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4-Chlorocathinone (hydrochloride) Sale

(Synonyms: 2-amino-4'-Chloropropiophenone, 4'-chloro-2-Aminopropiophenone, p-Chlorocathinone, para-Chlorocathinone) 目录号 : GC46629

An Analytical Reference Standard

4-Chlorocathinone (hydrochloride) Chemical Structure

Cas No.:23184-97-6

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1 mg
¥1,113.00
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5 mg
¥3,906.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

4-Chlorocathinone (hydrochloride) is an analytical reference standard categorized as a cathinone.1 4-Chlorocathinone produces partial stimulus generalization to (±)-cathinone in rats. This product is intended for research and forensic applications.

1.Glennon, R.A., Schechter, M.D., and Rosecrans, J.A.Discriminative stimulus properties of S (-)- and R (+)-cathinone, (+)-cathine and several structural modificationsPharmacol. Biochem. Behav.21(1)1-3(1984)

Chemical Properties

Cas No. 23184-97-6 SDF
别名 2-amino-4'-Chloropropiophenone, 4'-chloro-2-Aminopropiophenone, p-Chlorocathinone, para-Chlorocathinone
Canonical SMILES ClC1=CC=C(C(C(C)N)=O)C=C1.Cl
分子式 C9H10ClNO.HCl 分子量 220.1
溶解度 DMF: 1 mg/ml,DMSO: 30 mg/ml,Ethanol: 1 mg/ml,PBS (pH 7.2): 10 mg/ml 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 4.5434 mL 22.7169 mL 45.4339 mL
5 mM 0.9087 mL 4.5434 mL 9.0868 mL
10 mM 0.4543 mL 2.2717 mL 4.5434 mL
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Research Update

Spectroscopic characterization and crystal structures of two cathinone derivatives: N-ethyl-2-amino-1-phenylpropan-1-one (ethcathinone) hydrochloride and N-ethyl-2-amino-1-(4-chlorophenyl)propan-1-one (4-CEC) hydrochloride

Forensic Toxicol 2017;35(1):114-124.PMID:28127410DOI:PMC5214876

Comprehensive chemical characterization for two cathinone derivatives, N-ethyl-2-amino-1-phenylpropan-1-one (ethcathinone) hydrochloride and N-ethyl-2-amino-1-(4-chlorophenyl)-propan-1-one (4-chloroethcathinone, 4-CEC) hydrochloride, in material seized by drug enforcement agencies was performed by nuclear magnetic resonance (NMR) spectroscopy, infrared spectroscopy, gas chromatography-mass spectrometry in positive electron ionization mode, liquid chromatography-mass spectrometry in positive electrospray ionization mode and X-ray crystallography. The examined samples of these two compounds proved to be very pure for ethcathinone and mixed with very small quantities of other substances for 4-CEC by NMR spectroscopy and mass spectrometry. X-ray crystallographic studies confirmed the occurrence of both compounds as racemic mixtures. These spectroscopic and crystallographic data seem very useful for their identification. Especially for 4-CEC, this is the first description on its spectroscopic characterization in a scientific context to our knowledge.