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M3404

Sigma-Aldrich

(±)-p-Methoxyamphetamine hydrochloride

Synonym(s):

PMA hydrochloride

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About This Item

Empirical Formula (Hill Notation):
C10H15NO · HCl
CAS Number:
52740-56-4
Molecular Weight:
201.69
MDL number:
MFCD00051431
UNSPSC Code:
12352200
PubChem Substance ID:
24896840
Pricing and availability is not currently available.

drug control

USDEA Schedule I; Home Office Schedule 1; stupéfiant (France); kontrollierte Droge in Deutschland; regulated under CDSA - not available from Sigma-Aldrich Canada

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
veterinary

SMILES string

Cl.COc1ccc(CC(C)N)cc1

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Biochem/physiol Actions

CNS stimulant and hallucinogen; more potent transport inhibitor and releaser of serotonin than of dopamine.

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301

Precautionary Statements

P301 + P310

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
066K4082
066K4081
075K4113
055K4114
095H4083

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K M Hegadoren et al.
Journal of psychiatry & neuroscience : JPN, 19(1), 57-62 (1994-01-01)
Experiments were conducted to compare the effects of 4-ethoxyamphetamine, a novel "designer" amphetamine, with (+)-amphetamine and an earlier "designer" amphetamine, 4-methoxyamphetamine, on rats. (+)-Amphetamine significantly decreased frequency threshold measures in an intracranial self-stimulation (ICSS) procedure using medial forebrain bundle electrodes
D Wu et al.
Biochemical pharmacology, 53(11), 1605-1612 (1997-06-01)
The interaction of fifteen amphetamine analogs with the genetically polymorphic enzyme CYP2D6 was examined. All fourteen phenylisopropylamines tested were competitive inhibitors of CYP2D6 in human liver microsomes. The presence of a methylenedioxy group in the 3,4-positions of both amphetamine (Ki
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
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.
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)
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