A practical treatise on the manufacture of perfumery : $b comprising directions for making all kinds of perfumes, sachet powders, fumigating materials, dentrifices, cosmetics, etc., etc., with a full account of the volatile oils, balsams, resins, and other natural and artificial perfume-substances, including the manufacture of fruit ethers, and tests of their purityDeite, C. (Carl)
History
A practical treatise on the manufacture of perfumery : $b comprising directions for making all kinds of perfumes, sachet powders, fumigating materials, dentrifices, cosmetics, etc., etc., with a full account of the volatile oils, balsams, resins, and other natural and artificial perfume-substances, including the manufacture of fruit ethers, and tests of their purity
Deite, C. (Carl)
Cosmetics; Perfumes; Perfumes industry
According to a notice published in the "Deutsch-Amerikanischen
Apotheker Zeitung," vanillin adulterated with benzoic acid has occurred
in the United States. A sample subjected to examination is said to
have been nothing but benzoic acid perfumed with vanillin. Such an
adulteration can be detected with the microscope, since vanillin
crystallizes in acicular crystals, and benzoic acid in lamina, which
can be readily recognized. Pure vanillin melts at 176° F., while
the melting points of such mixtures are considerably higher, it
being in one case at 249° F. By extracting such mixture with thin
sodium carbonate solution, benzoic acid passes into solution. After
neutralizing with hydrochloric acid, the filtrate yields with ferric
chloride a fawn-brown precipitate of ferric benzoate, and on adding
hydrochloric acid in excess, the benzoic acid, which dissolves
with great difficulty in cold water, is precipitated. By treating
the latter, or the ferric benzoate, with dilute sulphuric acid and
magnesium, the benzoic acid is reduced to benzaldehyde, which is
recognized by its characteristic odor of oil of bitter almonds.
_Nitrobenzol_ is obtained by treating benzol, or a mixture of it,
with toluol and their higher homologues, with strong nitric acid,
or a mixture of nitric and sulphuric acids, washing the product of
reaction with water and soda, caustic soda or ammonia, expelling the
unaltered hydrocarbons with steam and rectifying the residue. Three
varieties distinguished by their boiling points and odor occur in
commerce. The nitrobenzol or oil of mirbane (_essence de mirbane_) is
the so-called _light nitrobenzol_, which boils at from 401° to 415° F.
The _heavier_ varieties boil at a higher temperature and have a more or
less disagreeable odor; they are used in the manufacture of aniline and
aniline colors.
Pure oil of mirbane is pale yellow, the finest qualities being
colorless and almost as clear as water. It has an agreeable odor
resembling that of oil of bitter almonds, a specific gravity of 1.186
to 1.2 = 25° Bé., and congeals at 37.4° F. to a crystalline mass. It is
scarcely soluble in water, sparingly so in alcohol and with difficulty
in watery spirit of wine; it is miscible in all proportions with ether,
benzine, volatile oils, and most fat oils.
Oil of mirbane is largely manufactured in England, but the German
product is now generally preferred, it being purer and does not impart
to soap perfumed with it a yellowish tinge. The finest oil of mirbane
is prepared from pure crystallizable benzol, and again purified
by washing with potassium bichromate and sulphuric acid, and by
rectification with steam.
Pure nitrobenzol suffers no change by boiling with soda lye, while the
poorly rectified product colors the lye yellow or brown.
Public-domain text, read in full here on John Shaqi.
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