volatile oil quantitatively from a plant material is mostly accomplished by a
specially designed apparatus , which helps in ascertaining the raw material to
be employed for commercial production. Such a determination is also extremely
helpful in establishing and appraising the quality of spices and oleoresins.
Clavenger devised an apparatus
to determine the volatile oils which essentially has several advantages,
namely: (a) Compactness in size, (b) Cohobation of
distillation waters, and (c) Reasonably accurate estimation of
volatile oil content by employing relatively smaller quantum of the raw
material. However, the apparatus also possesses an additional merit for steamrectification
of small quantities of essential oils.
Apparatus It consists of
a round bottomed flask of varying capacity from 1 L to 2 L which is provided
with a hanging type heating mantle and regulator. The mouth of the round
bottomed flask is connected with a specifically designed trap to collect the
volatile oil which could be either heavier than water or lighter than water as
shown in Figure 5.3.
The various vital components of
the apparatus for the quantitative estimation of volatile oils are as
follows:
A = RB–flask,
B = Heating Mantle (Hanging
type),
C = Drug and water
D = Bend insulted with
asbestos/ cotton pad
E = Water condenser
F = Inlet – for water
G = Outlet – for water
H = Volatile oil collected in a
graduated stem
I = Excess water reintroduced
in round bottomed flask
Methodology A known
weight of the drug either as such powdered or cut into small pieces is introduced
into the round bottomed corning flask (1 L or 2 L capacity) along with a
distillation
Fig. 5.3 Apparatus for
Quantitative Estimation of Volatile Oils
medium which often is fresh
water or a mixture of water and glycerin. The quantity of this medium is
usually 3 to 6 times the weight of the drug substance. The distillation is done
for about 5-6 hours.
The distillate is collected in
a specially designed trap (or receiver). The stem of which is graduated upto 5
ml with each ml mark is subdivided into 1/10 the ml. In case, the volatile oil
is heavier than water the trap on the left hand side of Fig. 5.3 is used; and
when the volatile oil is lighter than water the trap on the right hand side is
employed.
Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
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