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Merck
CN

SML0194

Sigma-Aldrich

3,4-Methylenedioxypyrovalerone hydrochloride

≥98% (HPLC)

别名:

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

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About This Item

经验公式(希尔记法):
C16H21NO3 · HCl
CAS号:
分子量:
311.80
UNSPSC代码:
12352200

方案

≥98% (HPLC)

表单

powder

药品控制

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)

颜色

white to tan

溶解性

H2O: ≥10 mg/mL

储存温度

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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应用

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

生化/生理作用

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.

特点和优势

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.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral - STOT SE 3

靶器官

Central nervous system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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