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M-015

Supelco

Methaqualone solution

1 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®

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About This Item

Empirical Formula (Hill Notation):
C16H14N2O
CAS Number:
Molecular Weight:
250.30
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

certified reference material

form

liquid

packaging

ampule of 1 mL

manufacturer/tradename

Cerilliant®

drug control

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

concentration

1 mg/mL in methanol

technique(s)

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

application(s)

clinical testing

format

single component solution

storage temp.

2-8°C

SMILES string

Cc1ccccc1N2C(C)=Nc3ccccc3C2=O

InChI

1S/C16H14N2O/c1-11-7-3-6-10-15(11)18-12(2)17-14-9-5-4-8-13(14)16(18)19/h3-10H,1-2H3

InChI key

JEYCTXHKTXCGPB-UHFFFAOYSA-N

General description

Methaqualone is a sedative-hypnotic and a central nervous system depressant sold under the trade name Quaalude for treatment of insomnia. Methaqualone also has a history of abuse, known by street names such as Disco biscuits, Lemmons, and 714s. This certified solution standard is applicable for use as starting material in calibrators or controls for a variety of LC/MS or GC/MS applications from urine drug testing to forensic analysis and clinical toxicology.

Application


  • Pharmacokinetic studies: The analysis of Methaqualone in pharmacokinetic research employs liquid chromatography/tandem mass spectrometry, crucial for understanding its metabolism and excretion patterns. Such studies are vital for developing safety profiles and therapeutic guidelines for sedative-hypnotics (Yun et al., 2007).

Legal Information

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Target Organs

Eyes

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

49.5 °F - closed cup

Flash Point(C)

9.7 °C - closed cup


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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G McCarthy et al.
The Cochrane database of systematic reviews, (2)(2), CD004146-CD004146 (2005-04-23)
Methaqualone is a potent quinazoline, a class of sedative-hypnotics, that has a high potential for abuse. While the oral use of methaqualone (Quaalude, Mandrax) has waned in western countries since the mid-late 1980's, the practice of smoking methaqualone is a
N Fucci
The American journal of forensic medicine and pathology, 17(3), 231-232 (1996-09-01)
A case of acute intoxication of both methaqualone and diphenhydramine is reported. The analysis of these compounds was performed by liquid-liquid extraction (Toxi-Lab DPC procedure) followed by gas chromatography/mass spectrometry determination; both substances are contained in the pharmaceutical formulation called
Arvin Bhana et al.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 92(7), 542-547 (2002-08-29)
To provide community-level public health surveillance information on cannabis and Mandrax (methaqualone) use and associated health and social consequences. A descriptive, epidemiological study of cannabis and Mandrax supply and demand indicators based on data gathered from multiple sources, including specialist
Charles D H Parry et al.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 95(6), 429-432 (2005-08-17)
To assess the extent of cannabis and other drug use among patients presenting with recent injuries at trauma units in Cape Town, Port Elizabeth and Durban from 1999 to 2001. Cross-sectional surveys were conducted during a 4-week period at each
A Ceschi et al.
Clinical toxicology (Philadelphia, Pa.), 51(1), 54-57 (2013-01-10)
Methylmethaqualone is a sedative designer drug created by adding a methyl group to the 3-phenyl ring of methaqualone, and is at present not subject to restrictive regulation in many countries. To our knowledge, no case of methylmethaqualone abuse has been

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