Conine

Prof. Filehne, of Erlangen, who has studied a large number of these pyridine and quinoline derivatives, found, moreover, that the hydrochlorate of ethyl-piperidine had a physiological action quite analogous to that of conine. ❋ Various (N/A)

By heating butyl-aldehyde with alcoholic ammonia is formed _paraconine_, an alkaloid isomeric with the natural conine, but differing in physiological action. ❋ Various (N/A)

If a volatile alkaloid, add a few pieces of calcium chloride to ethereal solution to absorb the water; draw off the ethereal solution with a pipette, allow it to evaporate, and test the residue for the alkaloids, conine and nicotine. ❋ Unknown (N/A)

From conine can be prepared methyl-conine, which also occurs in nature, and dimethyl-conine. ❋ Various (N/A)

Piperidine, the decomposition product of piperine, which we have shown may be considered to be hexahydropyridine, was examined by Dr. Kronecker, of Berlin, at the request of Prof. Hofmann, and was found to have an action upon animals in many respects resembling that of conine. ❋ Various (N/A)

The artificial alkaloid paraconine, isomeric with the natural conine, will be referred to later. ❋ Various (N/A)

But with this granted, the simplest alkaloid formulas, those of conine, C_ {8} H_ {17} N, and nicotine, ❋ Various (N/A)

The formula of conine, C_ {8} H_ {17} N, shows it to be homologous with piperidine, C_ {5} H_ {11} N, a derivative of piperine, the alkaloid of pepper, to be spoken of later; and, just as piperidine is derived from pyridine by the action of reducing agents, so conine is probably derived from a propyl-pyridine. ❋ Various (N/A)

Taking up the volatile alkaloids, we find with regard to _conine_, first, that the action of methyl iodide shows it to be a secondary amine, that is, it restrains only one replaceable hydrogen atom of the original ammonia molecule. ❋ Various (N/A)

I had in front of me some of the finest destructive agents you could wish to light upon -- carbon-monoxide, chlorine-trioxide, mercuric-oxide, conine, potassamide, potassium-carboxide, cyanogen -- when Edwards entered. ❋ Richard Marsh (N/A)

Tropine, when heated to 180°C. with concentrated hydrochloric acid, splits off a molecule of water, and yields tropidine, C_ {8} H_ {13} N, a liquid base, with an odor resembling conine. ❋ Various (N/A)

There is ample evidence, I have found, that conine or a substance possessing most, if not all, of its properties is at times actually produced in animal tissues by decomposition. ❋ Unknown (1908)

Was he killed by ordinary ptomaine poisoning, and had conine, or rather its double, developed first in his food along with other ptomaines that were not inert? ❋ Unknown (1908)

"In fact, there would have been no value in it, otherwise, for the experts for the people seem to have established the presence of conine in the body with absolute certainty." ❋ Unknown (1908)

For many animal tissues and fluids, especially if somewhat decomposed, yield not infrequently compounds of an oily nature with a mousey odour, fuming with hydrochloric acid and in short, acting just like conine. ❋ Unknown (1908)

It was testified at the trial that conine, the active principle of hemlock, is intensely poisonous. ❋ Unknown (1908)

An injection of a most minute quantity of real conine will kill a mouse, for instance, almost instantly. ❋ Unknown (1908)

"I find that there is an animal conine as well as the true conine," he hammered out. ❋ Unknown (1908)

Or did the cadaveric conine develop only in the body after death? ❋ Unknown (1908)

Whatever there may have been in the body before, certainly they produced a cadaveric ptomaine conine. ❋ Unknown (1908)