4-Methyl<wbr/>ethcathinone metabolite (hydro<wbr>chloride) ((±)-<wbr/>Pseudo<wbr/>ephedrine stereo<wbr/>chemistry)

4-Methylethcathinone metabolite (hydrochloride) ((±)-Pseudoephedrine stereochemistry)

CAT N°: 9001436

4-methylethcathinone (4-MEC) (hydrochloride) (Item No. 9001069) is a cathinone derivative identified in several designer, recreational drugs that are sold as “legal high” replacements for controlled stimulants such as methamphetamine and 3,4-methylenedioxymethamphetamine.{19500,19914,19498} This metabolite of 4-MEC features conversion of the ?-keto group to ?-hydroxy and is an enantiomeric mixture of the R,R and S,S orientations at carbons one and two, as in pseudoephedrine. The physiological and toxicological properties of this compound have not been elucidated. This product is intended for research and forensic applications.

Territorial Availability: Available through Bertin Technologies only in France

Technical Warning: Bertin Technologies restricts the sale of this product to licensed controlled substance laboratories and qualified academic research institutions. Please contact us for further details.

Special Advice: Please check regulation status before ordering; additionel fees can apply.

  • Synonyms
    • (1R,2R)-2-(ethylamino)-1-(p-tolyl)propan-1-ol, monohydrochloride
  • Correlated keywords
    • forensics sciences designer drugs methamphetamines 4methylethcathinone 4 methylethcathinones mephedrones cathinones analogs MDMA amphetamines plants feeders pseudoephedrines stereochemistry analytical references standards four-methylethcathinones four neuroscience
  • Product Overview:
    4-methylethcathinone (4-MEC) (hydrochloride) (Item No. 9001069) is a cathinone derivative identified in several designer, recreational drugs that are sold as “legal high” replacements for controlled stimulants such as methamphetamine and 3,4-methylenedioxymethamphetamine.{19500,19914,19498} This metabolite of 4-MEC features conversion of the ?-keto group to ?-hydroxy and is an enantiomeric mixture of the R,R and S,S orientations at carbons one and two, as in pseudoephedrine. The physiological and toxicological properties of this compound have not been elucidated. This product is intended for research and forensic applications.

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