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2-Amino-1-phenylbutane (hydrochloride)

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    2-<wbr/>Amino-<wbr/>1-<wbr/>phenylbutane (hydro<wbr>chloride)
  • 2-<wbr/>Amino-<wbr/>1-<wbr/>phenylbutane (hydro<wbr>chloride)
Cat No: 9001864
Biochemicals - Analytical Standards
Cayman

Amphetamines are chemical compounds characterized by an α-methylphenethylamine base structure. D-amphetamine (Item No. 14204) is a stimulant that binds the norepinephrine and dopamine transporters (EC50s = 7.1 and 24.8 nM, respectively).{23316} 2-Amino...

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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:
  • ?-ethyl-benzeneethanamine, monohydrochloride
Correlated keywords:
  • 30543-88-5 53309-?89-?0 84524-?40-?3 amphetamines forensics neurosciences analytical references standards ethyl alpha mixes mixtures D L isomers aminos phenylbutane HCl phenethylamines Phenylisobutylamine Phenyl-sec-butylamine sciences designers drugs dietary supplements metabolites psychoactive recreational stimulants craze 20735-15-3 DEPEA 1-phenyl-2-butanamine substituted
Product Overview:
Amphetamines are chemical compounds characterized by an α-methylphenethylamine base structure. D-amphetamine (Item No. 14204) is a stimulant that binds the norepinephrine and dopamine transporters (EC50s = 7.1 and 24.8 nM, respectively).{23316} 2-Amino-1-phenylbutane is an amphetamine characterized by having an ethyl group in the alpha position. It has emerged as a potential recreational drug.{24764,24766} This product is a mixture of the D and L isomers. The D isomer of this compound partially substitutes for D-amphetamine in an animal discrimination analysis, suggesting that it weakly mimicks the signaling and stimulant properties of D-amphetamine.{24765} This product is intended for forensic and research applications.
Size 1 mg
Shipping dry ice
CAS Number 20735-15-3
Molecular Formula C10H15N • HCl
SMILES NC(CC)CC1=CC=CC=C1.Cl
Molecular Weight 185,7
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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