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S(-)-CATHINONE HYDROCHLORIDE

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S(-)-CATHINONE HYDROCHLORIDE Basic information

Product Name:
S(-)-CATHINONE HYDROCHLORIDE
Synonyms:
  • S(-)-Cathinone HCl
  • S(-)-2-AMINO-1-PHENYL-1-PROPANONE HYDROCHLORIDE
  • S(-)-CATHINONE HYDROCHLORIDE
  • Methanol（Test S(-)-Cathinone HCl, 1.0 mg/mL as free base）
  • S(-)-Cathinone hydrochloride solution
  • ()-(S)-Cathinone (hydrochloride) (exempt preparation)
  • (2S)-2-amino-1-phenylpropan-1-one:hydrochloride
  • (?)-(S)-Cathinone hydrochloride
CAS:
72739-14-1
MF:
C9H12ClNO
MW:
185.65
EINECS:
804-103-9
Mol File:
72739-14-1.mol
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S(-)-CATHINONE HYDROCHLORIDE Chemical Properties

Flash point:
9℃
storage temp. 
-20°C
solubility 
DMF: 30 mg/ml
DMSO: 30 mg/ml
Ethanol: 30 mg/mlPBS (pH 7.2): 10 mg/ml
form 
liquid
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Safety Information

Hazard Codes 
F,T
Risk Statements 
11-23/24/25-39/23/24/25
Safety Statements 
7-16-36/37-45
RIDADR 
UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany 
1
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S(-)-CATHINONE HYDROCHLORIDE Usage And Synthesis

Chemical Properties

White Solid

Uses

Psychoactive alkaloid found in the leaves of the khat plant, Catha edulis Forsk., Celastraceae. Controlled substance (stimulant).

General Description

This Certified Spiking Solution? is suitable for GC/MS or LC/MS testing applications involving cathinone in clinical toxicology, forensic analysis or urine drug testing. Cathinone, or benzoylethanamine, is a major active constituent of the recreational drug “Khat”. This stimulant has also been found in illicit bath salts.

References

[1] TERRY A DAL CASON  Richard A G  Richard Young. Cathinone: An Investigation of Several N-Alkyl and Methylenedioxy-Substituted Analogs[J]. Pharmacology Biochemistry and Behavior, 1997, 58 4: Pages 1109-1116. DOI: 10.1016/s0091-3057(97)00323-7
[2] PETER KALIX  Richard A G. Further evidence for an amphetamine-like mechanism of action of the alkaloid cathinone[J]. Biochemical pharmacology, 1986, 35 18: Pages 3015-3019. DOI: 10.1016/0006-2952(86)90380-1
[3] RICHARD A. GLENNON  Stephen M L. Serotonin receptor affinity of cathinone and related analogs[J]. Journal of Medicinal Chemistry, 1982, 25 4: 393-397. DOI: 10.1021/jm00346a012

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