Reports of Trials for Murder by Poisoning;: by Prussic Acid, Strychnia, Antimony, Arsenic, and Aconita. Including the trials of Tawell, W. Palmer, Dove, Madeline Smith, Dr. Pritchard, Smethurst, and Dr. Lamson, with chemical introduction and notes on the poisons used — John Shaqi
Reports of Trials for Murder by Poisoning;: by Prussic Acid, Strychnia, Antimony, Arsenic, and Aconita. Including the trials of Tawell, W. Palmer, Dove, Madeline Smith, Dr. Pritchard, Smethurst, and Dr. Lamson, with chemical introduction and notes on the poisons usedBrowne, G. Lathom (George Lathom)
Science
Reports of Trials for Murder by Poisoning;: by Prussic Acid, Strychnia, Antimony, Arsenic, and Aconita. Including the trials of Tawell, W. Palmer, Dove, Madeline Smith, Dr. Pritchard, Smethurst, and Dr. Lamson, with chemical introduction and notes on the poisons used
Browne, G. Lathom (George Lathom)
Medical jurisprudence -- Great Britain; Poisons; Trials (Murder) -- Great Britain; Trials (Poisoning) -- Great Britain
The above summary is by no means perfect, since there are minor
differences in each class, which may sometimes rise into such
prominence as to confuse the classification. But in medical evidence
on the individual poisons of which we treat, those physiologically
resembling them in action are always most heard of at the trial, and
questions are asked whether this or that may not produce the same
symptoms; and hence it is well to direct attention to the analogues of
our types.
The primary idea of an _alkaloid_ is derived from its resemblance to
an _alkali_. Alkaloids are often called also “Organic Bases.” Their
names terminate in—_ia_ or _ine_.[2] They are more or less alkaline
to test paper, and combine with acids to form salts which are neutral
in reaction and often crystallizable. Only a few of the alkaloids
are liquid and easily volatile, but almost all can be volatilized
by careful heating at definite temperatures, giving in many cases
a sublimate of characteristic appearance under the microscope,
either of crystals, globules, or a mere film. In a free state, the
alkaloids are very slightly soluble in water, but soluble in alcohol,
and generally in ether and chloroform. Some are soluble in benzine,
others in amylic alcohol, petroleum spirit, acetic ether, &c. On a
judicious use of these various solvents depend the different processes
of isolation, among which Dragendorff’s is the most complete, but so
complicated that it is rarely used in its entirety. Fortunately there
is generally a clue more or less definite to the probable poison
administered, enabling a shorter and quicker method to be adopted. For
further details as to these processes see Blyth’s Manual of Practical
Chemistry. The sulphates, chlorides, and acetates of the alkaloids
are generally soluble in water; if ammonia or potash be added to the
solution, a precipitate (usually crystalline) of the free alkaloid
occurs if the solution be of moderate strength.
Chemically, the alkaloids are derived from ammonia (NH_{3}) by
substituting various organic groups or “compound radicles” (compounds
of carbon and hydrogen), for the hydrogen of the ammonia. They are
therefore “compound ammonias,” or “amines.” Nitrogen, carbon, and
hydrogen, are always present in natural alkaloids, the non-volatile
ones, including the greater number, also contain oxygen.
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