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(R)-2,5-Dimethoxy-4-methylamphetamine, commonly known as DMMA, is a psychoactive drug belonging to the amphetamine class of compounds. It is a derivative of methamphetamine and shares a similar chemical structure with MDMA (ecstasy). DMMA is recognized for its hallucinogenic and stimulant properties, often used recreationally for its psychedelic effects. This drug can induce alterations in perception, mood, and cognition. However, it is also known for its high potential for abuse and addiction. In the United States, DMMA is classified as a Schedule I controlled substance, making it illegal to manufacture, possess, or distribute without proper authorization. The effects of DMMA on the brain and body are not well-researched, and there is limited information on the potential dangers and risks associated with its use.

43061-13-8

43061-13-8 Suppliers

This product is a nationally controlled contraband or patented product, and the Lookchem platform doesn't provide relevant sales information.

43061-13-8 Usage

Uses

Used in Recreational Settings:
DMMA is used as a recreational drug for its hallucinogenic and stimulant effects, providing users with altered perceptions, mood, and cognition. Its psychedelic properties make it a popular choice among those seeking novel experiences.
Used in Research:
Although limited, DMMA may be utilized as a research chemical to study the effects of psychoactive substances on the brain and their potential applications in medicine. This application is typically restricted to controlled laboratory settings and requires proper authorization due to its Schedule I classification.

Check Digit Verification of cas no

The CAS Registry Mumber 43061-13-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,0,6 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 43061-13:
(7*4)+(6*3)+(5*0)+(4*6)+(3*1)+(2*1)+(1*3)=78
78 % 10 = 8
So 43061-13-8 is a valid CAS Registry Number.

43061-13-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-DOM

1.2 Other means of identification

Product number -
Other names (R)-1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane

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:43061-13-8 SDS

43061-13-8Relevant academic research and scientific papers

Stereospecific synthesis of amphetamines

Wagner, Jared M.,McElhinny Jr., Charles J.,Lewin, Anita H.,Carroll, F. Ivy

, p. 2119 - 2125 (2007/10/03)

Regioselective addition of aryl lithium to commercially available (S)-(+)-propylene oxide provides the corresponding (S)-aryl-2-propanol. The (R)-amphetamine is obtained by conversion of the alcohol to the tosylate followed by azide displacement and hydrogenation. Mitsunobu conversion of the alcohol to the (R)-bromide followed by azide displacement and hydrogenation affords the (S)-amphetamine.

Asymmetric synthesis of phenylisopropylamines

-

, (2008/06/13)

The synthesis of enantiomers of a series of methoxy- and alkyl- substituted phenylisopropylamines is described. The synthesis comprises reducing the imines, formed by the reaction of appropriate phenylacetones with either (+)- or (-)-α-methylbenzylamine, by low-pressure reduction techniques, and subsequently subjecting the optically active N-(α-phenethyl)phenylisopropylamine derivative to hydrogenolysis. The hydrogenolysis products are characterized by enantiomeric purities in the range of 96 - 99%. Yields of products are approximately 60%.