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1246816-62-5

1246816-62-5 Structure

1246816-62-5 Structure
IdentificationBack Directory
[Name]

3-Methyl Methcathinone Hydrochloride
[CAS]

1246816-62-5
[Synonyms]

3-MMC
3-Methylmethcathinone
3-Methylmethcathinone, 3-MMC
3-Methyl Methcathinone Hydrochloride
3-Methyl Methcathinone Hydrochloride,3MMC
3-Methylmethcathinone (hydrochloride) (exempt preparation)
2-(methylamino)-1-(3-methylphenyl)propan-1-one:hydrochloride
2-(MethylaMino)-1-(3-Methylphenyl)-1-propanone, Monohydrochloride
[Molecular Formula]

C11H16ClNO
[MOL File]

1246816-62-5.mol
[Molecular Weight]

213.71
Chemical PropertiesBack Directory
[Melting point ]

193-195°C
[storage temp. ]

Controlled Substance, -20°C Freezer
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

White to Off-White
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H336-H335
[Precautionary statements ]

P261-P271-P304+P340-P312-P403+P233-P405-P501
Hazard InformationBack Directory
[Description]

4-Methylmethcathinone (4-methyl MC) is a psychoactive synthetic cathinone that has been identified in bath salts and powders. 3-Methylmethcathinone (3-methyl MC) (hydrochloride) is a potential major impurity in preparations of 4-methyl MC. As an isomer of 4-methyl MC, it is likely to have psychoactive properties and may itself be marketed as a designer drug. The physiological and toxicological properties of this compound have not been determined. This product is intended for forensic and research applications.
[Chemical Properties]

Off-White Solid
[Uses]

Methcathinone derivative.
[References]

[1] MATILDA B?CKBERG. Characteristics of analytically confirmed 3-MMC-related intoxications from the Swedish STRIDA project.[J]. Clinical Toxicology, 2015, 53 1: 46-53. DOI: 10.3109/15563650.2014.981823
[2] HUI ZHI SHIRLEY LEE. Identification of closely related new psychoactive substances (NPS) using solid deposition gas-chromatography infra-red detection (GC–IRD) spectroscopy[J]. Forensic science international, 2019, 299: Pages 21-33. DOI: 10.1016/j.forsciint.2019.03.025
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