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Buphedrone metabolite (hydrochloride) ((±)-Ephedrine stereochemistry)

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    Buphedrone metabolite (hydro<wbr>chloride) ((±)-<wbr/>Ephedrine stereo<wbr/>chemistry)
  • Buphedrone metabolite (hydro<wbr>chloride) ((±)-<wbr/>Ephedrine stereo<wbr/>chemistry)
Cat No: 9001432
Biochemicals - Analytical Standards
Cayman

Buphedrone is a substituted cathinone characterized by an ethyl group at the α position and an N-terminal methyl group. This metabolite of buphedrone features conversion of the β-keto group to β-hydroxy and is an enantiomeric mixture of the R,S and S,...

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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:
  • (?S)-rel-[(1R)-1-(methylamino)propyl]-benzenemethanol, monohydrochloride
Correlated keywords:
  • 63199-79-1 cathinones forensics neurosciences buphedrones metabolites ephedrines stereochemistry keto hydroxyl beta b .beta. R S ethyls groups N-terminal terminals N alpha .alpha. ? positions methyls hydrochlorides ephedrines stereochemistry conversions orientations research analytical references standards HCl ?-keto b-keto beta-keto .beta.-keto ?-hydroxy b-hydroxy beta-hydroxy .beta.-hydroxy R,S
Product Overview:
Buphedrone is a substituted cathinone characterized by an ethyl group at the α position and an N-terminal methyl group. This metabolite of buphedrone 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 evaluated. This product is intended for forensic and research purposes.
Size 1 mg
Shipping dry ice
CAS Number 63199-70-2
Molecular Formula C11H17NO • HCl
SMILES CN[C@@H](CC)[C@H](O)C1=CC=CC=C1.Cl
Molecular Weight 215,7
Formulation A crystalline solid
Purity ≥98%
Custom Code 3822.19
UNSPSC code 12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

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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ISO Guide 34:2009

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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