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Safety Information

SML0194

Sigma-Aldrich

3,4-Methylenedioxypyrovalerone hydrochloride

≥98% (HPLC)

Synonym(s):

1-(1,3-Benzodioxol-5-yl)-2-(1-pyrrolidinyl)-1-pentanone hydrochloride, MDPV

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About This Item

Empirical Formula (Hill Notation):
C16H21NO3 · HCl
CAS Number:
Molecular Weight:
311.80
UNSPSC Code:
12352200

Assay

≥98% (HPLC)

form

powder

drug control

USDEA Schedule I; Home Office Schedule 1; regulated under CDSA - not available from Sigma-Aldrich Canada; psicótropo (Spain); Decreto Lei 15/93: Tabela IIA (Portugal)

color

white to tan

solubility

H2O: ≥10 mg/mL

storage temp.

2-8°C

InChI

1S/C16H21NO3.ClH/c1-2-5-13(17-8-3-4-9-17)16(18)12-6-7-14-15(10-12)20-11-19-14;/h6-7,10,13H,2-5,8-9,11H2,1H3;1H

InChI key

PYQZNWFQAMFAMT-UHFFFAOYSA-N

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Application

3,4-Methylenedioxypyrovalerone hydrochloride may be used in dopamine-mediated cell signaling studies.

Biochem/physiol Actions

3,4-Methylenedioxypyrovalerone is a derivative of pyrovalerone, a rapidly-absorbed psychostimulant. It belongs to the class of synthetic cathinones often used as performance-enhancing agent by athletes before being banned.
3,4-Methylenedioxypyrovalerone is a norepinephrine-dopamine reuptake inhibitor (NDRI) that acts as a CNS stimulant.
3,4-Methylenedioxypyrovalerone is a norepinephrine-dopamine reuptake inhibitor (NDRI); CNS stimulant.

Features and Benefits

This compound is featured on the Dopamine Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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M Coppola et al.
Toxicology letters, 208(1), 12-15 (2011-10-20)
The illicit marketplace of substances of abuse continually offers for sale legal alternatives to controlled drugs to a large public. In recent years, a new group of designer drugs, the synthetic cathinones, has emerged as a new trend, particularly among
The metabolism of pyrovalerone hydrochloride.
W Michaelis et al.
Journal of medicinal chemistry, 13(3), 497-503 (1970-05-01)

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