Eutylone hydrochloride
Catalog Number: BT-1473894
CAS Number: 17764-18-0
Molecular Formula: C13H18ClNO3
Molecular Weight: 271.741
The product is for non-human research only. Not for therapeutic or veterinary use.
Product Introduction
Description
Eutylone hydrochloride is a synthetic cathinone that belongs to the class of substituted amphetamines. It is a designer drug that has gained popularity in recent years due to its psychoactive effects. Eutylone hydrochloride is known by various street names such as bk-EBDP, β-keto-1,3-benzodioxolyl-N-ethylbutanamine, and N-ethylbutylone. It is a potent stimulant that affects the central nervous system and produces feelings of euphoria, increased energy, and alertness. The drug is commonly used as a recreational drug and has been associated with adverse health effects.
Properties
CAS Number
17764-18-0
Product Name
Eutylone hydrochloride
IUPAC Name
1-(1,3-benzodioxol-5-yl)-2-(ethylamino)butan-1-one;hydrochloride
Molecular Formula
C13H18ClNO3
Molecular Weight
271.741
InChI
InChI=1S/C13H17NO3.ClH/c1-3-10(14-4-2)13(15)9-5-6-11-12(7-9)17-8-16-11;/h5-7,10,14H,3-4,8H2,1-2H3;1H
InChI Key
LZTAJXOEHCOKDE-UHFFFAOYSA-N
SMILES
CCC(C(=O)C1=CC2=C(C=C1)OCO2)NCC.Cl
Synonyms
bk-EBDB;β-keto-Ethylbenzodioxolylbutanamine
Method of Synthesis or Extraction
Eutylone hydrochloride is synthesized using various methods, including reductive amination, condensation, and oxidation. The most commonly used method is reductive amination, which involves the reaction of an amine with a ketone or aldehyde in the presence of a reducing agent. The efficiency and yield of the synthesis process depend on the quality of the starting materials, reaction conditions, and purification methods. The environmental and safety considerations of the synthesis process are significant, as the production of synthetic cathinones involves the use of hazardous chemicals and solvents.
Chemical Structure and Biological Activity
Eutylone hydrochloride has a chemical structure that is similar to other synthetic cathinones, such as methylone and ethylone. The drug acts as a potent inhibitor of the reuptake of dopamine, norepinephrine, and serotonin, leading to increased levels of these neurotransmitters in the brain. The biological targets of eutylone hydrochloride include the monoamine transporters, which are responsible for the uptake of neurotransmitters from the synaptic cleft. The drug has a high potency and can produce significant effects at low doses.
Biological Effects
Eutylone hydrochloride has been shown to affect cell function and signal transduction in various ways. The drug can alter the release and uptake of neurotransmitters, leading to changes in synaptic transmission and neuronal activity. The potential therapeutic effects of eutylone hydrochloride are still under investigation, but the drug has been suggested as a potential treatment for depression, anxiety, and other psychiatric disorders. However, the toxic effects of the drug are also a concern, as eutylone hydrochloride has been associated with adverse health effects, including cardiovascular and neurological complications.
Applications
Eutylone hydrochloride has various applications in scientific research, including medical, environmental, and industrial research. In medical research, the drug has been used to study the mechanisms of action of synthetic cathinones and their potential therapeutic effects. Clinical trials have been conducted to investigate the safety and efficacy of eutylone hydrochloride as a treatment for psychiatric disorders. In environmental research, the drug has been used to study the effects of synthetic cathinones on ecosystems and their role in pollution management. In industrial research, eutylone hydrochloride has been used in manufacturing processes to improve product quality and efficiency. Health and safety considerations are essential in all applications of eutylone hydrochloride.
Future Perspectives and Challenges
The use and study of eutylone hydrochloride face several limitations and challenges. The drug's legal status and availability are significant barriers to research, as the drug is classified as a controlled substance in many countries. The lack of standardized methods for the synthesis and analysis of eutylone hydrochloride also poses challenges to research. Possible solutions and improvements include the development of new synthesis methods and analytical techniques. Future trends and prospects in the application of eutylone hydrochloride in scientific research include the investigation of its potential therapeutic effects and the development of safer and more effective synthetic cathinones.
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