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3-Methyl Methcathinone Hydrochloride, also known as 3-Methylmethcathinone (3-methyl MC), is a psychoactive synthetic cathinone that is often found as a major impurity in preparations of 4-Methylmethcathinone (4-methyl MC). As an isomer of 4-methyl MC, it is likely to have psychoactive properties and may be marketed as a designer drug. However, its physiological and toxicological properties have not been determined. 3-Methyl Methcathinone Hydrochloride is typically an off-white solid and is intended for forensic and research applications.

1246816-62-5

1246816-62-5 Suppliers

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

1246816-62-5 Usage

Uses

Used in Forensic Applications:
3-Methyl Methcathinone Hydrochloride is used as a forensic tool for the identification and analysis of synthetic cathinones in bath salts and powders. Its presence as a major impurity in preparations of 4-methyl MC aids in the detection and differentiation of these substances.
Used in Research Applications:
3-Methyl Methcathinone Hydrochloride serves as a research compound for studying the psychoactive properties and potential risks associated with synthetic cathinones. This helps in understanding the effects of these substances on human health and developing strategies for their regulation and control.

Check Digit Verification of cas no

The CAS Registry Mumber 1246816-62-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,8,1 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1246816-62:
(9*1)+(8*2)+(7*4)+(6*6)+(5*8)+(4*1)+(3*6)+(2*6)+(1*2)=165
165 % 10 = 5
So 1246816-62-5 is a valid CAS Registry Number.

1246816-62-5SDS

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 3-Methylmethcathinone (hydrochloride)

1.2 Other means of identification

Product number -
Other names -

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:1246816-62-5 SDS

1246816-62-5Downstream Products

1246816-62-5Relevant academic research and scientific papers

Systematic Structure-Activity Studies on Selected 2-, 3-, and 4-Monosubstituted Synthetic Methcathinone Analogs as Monoamine Transporter Releasing Agents

Walther, Donna,Shalabi, Abdelrahman R.,Baumann, Michael H.,Glennon, Richard A.

, p. 740 - 745 (2018/11/23)

Methcathinone analogs are appearing on the clandestine market at a rate nearly out-pacing the ability of investigators to examine them on an individual basis. To formulate structure-activity relationship (SAR) generalities, we examined the releasing ability of several simple methcathinone analogs at the three monoamine transporters (i.e., the dopamine, norepinephrine, and serotonin transporters, DAT, NET, and SERT, respectively) using in vitro assay methods. The analogs included methcathinone and 14 other compounds monosubstituted at the 2-, 3-, or 4-position. In general, (a) the 2-substituted analogs were less potent than either the 3- or 4-substituted analogs, (b) the 3- and 4-substituted analogs were relatively similar in potency, (c) methcathinone was the most selective as a DAT-releasing agent, and (d) the 3- and 4-CF3 analogs were the least DAT-selective. For the 15 compounds, there was a significant correlation (r > 0.9) between DAT and NET potency, suggesting relatively similar structure-activity relationships (at least for the compounds examined here). Several of the compounds have appeared on the clandestine market since our studies were initiated, and the present results provide new information on how they might act.