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560529

Sigma-Aldrich

3,4-Methylenedioxyphenethylamine hydrochloride

98%

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1 G
R$ 594,00
5 G
R$ 2.086,00

About This Item

Fórmula empírica (Notação de Hill):
C9H11NO2 · HCl
Número CAS:
Peso molecular:
201.65
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

R$ 594,00


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Ensaio

98%

pf

216-218 °C (lit.)

grupo funcional

amine

cadeia de caracteres SMILES

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

chave InChI

NDYXFQODWGEGNU-UHFFFAOYSA-N

Descrição geral

3,4-Methylenedioxyphenethylamine hydrochloride can be synthesized by reacting aluminum chloride, LiAlH4 and 3,4-methylenedioxyphenylacetonitrile.[1]

Aplicação

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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Substituted amphetamines such as p-chloroamphetamine and the abused drug methylenedioxymethamphetamine cause selective destruction of serotonin axons in rats, by unknown mechanisms. Since some serotonin neurones also express neuronal nitric oxide synthase, which has been implicated in neurotoxicity, the present study
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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

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