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Merck

P-050

Supelco

PMA hydrochloride solution

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

Sinónimos:

p-Methoxyamphetamine hydrochloride

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About This Item

Fórmula empírica (notación de Hill):
C10H16ClNO
Número de CAS:
Peso molecular:
201.69
Número CE:
Código UNSPSC:
41116107
NACRES:
NA.24

grado

certified reference material

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

2-8°C

cadena SMILES

[Cl-].NC(Cc1ccc(cc1)OC)C.[H+]

InChI

1S/C10H15NO.ClH/c1-8(11)7-9-3-5-10(12-2)6-4-9;/h3-6,8H,7,11H2,1-2H3;1H

Clave InChI

VSHZXOLHFRVZND-UHFFFAOYSA-N

Descripción general

PMA, or para-methoxyamphetamine is a ring-substituted phenethylamine with hallucinogenic effects. PMA is known by street names "Dr. Death," "Chicken Powder," and "Chicken Yellow." Toxicity of PMA may occur at doses only slightly above the usual recreation dose.

Información legal

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

Producto relacionado

Referencia del producto
Descripción
Precios

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

Órganos de actuación

Eyes

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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Certificados de análisis (COA)

Lot/Batch Number

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Fatal paramethoxy-amphetamine (PMA) poisoning in the Australian Capital Territory.
Paul G Lamberth et al.
The Medical journal of Australia, 188(7), 426-426 (2008-04-09)
Paul D Callaghan et al.
Journal of neurochemistry, 100(3), 617-627 (2006-12-22)
p-Methoxyamphetamine (PMA) has been implicated in fatalities as a result of 'ecstasy' (MDMA) overdose worldwide. Like MDMA, acute effects are associated with marked changes in serotonergic neurotransmission, but the long-term effects of PMA are poorly understood. The aim of this
M M W Straiko et al.
Neuroscience, 144(1), 223-231 (2006-11-07)
The present study quantified the cleaved form of the microtubule-associated protein tau (cleaved MAP-tau, C-tau), a previously demonstrated marker of CNS toxicity, following the administration of monoamine-depleting regimens of the psychostimulant drugs amphetamine (AMPH), methamphetamine (METH), +/-3,4-methylenedioxymethamphetamine (MDMA), or para-methoxyamphetamine
Diego Bustamante et al.
Pharmacology, biochemistry, and behavior, 79(2), 199-212 (2004-10-27)
The analgesic effects of (+)- and (-)-amphetamine (AMPH), (+/-)-p-methoxyamphetamine (MA), (+/-)-N-methyl-p-methoxyamphetamine (MMA) and (+/-)-N-ethyl-p-methoxyamphetamine (EMA) were compared using two different algesimetric tests in rats. In the formalin test, (+)-AMPH elicited significant antinociception at doses of 0.2, 2 and 8 mg/kg
Amparo Fornés et al.
The Biochemical journal, 412(3), 495-506 (2008-03-18)
The neuronal glycine transporter GLYT2 controls the availability of the neurotransmitter in glycinergic synapses, and the modulation of its function may influence synaptic transmission. The active transporter is located in membrane rafts and reaches the cell surface through intracellular trafficking.

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