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1-(4-methoxyphenyl)-N,N-dimethylpropan-2-amine, commonly referred to as 4-MDMPA, is a chemical compound characterized by its stimulant and psychoactive properties. It is a member of the substituted amphetamine class and bears a structural resemblance to the well-known recreational drug MDMA. 4-MDMPA is recognized for its ability to induce heightened alertness, euphoria, and a sense of empathy and sociability in users. Despite its reported recreational use, often in combination with other substances, the compound's pharmacology, toxicology, and long-term effects remain largely unknown. Consequently, 4-MDMPA is not sanctioned for any medical or research applications and is classified as a novel psychoactive substance, which may entail considerable health and safety risks.

26070-48-4

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26070-48-4 Usage

Uses

Used in Recreational Drug Use:
1-(4-methoxyphenyl)-N,N-dimethylpropan-2-amine is used as a psychoactive substance for its ability to produce stimulant effects, including increased alertness, euphoria, and enhanced sociability. However, due to the lack of research and regulatory approval, its use in this context is associated with significant health risks and is not recommended.

Check Digit Verification of cas no

The CAS Registry Mumber 26070-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,7 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 26070-48:
(7*2)+(6*6)+(5*0)+(4*7)+(3*0)+(2*4)+(1*8)=94
94 % 10 = 4
So 26070-48-4 is a valid CAS Registry Number.

26070-48-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methoxyphenyl)-N,N-dimethylpropan-2-amine

1.2 Other means of identification

Product number -
Other names 4-methoxy-N,N-dimethylamphetamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:26070-48-4 SDS

26070-48-4Relevant academic research and scientific papers

Chemical Behavior of N-Alkyl-N-methylbenzylammonium N-Alkylide

Okazaki, Seiji,Shirai, Naohiro,Sato, Yoshiro

, p. 334 - 337 (2007/10/02)

N-Alkyl-N-methyl(4-substituted benzyl)ammonium N-alkylides (3), produced by fluoride ion induced desilylation of N-alkyl-N-methyl-N-(4-substituted benzyl)-1-(trimethylsilyl)alkylammonium iodides (2), were mainly converted into N-alkyl-N-methyl-1-(4-substituted benzyl)alkylamines (5, Stevens rearrangement products) and 4-substituted toluenes (8).Both compounds were produced via radical-forming and -destroying pathways from 2-substituted-6--5-methylene-1,3-cylohexadienes (4), which were initially formed from 3 by sigmatropic rearrangement.There is no direct migration pathway from 3 to 5.

POTENTIAL ANTIDEPRESSANTS: 1-(4-(AMINOALKOXY)PHENYL)-2-PROPYLAMINES

Kmonicek, Vojtech,Vejdelek, Zdenek,Holubek, Jiri,Valchar, Martin,Protiva, Miroslav

, p. 1721 - 1733 (2007/10/02)

1-(4-Hydroxyphenyl)-2-propylamine (X) and its N-monomethyl (XI) and N,N-dimethyl (XII) derivatives were O-alkylated with six tert.aminoalkyl chlorides to aminoalkyl ethers Ia-VIc.In cases of X and XI the reactions were complicated by O,N-dialkylation leading to isolation of triamino ethers XVI and XVII. 1-(4-Hydroxyphenyl)propan-2-one was alkylated with 2-dimethylaminoethyl chloride and the ether XIII was obtained.An attempt to transform 4-(2-dimethylaminoethoxy)benzaldehyde to the 1-aryl-2-nitropropene XIV by heating with nitroethane in acetic acid in the presence of ammonium acetate resulted in the formation of 4-(2-dimethylaminoethoxy)benzonitrile (XV).In the form of salts the amino ethers prepared were tested for antidepressant activity but proved little active or inactive.

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