CAS 486459-03-4
:4-Bromomethcathinone
Description:
4-Bromomethcathinone, also known as 4-BMC, is a synthetic cathinone that belongs to a class of compounds known as substituted phenethylamines. It is structurally related to methcathinone, with a bromine atom substituted at the para position of the phenyl ring. This compound is typically encountered as a white crystalline powder and is known for its stimulant properties, which can include increased energy, euphoria, and enhanced sociability. The mechanism of action is thought to involve the inhibition of the reuptake of neurotransmitters such as dopamine, norepinephrine, and serotonin, leading to increased levels of these chemicals in the brain. However, the safety profile and long-term effects of 4-Bromomethcathinone are not well-studied, and its use can be associated with various adverse effects, including cardiovascular issues, anxiety, and potential for addiction. Due to its psychoactive properties, it is often subject to legal restrictions in many jurisdictions. As with any research chemical, caution is advised regarding its use and potential health risks.
Formula:C10H12BrNO
InChI:InChI=1S/C10H12BrNO/c1-7(12-2)10(13)8-3-5-9(11)6-4-8/h3-7,12H,1-2H3
InChI key:InChIKey=OOJXMFNDUXHDOV-UHFFFAOYSA-N
SMILES:C(C(NC)C)(=O)C1=CC=C(Br)C=C1
Synonyms:- 1-Propanone, 1-(4-bromophenyl)-2-(methylamino)-
- 4-Bromomethcathinone
- 1-(4-Bromophenyl)-2-(methylamino)-1-propanone
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100
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50
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90
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95
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100
Found 2 products.
4-Bromomethcathinone-D3 Hydrochloride
CAS:Controlled Product<p>Applications 4-Bromomethcathinone-D3 hydrochloride is a labelled analogue of 4-Bromomethcathinone hydrochloride (B686080). 4-Bromomethcathinone is part of a family of synthetic cathinone compounds called aminopropiophenones (which have high potential for abuse). Aminopropiophenones have potential psychoactive effects, can lead to death, and are labelled as highly controlled substances in many countries.<br>References Foley, K. & Cozzi, N.: Drug Dev. Res., 60, 252 (2003); Mas-Morey, P., et al.: J. Pharm. Pract., 26, 353 (2013); Penders, T., et al.: Gen. Hosp. Psych., 34, 647 (2012); Spiller, H., et al.: Clin. Toxicol., 49, 499 (2011)<br></p>Formula:C10D3H9BrNO·HClColor and Shape:NeatMolecular weight:281.592Dimethylphenidate
CAS:Controlled Product<p>Dimethylphenidate is a psychostimulant drug that stimulates the central nervous system. It is a prodrug that is metabolized in the body to produce two active metabolites, amphetamine and methamphetamine. Dimethylphenidate binds to histamine H1 receptors and modulates the release of neurotransmitters such as dopamine and serotonin. The drug has been shown to have low uptake in rat brain tissue, which may be due to its ability to bind with high affinity to the serotonin transporter. This binding prevents uptake of serotonin from the synaptic cleft into presynaptic neurons by blocking membrane transporters responsible for transporting serotonin back into the neuron. Dimethylphenidate can also block dopamine reuptake by inhibiting dopamine transporter activity on dopamine-containing neurons in the brain, thereby increasing levels of extracellular dopamine.</p>Formula:C10H12BrNOPurity:Min. 95%Molecular weight:242.11 g/mol

