Food Adulteration and Its Detection: With photomicrographic plates and a bibliographical appendixBattershall, Jesse P. (Jesse Park)
Science
Food Adulteration and Its Detection: With photomicrographic plates and a bibliographical appendix
Battershall, Jesse P. (Jesse Park)
Food adulteration and inspection; Food adulteration and inspection -- United States
The presence of fusel oil in liquors is sometimes quite readily
detected, by first removing the ethylic alcohol by gentle evaporation,
and then inspecting the odour and taste of the still warm residue.
The suspected liquor may also be agitated with an equal volume of
ether, water added, and the ethereal stratum removed by means of a
pipette, and concentrated by evaporation; the residue is to be examined
for amylic alcohol. When distilled with a mixture of sulphuric and
acetic acids, amylic alcohol is converted into amylic acetate, which
may be recognised by its characteristic pear-like odour; or, the
amylic alcohol can be transformed into valerianic acid (which also
possesses a distinctive odour) by oxidation with sulphuric acid and
potassium dichromate. Another simple qualitative test for fusel oil
consists in first decolorising a small quantity of the liquor under
examination with animal charcoal, adding a few drops of hydrochloric
acid, and then a little freshly distilled and colourless aniline
oil, when, in presence of fusel oil, it will be observed that the
aniline compound acquires a perceptible rose tint as it falls to the
bottom of the liquid. The quantitative determination of fusel oil
presents some difficulties. A very ingenious method has been suggested
by Marquardt.[118] It consists essentially in first agitating the
sample with chloroform, draining off the solution obtained, washing
it by repeated shaking with water, and then treating it at 85° with a
mixture of 5 parts potassium dichromate, 2 parts sulphuric acid, and
30 parts of water. The valerianic acid thus formed is now separated
by distilling the mixture of water and chloroform. The distillate is
digested with barium carbonate, next concentrated by evaporation,
and then filtered, and divided into two equal portions. One portion
is evaporated to dryness, the residue taken up with water containing
a little nitric acid, and the amount of barium present determined
by precipitation with sulphuric acid. In the other portion, the
chlorine originating from a partial oxidation of the chloroform, is
to be estimated. The amount of barium combined with the chlorine, is
deducted from the total quantity obtained; the remainder represents the
proportion in combination with the fatty acids formed by oxidation. Of
these, valerianic acid largely predominates; and the amount of barium
valerianate [Ba_{2} (C_{2}H_{3}O_{2})] found is calculated to its
equivalent in amylic alcohol. Capsicum, creosote, etc., are isolated by
treating the sample with ether or benzole, and testing the odour and
taste of the evaporated solutions so prepared.
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