26070-48-4

Basic information

• Product Name: 1-(4-methoxyphenyl)-N,N-dimethylpropan-2-amine
• CAS NO: 26070-48-4
• Molecular Formula: C₁₂H₁₉NO
• Molecular Weight: 193.2854
• Mol File: 26070-48-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 267.4°C at 760 mmHg
• Flash Point: 78.5°C
• Density: 0.95g/cm³
• Vapor Pressure: 0.00815mmHg at 25°C
• Refractive Index: 1.502
• CAS DataBase Reference: 1-(4-methoxyphenyl)-N,N-dimethylpropan-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methoxyphenyl)-N,N-dimethylpropan-2-amine(26070-48-4)
• EPA Substance Registry System: 1-(4-methoxyphenyl)-N,N-dimethylpropan-2-amine(26070-48-4)

Safety Data

• Hazardous Substances Data: 26070-48-4(Hazardous Substances Data)

Usage

General Description

1-(4-methoxyphenyl)-N,N-dimethylpropan-2-amine, also known as 4-MDMPA, is a chemical compound with stimulant and psychoactive properties. It belongs to the class of substituted amphetamines and is structurally similar to the recreational drug MDMA. 4-MDMPA is known to produce effects such as increased alertness, euphoria, and feelings of empathy and sociability. It has been reported to be used as a recreational drug, often in combination with other substances. However, little is known about its pharmacology, toxicology, and long-term effects, and its use is not approved for any medical or research purposes. As such, it is considered a novel psychoactive substance and may pose significant risks to health and safety.

Upstream product

• 50-00-0 formaldehyd 
• 64-13-1 2-amino-1-(4-methyoxyphenyl)propane 
• 123701-39-3 (4-Methoxy-benzyl)-dimethyl-(1-trimethylsilanyl-ethyl)-ammonium; iodide 
• 22331-70-0 p-Methoxymethamphetamine 
• 74-88-4 methyl iodide 

Downstream Products

• 69792-61-6 N,N-dimethyl-1-(4-hydroxyphenyl)-2-propylamine 

Relevant articles and documents

Selection of a Sommelet-Hauser or a Stevens Rearrangement Pathway of N,N-Dimethyl(substituted benzyl)ammonium N-Alkylides

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

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.