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N-Methyl-1-(3,4-methylenedioxyphenyl)-2-butanamine

  • Cas number：103818-46-8
  • purity：99%
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Product Details

Manufacturer supply top purity N-Methyl-1-(3,4-methylenedioxyphenyl)-2-butanamine 103818-46-8 with GMP standards

  • Molecular Formula: C12H17NO2
  • Molecular Weight: 207.27
  • Vapor Pressure: 0.003mmHg at 25°C 
  • Refractive Index: 1.531 
  • Boiling Point: 284.578 °C at 760 mmHg 
  • Flash Point: 116.566 °C 
  • PSA： 30.49000 
  • Density: 1.079 g/cm3 
  • LogP: 2.34670 

N-Methyl-1-(3,4-methylenedioxyphenyl)-2-butanamine(Cas 103818-46-8) Usage

General Description

N-Methyl-1-(3,4-methylenedioxyphenyl)-2-butanamine, commonly known as MBDB, is a chemical compound that belongs to the amphetamine and phenethylamine classes. It is a psychoactive substance that is structurally similar to the popular recreational drug MDMA, or ecstasy. MBDB is known to produce empathogenic effects, causing feelings of empathy, emotional openness, and increased sociability in users. It is also reported to induce mild stimulant and psychedelic effects. MBDB is a serotonin-norepinephrine-dopamine releasing agent, meaning it increases the levels of these neurotransmitters in the brain, leading to its psychoactive effects. The compound is not approved for medical use and is classified as a controlled substance in many countries due to its potential for abuse and dependence.

InChI:InChI=1/C12H17NO2/c1-3-11(13-2)6-9-4-5-10-8-14-15-12(10)7-9/h4-5,7,11,13H,3,6,8H2,1-2H3

103818-46-8 Relevant articles

Derivatives of 1-(1,3-benzodioxol-5-yl)-2-butanamine: Representatives of a novel therapeutic class

Nichols,Hoffman,Oberlender,Jacob III,Shulgin

, p. 2009 - 2015 (1986)

The α-ethyl phenethylamine derivative 1-...

Stereoselective synthesis of (s)-3,4-methylenedioxyamphetamines from (r)-cyanohydrins

Effenberger, Franz,Jaeger, Juergen

, p. 1370 - 1374 (2007/10/03)

A stereoselective synthesis of (S)-3,4-m...

103818-46-8 Process route

piperonal
120-57-0,30024-74-9

piperonal

MBDB
135795-90-3,103818-46-8

MBDB

Conditions
Conditions Yield
Multi-step reaction with 5 steps
1: diethyl ether / 8 h / Heating
2: 91 percent / KHSO4 / Heating
3: HCOOOH / acetone / 10 h / 40 °C
4: 15percent H2 SO4 / methanol / 2 h / Heating
5: aluminium amalgam, 25percent aq. NaOH / H2 O; propan-2-ol / 2 h
With sodium hydroxide; potassium hydrogensulfate; Peroxyformic acid; aluminium amalgam; sulfuric acid; In methanol; diethyl ether; water; isopropyl alcohol; acetone;
(E)-5-(but-1-en-1-yl)benzo[d][1,3]dioxole
16929-04-7

(E)-5-(but-1-en-1-yl)benzo[d][1,3]dioxole

MBDB
135795-90-3,103818-46-8

MBDB

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1: HCOOOH / acetone / 10 h / 40 °C
2: 15percent H2 SO4 / methanol / 2 h / Heating
3: aluminium amalgam, 25percent aq. NaOH / H2 O; propan-2-ol / 2 h
With sodium hydroxide; Peroxyformic acid; aluminium amalgam; sulfuric acid; In methanol; water; isopropyl alcohol; acetone;

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  • 120-57-0
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    (E)-5-(but-1-en-1-yl)benzo[d][1,3]dioxole

N-Methyl-1-(3,4-methylenedioxyphenyl)-2-butanamine

CAS:103818-46-8

Purity:99%

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