Chronicles of Pharmacy, Vol. 2 (of 2)Wootton, A. C.
History
Chronicles of Pharmacy, Vol. 2 (of 2)
Wootton, A. C.
Pharmacy -- History
Born at Darmstadt, 1829; died at Bonn, 1896.]
But these explanations were by no means sufficient to meet all the
cases which were coming before chemists, and now Kekulé’s brilliant
“closed ring” theory was conceived, and on this most of the wonderful
building up of the synthetic compounds has been planned. Kekulé was
puzzling over the formula C_{6}H_{6} which had been found to represent
benzene, now so famous as the starting point of the aromatic series.
He stated that the solution of the problem came to his mind on the
top of a London omnibus in 1865, when he was an assistant in the
chemical laboratory of St. Bartholomew’s Hospital Medical School. He
conceived the idea of a hexagonal structure with an atom of carbon
at each angle, each united to one atom of hydrogen, and on one side a
double link or bond, and on the other a single one, connecting it with
the next carbon atom, the quadrivalency of each atom being thereby
satisfied.
The formula is depicted in the margin, and is generally accepted; but
it ought to be stated that it has rivals, though all are founded on
the necessity of providing for the saturation of the four links of the
carbon atoms.
H
C
/\\
HC CH
|| |
HC CH
\ //
C
||
ANILINE.
Among the events which gradually led to the production of artificial
compounds for which physiological properties and action have been
claimed, the discovery of aniline is prominent. The substance, now
so well known by that name, was first separated from indigo in 1826
in the course of a dry distillation of that dye by a pharmacist of
Erfurt, named Unverdorben. He named his product “crystalline,” from its
character. In 1834 the same substance, as it was later known to be, was
obtained from coal-tar by Runge, who, observing the violet colour which
bleaching powder caused in its aqueous solution, designated the product
“kyanol.” Ten years subsequently Hofmann continued the investigations
which Runge had pioneered. Meanwhile Fritzsche had obtained anthranilic
acid from indigo, and from that he had produced an oily base which
he called “aniline.” This term was derived from the specific name of
the indigofera anil, which was the Sanskrit designation of the famous
blue dye. Hofmann’s researches ultimately proved that Unverdorben’s
crystalline, Runge’s kyanol, and Fritzsche’s aniline were all
chemically identical. Hofmann would have preferred to retain the first
of these names, but the more definite aniline prevailed.
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