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

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    4-<wbr/>Methylethcathinone metabolite (hydro<wbr>chloride) ((±)-<wbr/>Ephedrine stereo<wbr/>chemistry)
  • 4-<wbr/>Methylethcathinone metabolite (hydro<wbr>chloride) ((±)-<wbr/>Ephedrine stereo<wbr/>chemistry)
Cat No: 14758
Biochemicals - Analytical Standards
Cayman

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-methylene...

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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,2S)-2-(ethylamino)-1-(p-tolyl)propan-1-ol, monohydrochloride
Correlated keywords:
  • forensic sciences designer drugs methamphetamines 4methylethcathinone 4 methylethcathinones mephedrones cathinones analogs MDMA amphetamines plants feeders ephedrine stereochemistry analytical references standards 4-MEC MEC four
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 β-keto group to β-hydroxy and is an enantiomeric mixture of the R,S and S,R orientations at carbons one and two, as in ephedrine. The physiological and toxicological properties of this compound have not been elucidated. This product is intended for research and forensic applications.
Size 5 mg
Shipping dry ice
Molecular Formula C12H19NO • HCl
SMILES CC1=CC=C([C@@H](O)[C@@H](NCC)C)C=C1.Cl
Molecular Weight 229,8
Formulation A crystalline solid
Purity ≥98%
Custom Code 3822.19
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.

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