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DELTA9-TETRAHYDROCANNABINOL

DELTA9-TETRAHYDROCANNABINOL Struktur
1972-08-3
CAS-Nr.
1972-08-3
Englisch Name:
DELTA9-TETRAHYDROCANNABINOL
Synonyma:
THC;Dronabinol;TETRAHYDROCANNABINOL;Hashish;72-08-3;Marinol;DELTA-9-THC;(-)-delta9-trans-Tetrahydrocannabinol;(-)-delta(sup9)-trans-Tetrahydrocannabinol;EXO-THC
CBNumber:
CB0199241
Summenformel:
C21H30O2
Molgewicht:
314.46
MOL-Datei:
1972-08-3.mol

DELTA9-TETRAHYDROCANNABINOL Eigenschaften

Schmelzpunkt:
<25 °C
alpha 
D20 -150.5° (c = 0.53 in CHCl3)
Siedepunkt:
bp0.02 200°
Dichte
1.0536 (rough estimate)
Brechungsindex
1.5404 (estimate)
Flammpunkt:
14 °C
storage temp. 
2-8°C
Aggregatzustand
ethanol solution
pka
pKa 10.6 (Uncertain)
Wasserl?slichkeit
2.8mg/L(23 ºC)
BCS Class
2/4
CAS Datenbank
1972-08-3
EPA chemische Informationen
Tetrahydrocannabinol (1972-08-3)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher F,T
R-S?tze: 11-39/23/24/25-23/24/25
S-S?tze: 16-7-45-36/37
RIDADR  UN 1230 3/PG 2
WGK Germany  1
HazardClass  6.1(b)
PackingGroup  III
Giftige Stoffe Daten 1972-08-3(Hazardous Substances Data)
Toxizit?t LD50 (sesame oil emulsion) in male rats (mg/kg): 800 orally; 35.5. i.v.; 672 i.p. (Rosenkranz)
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H225 Flüssigkeit und Dampf leicht entzündbar. Entzündbare Flüssigkeiten Kategorie 2 Achtung GHS hazard pictogramssrc="/GHS02.jpg" width="20" height="20" /> P210,P233, P240, P241, P242, P243,P280, P303+ P361+P353, P370+P378,P403+P235, P501
H370 Sch?digt die Organe. Spezifische Zielorgan-Toxizit?t (einmalige Exposition) Kategorie 1 Achtung GHS hazard pictogramssrc="/GHS08.jpg" width="20" height="20" /> P260, P264, P270, P307+P311, P321,P405, P501
Sicherheit
P210 Von Hitze, hei?en Oberfl?chen, Funken, offenen Flammen und anderen Zündquellenarten fernhalten. Nicht rauchen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P370+P378 Bei Brand: zum L?schen verwenden.
P403+P235 An einem gut belüfteten Ort aufbewahren. Kühl halten.

DELTA9-TETRAHYDROCANNABINOL Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R11:Leichtentzündlich.

S-S?tze Betriebsanweisung:

S16:Von Zündquellen fernhalten - Nicht rauchen.
S7:Beh?lter dicht geschlossen halten.

Beschreibung

Tetrahydrocannabinol (THC) is the main active compound in marijuana. It comes from the plant Cannabis sativa (cannabis), which is a dioecious (monoecious varieties do exist) annual herb naturally found in many tropic and temperate regions of the world. Many varieties of cannabis exist, and two related species (Cannabis indica and Cannabis ruderalia) are main sources of THC. Cannabis sativa is also known as hemp, although this name is not unique to the species; its stem is a source of fiber that has been used throughout history for hundreds of applications including rope, twine, paper, and cloth. Hemp seeds are edible and high in protein. The seeds are also a source of fatty oil that can be used for food, cosmetics, medicines, and as a fuel source. Cannabis contains chemicals called cannabinoids; of the 60 cannabinoids found in Cannabis, one is THC, , which is the psychoactive ingredient in marijuana. Marijuana is produced from the leaves and fl owers of cannabis, and hashish is a resin collected from the female fl owers. The THC content, which determines the effect of cannabis drugs, varies with plant structure, variety, and preparation. Buds and fl owers specifically cultivated for drug use have greater THC content than leaves. THC content may vary from a few tenths of a percent to more than 10%, but good quality marijuana has a THC content of approximately 10%, and good hashish and hashish oils generally have THC contents between 30% and 80%.

Chemische Eigenschaften

Thick Brown Oil

History

THC was first isolated from hashish in 1964 by Raphael Mechoulam (1930–) and Yehiel Gaoni at the Weizmann Institute. In the early 1990s, the specific brain receptors affected by THC were identified. These receptors are activated by a cannabinoid neurotransmitter called arachidonylethanolamide, known as anandamide. Anandamide was named by Mechoulam using ananda, which is the Sanskrit word for ecstasy. Anandamide is thought to be associated with memory, pain, depression, and appetite. THC is able to attach to and activate anandamide receptors. These receptors are actually called THC receptors rather than anandamide receptors because researchers discovered that THC attaches to these receptors before anandamide was discovered. The areas of the brain with the most THC receptors are the cerebellum, the cerebral cortex, and the limbic system. This is why marijuana affects thinking, memory, sensory perception, and coordination.

Verwenden

It is the principal active constituent of cannabis. Agonist at CB1 and CB2 cannabinoid receptors. Antiemetic; appetite stimulant. Controlled substance (hallucinogen).

Definition

ChEBI: A diterpenoid that is 6a,7,8,10a-tetrahydro-6H-benzo[c]chromene substituted at position 1 by a hydroxy group, positions 6, 6 and 9 by methyl groups and at position 3 by a pentyl group. The principal psychoactive constituent f the cannabis plant, it is used for treatment of anorexia associated with AIDS as well as nausea and vomiting associated with cancer chemotherapy.

Allgemeine Beschreibung

Brown amorphous semi-solid, viscous oil or chunky golden yellow solid.

Air & Water Reaktionen

Slightly soluble in water.

Reaktivit?t anzeigen

DELTA9-TETRAHYDROCANNABINOLis very unstable to light and high temperatures. DELTA9-TETRAHYDROCANNABINOL should be protected from air during all handling due to its extreme instability. . Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides.

Brandgefahr

Flash point data for DELTA9-TETRAHYDROCANNABINOL are not available; however, DELTA9-TETRAHYDROCANNABINOL is probably combustible.

Biologische Aktivit?t

Cannabinoid receptor agonist (K i values are 5.05 and 3.13 nM for CB 1 and CB 2 receptors respectively; EC 50 values are 6, 0.4 and 8 nM at CB 1 , CB 2 and GPR55 receptors respectively). Major psychoactive constituent of marijuana.

Clinical Use

Dronabinol (synthetic △9-THC) i s a n antinauseant approved for the treatment of nausea and vomiting associated with cancer chemotherapy in patients who have failed to respond adequately to conventional antiemetics. A related cannabinoid, nabilone, was introduced in Canada for his indication in 1982.

Sicherheitsprofil

Poison by intraperitoneal and intravenous routes. Moderately toxic by ingestion. Experimental reproductive effects. Questionable carcinogen with experimental tumorigenic and teratogenic data. Human mutation data reported. A hallucinatory drug. When heated to decomposition it emits acrid smoke and irritating fumes. See also CANNABIS.

DELTA9-TETRAHYDROCANNABINOL Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

1972-08-3()Verwandte Suche:


  • (-)-trans-DELTA1-Tetrahydrocannabinol
  • (-)-trans-delta9-Tetrahydrocannabinol
  • (-)-trans-DELTA9-THC
  • (6aR,10aR)-6a,7,8,10a-Tetrahydro-6,6,9-trimethyl-3-pentyl-6H-dibenzo[b,d]pyran-1-ol
  • (l)-delta1-Tetrahydrocannabinol
  • 14C-delta1-Tetrahydrocannabinol
  • 1-trans-delta(sup9)-tetrahydrocannabinol
  • 6,6,9-Trimethyl-3-pentyl-7,8,9,10-tetrahydro-6H-dibenzo(b,d)pyran-1-ol
  • 6H-Dibenzo(b,d)pyran-1-ol, 6a,7,8,10a-tetrahydro-6,6,9-trimethyl-3-pentyl-
  • 6H-Dibenzo(b,d)pyran-1-ol, 6a,7,8,10a-tetrahydro-6,6,9-trimethyl-3-pentyl-, trans-
  • 6H-Dibenzo[b,d]pyran-1-ol, 6a,7,8,10a-tetrahydro-6,6,9-trimethyl-3-pentyl-, (6aR-trans)-
  • 6H-Dibenzo[b,d]pyran-1-ol, 6a,7,8,10a-tetrahydro-6,9,9-trimethyl-3-pentyl-, (6ar-trans)-
  • Abbott 40566
  • Cannabinol, 1-trans-delta(sup9)-tetrahydro-
  • Cannabinol, delta1-Tetrahydro-
  • delta(sup9)-Thc
  • delta1-THC
  • delta9-trans-Tetrahydrocannabinol
  • trans-(9)-Tetrahydrocannabinol
  • 9-trans-Tetrahydrocannabinol
  • (-)-DELTA9-TETRAHYDROCANNABINOL
  • DELTA9-TETRAHYDROCANNABINOL
  • (-)-DELTA-9-THC
  • DELTA 9 THC, (-)-
  • DELTA1-TETRAHYDROCANNABINOL
  • Δ1-Tetrahydrocannabinol, Δ9-THC
  • (-)-trans-Δ9-THC
  • (6aR)-6aβ,7,8,10aα-Tetrahydro-6,6,9-trimethyl-3-pentyl-6H-dibenzo[b,d]pyran-1-ol
  • (6aR,10aR)-6,6,9-Trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-dibenzo[b,d]pyran-1-ol
  • Δ1-3,4-trans-tetrahydrocannabinol
  • Δ9-Tetrahydrocannabinol solution,Δ1-Tetrahydrocannabinol
  • Methanol(test (-)-delta9-THC, 1.0 mg/Ml)
  • (-)-δ9-THC
  • (?)-Δ9-THC solution
  • (-)-trans-D9-Form
  • Exocyclic delta(9)(11)-Tetrahydrocannabiol
  • L-delta1-trans-Tetrahydrocannabinol
  • L-trans-delta9-Tetrahydrocannabinol
  • NSC-134454
  • QCD 84924
  • SP 104
  • trans-delta9-Tetrahydrocannabinol
  • (-)-DELTA9-TETRAHYDROCANNABINOL >95% 10M G/ML IN ETHANOL
  • DELTA9-TETRAHYDROCANNABINOL ETHANOL*SOLU TION--DEA S
  • Δ-9-Tetrahydrocannabinol
  • △1-tetrahydrocannabinol
  • △9-tetrahydrocannabinol solution
  • Δ1-tetrahydrocannabinol
  • Δ9-tetrahydrocannabinol solution
  • THC ELISA
  • 1-TRANS-DELTA9-TETRAHYDROCANNABINOL
  • 1-trans-D9-Tetrahydrocannabinol
  • 3-pentyl-6,6,9-trimethyl-6a,7,8,10a-tetrahydro-6H-dibenzo[b,d]pyran-1-ol
  • 6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-dibenzo[b,d]pyran-1-ol
  • 6H-Dibenzo
  • 9-delta-Tetrahydrocannabinol
  • Cannabis resin
  • delta(sup 1)-thc
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