Cocain Chemische Eigenschaften,Einsatz,Produktion Methoden
R-S?tze Betriebsanweisung:
R23/24/25:Giftig beim Einatmen, Verschlucken und Berührung mit der Haut.
R43:Sensibilisierung durch Hautkontakt m?glich.
S-S?tze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn m?glich, dieses Etikett vorzeigen).
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S22:Staub nicht einatmen.
Beschreibung
Cocaine is best known as an illegal drug that produces a euphoric “high” in individuals who
use it. Cocaine is an alkaloid obtained from the leaves of the coca plant, Erythroxylum coca,
which is native to northwestern South America and Central America.
Chemische Eigenschaften
Cocaine (also known as methylbenzoylepgonine), C17H21NO4, is a colorless-to-white crystalline substance, usually reduced to powder. Cocaine is soluble in alcohol, chloroform, and ether, slightly soluble in water, giving a solution slightly alkaline to litmus.
Physikalische Eigenschaften
Appearance: pure white crystal, odorless. Solubility: insoluble in water (1:600);
soluble in chloroform (1:0.7), ethyl ether (1:3), ethanol (1:7), and other organic
solvents; soluble in acetone, benzene, ethyl acetate, two carbonyl sulfide, and petroleum ether; show monoclinic flaky crystal in ethanol. Melting point: 98° (it can
be slowly evaporated over 90°), the specific rotation of ?16°.
History
In 1855, cocaine was first extracted from the leaves of herbal ingredients and named
Erythroxylon by the German chemist Friedrich (G. Friedrich) (1828–1890). In
1859, the German chemist Niemann (Albert Niemann) (1834–1861) defined a
higher purity of material, named cocaine. In 1880, cocaine was used as a local
anesthetic by the “father of modern surgery,” William Stewart Halsted. In 1884,
cocaine was firstly recommended to be used as a local anesthetic, sexual stimulant,
and antidepressant by Sigmund Freud, a famous psychologist in Austria (1856–
1939). He called it “a magical substance”
Verwenden
Use of cocaine is known since early times.It occurs in the South American coca leaves.Chewing of leaves mixed with lime was acommon practice among natives, who traveledgreat distances without experiencingfatigue (Cordell 1978). Cocaine is obtainedby extraction of coca leaves. It is also preparedby methylation and benzoylation of thealkaloid, ecgonine. The dilute aqueous solutionsof its hydrochloride is used as a topicalanesthetic in ophthalmology. Cocaine and itsderivatives are controlled substances listedin the U.S. Code of Federal Regulations(Title 21, Parts 321.1 and 1308.12, 1987).
Definition
cocaine: A powerful drug present inthe leaver of the coca plant (Erythroxyloncoca). It stimulates the centralnervous system and has effects similarto the amphetamines. It was originallyused as a local anaesthetic. Theillegal drug is usually the soluble hydrochloride.This can be convertedinto the free-base form (known ascrack cocaine) by dissolving in waterand heating with sodium bicarbonate.Cocaine is a class A drug in theUK. It can be detected by Scott’stest.
Vorbereitung Methode
Colombia is the world’s leading producer of cocaine, with about 75% of the world’s production.Coca is grown locally and is also imported from Peru and Bolivia.the processing of coca involves mashing the leaves with a base, kerosene, and sulfuric acid to produce a pastecontaining between 40% and 70% cocaine. It can then be exported where it is dried andpurified into cocaine hydrochloride. Estimates of global consumption of cocaine vary, but areasonable approximation is roughly 750 tons. Of this amount, approximately one-third isimported into the United States, which is the leading consumer of cocaine.
Indications
It is mainly used for local anesthesia in various operations. It is also suitable for
nasal, pharyngeal, ear, urethra, vagina, and other operations (with 5–10% solution).
2% to 3% solution is used for eye surgery.
Allgemeine Beschreibung
Cocaine as a euphoriant–stimulant, psychotomimetic, anddrug of abuse could as well be discussed with amphetamineand methamphetamine, with which it shares many biologicalproperties. At low doses, it produces feelings of well-being,decreased fatigue, and increased alertness. Cocaine tends toproduce compulsive drug-seeking behavior, and a full-blowntoxic psychosis may emerge. Many of these effects appear tobe related to the effects of increased availability of DA for interactionwith postsynaptic receptors (D
2 and D
3 receptors arepertinent). Cocaine is a potent DA reuptake blocker, acting bycompetitive inhibition of the DAT. A phenethylamine moiety with added steric bulk may suffice for this action. An interactionbetween a hydrogen atom on the nitrogen of the protonatedform of cocaine and an oxygen of the benzoyl estergroup, or alternatively, an interaction between the unsharedelectron pair of the freebase nitrogen and the carbonyl of thebenzoyl ester group, could approximate this moiety.
Hazard
Poison; powerful central nervous system
effects.
Mechanism of action
Cocaine has been shown to block the reuptake of norepinephrine, serotonin, and dopamine; however, the reinforcing
and stimulant nature of cocaine seems to be related primarily to blockade of dopamine reuptake, leading to the
“ dopamine hypothesis” of cocaine's actions. [3H]Cocaine was used in an attempt to identify the “cocaine
receptor,” and this was later shown to be similar to the dopamine transporter. Currently, it is thought that cocaine
produces it reinforcing effects by interfering with dopamine reuptake by blocking the dopamine
transporter. Although the human dopamine transporter has been cloned, it is unknown if the dopamine and
cocaine binding domains are identical or how much they overlap.
Clinical Use
Cocaine has a very interesting history. The coca plant was used by South American Indians for religious and
mystical purposes and as a stimulant both to increase endurance and to alleviate hunger. It was introduced into
Europe during the 1800s, and at the end of the 19th century, cocaine use was popular and socially acceptable.
Various cocaine-containing preparations were available, and it also was used to “fortify” wines (e.g., Vin Coca). For
a period of approximately 20 years, until just after the turn of the century, it was a constituent of the soft drink
Coca-Cola. Additionally, cocaine was used for therapeutic reasons but was later supplanted by amphetamine.
Sicherheitsprofil
A human poison by
ingestion and possibly other routes. Poison
experimentally by ingestion, intraperitoneal,
intravenous, subcutaneous, and parented
routes. Human central nervous system
effects by ingestion and possibly other
routes: general anesthesia, hallucinations or
distorted perceptions, and convulsions. An
eye irritant. A widely abused, controlled
substance. Abuse leads to habituation or
addiction. In medcine, it is used as a local
narcotic anesthetic applied topically to
mucous membranes. The free base is solublein fats and thus is used for ointments and
oily solutions. For water-soluble
applications, the sulfate or hydrochloride is
used. See also ESTERS. When heated to
E decomposition it emits highly toxic fumes.
Stoffwechsel
Cocaine is active via nearly every possible route of administration; however, insufflation of “snow” or “coke”
represents one of the most popular routes. Administered in this manner, peak effects and plasma levels are achieved
within 30 minutes. Smoking the freebase form of cocaine (“crack”) results in an even more rapid effect. The
freebase form rather than the hydrochloride salt is used for smoking, because the temperatures required for
vaporization of the salt result in considerable decomposition. Intravenously administered cocaine can achieve
peak blood levels within a few minutes. Cocaine is metabolized to benzoylecgonine, the methyl ester of ecgonine,
and to a lesser extent, to ecgonine, norcocaine, and hydroxylated derivatives.
l?uterung methode
()-Cocaine crystallises from EtOH and sublimes below 90o in a vacuum in an amorphous form. The hydrochloride crystallises from MeOH/Et2O with m 195o and [] D20 -72o (c 2 in H2O, pH 4.5), -78.5o (50% aqueous EtOH). [Sam & Reynolds J Chem Soc 97 1335 1910, Tufariello et al. J Am Chem Soc 101 2435 1979.] -Cocaine is the (+) enantiomer. [Beilstein 22 I 547, 22 II 150.]
Einzelnachweise
Palit, Khare, Phytochem., 8, 1559 (1969)
Cocain Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
