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560529

Sigma-Aldrich

3,4-Methylenedioxyphenethylamine hydrochloride

98%

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About This Item

Formula empirica (notazione di Hill):
C9H11NO2 · HCl
Numero CAS:
1653-64-1
Peso molecolare:
201.65
Numero MDL:
MFCD00035193
Codice UNSPSC:
12352100
ID PubChem:
24879873
NACRES:
NA.22

Livello qualitativo

100

Saggio

98%

Punto di fusione

216-218 °C (lit.)

Gruppo funzionale

amine

Stringa SMILE

Cl.NCCc1ccc2OCOc2c1

InChI

1S/C9H11NO2.ClH/c10-4-3-7-1-2-8-9(5-7)12-6-11-8;/h1-2,5H,3-4,6,10H2;1H
NDYXFQODWGEGNU-UHFFFAOYSA-N

Descrizione generale

3,4-Methylenedioxyphenethylamine hydrochloride can be synthesized by reacting aluminum chloride, LiAlH4 and 3,4-methylenedioxyphenylacetonitrile.

Applicazioni

3,4-Methylenedioxyphenethylamine hydrochloride may be used to synthesize N-(3,4-methylenedioxyphenethyl)-2-(3-bromo-4-methoxyphenyl)acetamide.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
MKCN9224
MKCN0435
MKCJ4899
MKCJ1648
MKCF7274

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Sigma-Aldrich

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Phenethylamine 99%

Sigma-Aldrich

128945

Phenethylamine

Kjell A Mortier et al.
Rapid communications in mass spectrometry : RCM, 16(9), 865-870 (2002-04-12)
Paramethoxyamphetamine (PMA) is an amphetamine-like designer drug that has emerged recently on the European illicit drug market. This drug has a wicked reputation, as a number of lethal intoxications have occurred. A method using high-performance liquid chromatography coupled to ion
Laura Aalberg et al.
Journal of chromatographic science, 41(5), 227-233 (2003-07-05)
Three regioisomeric 3,4-methylenedioxyphenethylamines having the same molecular weight and major mass spectral fragments of equivalent mass have been reported as components of clandestine drug samples in recent years. These drugs of abuse are 3,4-methylenedioxy-N-ethylamphetamine, 3,4-methylenedioxy-N,N-dimethylamphetamine, and N-methyl-1-(3,4-methylenedioxyphenyl)-2-butanamine. These three compounds
Jan G Bruhn et al.
Journal of psychoactive drugs, 40(2), 219-222 (2008-08-30)
Human interest in psychoactive phenethylamines is known from the use of mescaline-containing cacti and designer drugs such as Ecstasy. From the alkaloid composition of cacti we hypothesized that substances resembling Ecstasy might occur naturally. In this article we show that
An aryne route to laureline, and related topics.
Gibson MS, et al.
J. Chem. Soc. Sect. C, 16, 2234-2238 (1970)
Jon E Sprague et al.
The Journal of pharmacology and experimental therapeutics, 305(1), 159-166 (2003-03-22)
An acute and potentially life-threatening complication associated with the recreational use of the 3,4-methylenedioxymethamphetamine (MDMA, Ecstasy) is hyperthermia. In the present study, Sprague-Dawley rats treated with MDMA (40 mg/kg s.c.) responded with a significant increase (maximal at 1 h) in
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