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P-051

Supelco

PMMA hydrochloride solution

1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®

Sinónimos:

p-Methoxymethamphetamine hydrochloride

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About This Item

Fórmula empírica (notación de Hill):
C11H18ClNO
Número de CAS:
3398-68-3
Peso molecular:
215.72
Código UNSPSC:
41116107
NACRES:
NA.24
En este momento no podemos mostrarle ni los precios ni la disponibilidad

grado

certified reference material

Nivel de calidad

300

Formulario

liquid

Características

Snap-N-Spike®/Snap-N-Shoot®

envase

ampule of 1 mL

fabricante / nombre comercial

Cerilliant®

drug control

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

concentración

1.0 mg/mL in methanol (as free base)

técnicas

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

aplicaciones

forensics and toxicology

Formato

single component solution

temp. de almacenamiento

−20°C

cadena SMILES

Cl.CNC(C)Cc1ccc(OC)cc1

InChI

1S/C11H17NO.ClH/c1-9(12-2)8-10-4-6-11(13-3)7-5-10;/h4-7,9,12H,8H2,1-3H3;1H

Clave InChI

IQZVXWOBOYTPER-UHFFFAOYSA-N

Descripción general

PMMA, or para-methoxymethamphetamine, is a stimulant and psychedelic drug closely related to the amphetamine PMA. This designer drug is sometimes used as a substitute for the amphetamine MDMA. This Certified Spiking Solution® is suitable for use in LC/MS or GC/MS amphetamine testing methods in clinical toxicology, forensic analysis, or urine drug testing.

Información legal

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
CERTIFIED SPIKING SOLUTION is a registered trademark of Cerilliant Corporation
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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Palabra de señalización

Danger

Clasificaciones de peligro

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

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

49.5 °F - closed cup

Punto de inflamabilidad (°C)

9.7 °C - closed cup

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Tomáš Páleníček et al.
Pharmacology, biochemistry, and behavior, 98(1), 130-139 (2010-12-21)
Despite poisoning with the ecstasy substitute para-methoxymethamphetamine (PMMA) being typically associated with severe hyperthermia and death, behavioral and toxicological data on this drug are missing. Herein we present the behavioral profile of PMMA, its hyperthermic potency and pharmacokinetic profile in
Roland F Staack et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 789(1), 27-41 (2003-05-03)
Studies are described on the metabolism and the toxicological analysis of the new designer drug rac-p-methoxymethamphetamine (PMMA) in rat urine using gas chromatography-mass spectrometry (GC-MS). The identified metabolites indicated that PMMA was extensively metabolized mainly by O-demethylation to pholedrine and
Miroslava Rohanova et al.
Legal medicine (Tokyo, Japan), 11 Suppl 1, S429-S430 (2009-03-06)
para-Methoxymethamphetamine (PMMA) is an abused psychedelic compound with reports of several intoxications and deaths after ingestion. However, its pharmacokinetics based on a controlled study is unknown and only partial information on its biotransformation is available. Our experimental study was designed
Kei Zaitsu et al.
Forensic science international, 177(1), 77-84 (2007-12-25)
A newly synthesized designer drug, para-methoxyethylamphetamine (PMEA) was unexpectedly detected in the postmortem specimens of fatality involving drug intoxication in 2005, Japan. For unequivocal identification, the isomeric discrimination of PMEA and its positional-isomers was performed by GC/MS with the trifluoroacetylation.
Roland F Staack et al.
Drug metabolism and disposition: the biological fate of chemicals, 32(4), 379-381 (2004-03-25)
p-Methoxymethamphetamine (PMMA) is a new designer drug, listed in many countries as a controlled substance. Several fatalities have been attributed to the abuse of this designer drug. Previous in vivo studies using Wistar rats had shown that PMMA was metabolized
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