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T-047

Supelco

(±)-Δ9-THC solution

100 μg/mL in heptane, ampule of 1 mL, Cerilliant®

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About This Item

Wzór empiryczny (zapis Hilla):
C21H30O2
Numer CAS:
6465-30-1
Masa cząsteczkowa:
314.46
Numer WE:
205-563-8
Kod UNSPSC:
41116107
NACRES:
NA.24

Poziom jakości

300

Formularz

liquid

Właściwości

Snap-N-Spike®/Snap-N-Shoot®

opakowanie

ampule of 1 mL

producent / nazwa handlowa

Cerilliant®

drug control

Narcotic Licence Schedule D (Switzerland); psicótropo (Spain); Decreto Lei 15/93: Tabela IIB (Portugal)

stężenie

100 μg/mL in heptane

metody

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

Zastosowanie

cannabis testing
cannabis testing

Format

single component solution

temp. przechowywania

−20°C

InChI

1S/C21H30O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h11-13,16-17,22H,5-10H2,1-4H3

Klucz InChI

CYQFCXCEBYINGO-UHFFFAOYSA-N

Powiązane kategorie

Opis ogólny

(±)-Δ9-THC is the main active constituent and the primary psychoactive cannabinoid of cannabis. Besides persistent illicit use this drug is suitable as treatment for anorexia and nausea and is sold under the trade name Marinol®. This Certified Spiking Solution® is suitable as starting material in calibrators or controls for a variety of LC/MS or GC/MS applications from forensic analysis and clinical toxicology to urine drug testing.

Zastosowanie


  • Drug Release from Polymeric Nanoparticles: Ethyl acetate′s role was highlighted in the modulation of drug release behaviors from poly(lactic-co-glycolic acid) nanoparticles, illustrating its applicability in pharmaceutical formulations (Wang et al., 2024).

  • Preparative Isolation of Alkaloids: A method for the isolation and purification of alkaloids from Gelsemium was developed using ethyl acetate, enhancing high speed counter-current chromatography and preparative HPLC techniques (Liang et al., 2024).

  • Antimicrobial Strain Characterization: Ethyl acetate was utilized in the isolation and characterization of Bacillus subtilis strain O-741, demonstrating its effectiveness against Vibrio parahaemolyticus and potential for broad biomedical applications (Chen et al., 2024).


Inne uwagi

For Qualitative Use Only

Informacje prawne

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
CERTIFIED SPIKING SOLUTION is a registered trademark of Cerilliant Corporation
Marinol is a registered trademark of Unimed Pharmaceuticals, Inc.
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany
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Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

H225,H304,H315,H336,H410

Zwroty wskazujące środki ostrożności

P210 - P233 - P273 - P301 + P310 - P303 + P361 + P353 - P331

Klasyfikacja zagrożeń

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Organy docelowe

Central nervous system

Kod klasy składowania

3 - Flammable liquids

Klasa zagrożenia wodnego (WGK)

WGK 2

Temperatura zapłonu (°F)

24.8 °F - closed cup

Temperatura zapłonu (°C)

-4 °C - closed cup

Wybierz jedną z najnowszych wersji:

Certyfikaty analizy (CoA)

Lot/Batch Number

Przepraszamy, ale COA dla tego produktu nie jest aktualnie dostępny online.

Proszę o kontakt, jeśli potrzebna jest pomoc Obsługa Klienta

Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

David R Maguire et al.
The Journal of pharmacology and experimental therapeutics, 345(3), 354-362 (2013-03-29)
Cannabinoid receptor agonists enhance the antinociceptive effects of μ-opioid receptor agonists, which suggests that combinations of these drugs might enhance therapeutic effectiveness (e.g., analgesia). However, it is not clear whether combinations of these drugs also enhance abuse or dependence liability.
Suspected dronabinol withdrawal in an elderly cannabis-naive medically ill patient.
Russ S Muramatsu et al.
The American journal of psychiatry, 170(7), 804-804 (2013-07-04)
M Waldman et al.
Biochemical pharmacology, 85(11), 1626-1633 (2013-03-30)
Tetrahydrocannabinol (THC), the major psychoactive component of marijuana, is a cannabinoid agonist that exerts its effects by activating at least two specific receptors (CB1 and CB2) that belong to the seven transmembrane G-protein coupled receptor (GPCR) family. Both CB1 and
Erik T Garbacik et al.
Journal of biomedical optics, 18(4), 046009-046009 (2013-04-17)
Nature has developed many pathways to produce medicinal products of extraordinary potency and specificity with significantly higher efficiencies than current synthetic methods can achieve. Identification of these mechanisms and their precise locations within plants could substantially increase the yield of
S Ameur et al.
Analytical and bioanalytical chemistry, 405(10), 3117-3123 (2013-01-29)
A cloud point extraction coupled with high performance liquid chromatography (HPLC/UV) method was developed for the determination of Δ(9)-tetrahydrocannabinol (THC) in micellar phase. The nonionic surfactant "Dowfax 20B102" was used to extract and pre-concentrate THC from cannabis resin, prior to
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