Methcathinone chemical structure
Find information on thousands of medical conditions and prescription drugs.

Methcathinone

Methcathinone is an addictive recreational drug that is cheap and simple to synthesize. It is usually snorted, but can be smoked, injected, or taken orally. Methcathinone is currently a DEA Schedule I chemical. more...

Home
Diseases
Medicines
A
B
C
D
E
F
G
H
I
J
K
L
M
Macrodantin
Maprotiline
Marcaine
Marezine
Marijuana
Marinol
Marplan
Matulane
Maxair
Maxalt
Maxolon
MDMA
Measurin
Mebendazole
Mebendazole
Meclofenoxate
Medrol
Mefenamic acid
Mefloquine
Melagatran
Melarsoprol
Meloxicam
Melphalan
Memantine
Metadate
Metamfetamine
Metamizole sodium
Metandienone
Metaxalone
Metenolone
Metformin
Methadone
Methamphetamine
Methaqualone
Metharbital
Methcathinone
Methenamine
Methionine
Methocarbamol
Methohexital
Methotrexate
Methotrexate
Methoxsalen
Methylcellulose
Methyldopa
Methylergometrine
Methylin
Methylphenidate
Methylphenobarbital
Methylprednisolone
Methyltestosterone
Methysergide
Metiamide
Metoclopramide
Metohexal
Metoprolol
Metrogel
Metronidazole
Metyrapone
Mobic
Moclobemide
Modafinil
Modicon
Monopril
Montelukast
Motrin
Moxidectin
Moxifloxacin
Moxonidine
MS Contin
Mucinex
Mucomyst
Mupirocin
Mupirocin
Muse
Mycitracin
Mycostatin
Myfortic
Mykacet
Mykinac
Myleran
Mylotarg
Mysoline
Phentermine
N
O
P
Q
R
S
T
U
V
W
X
Y
Z

History

Methcathinone was first synthesized in Germany in 1928. It was used in the Soviet Union during the 1930s and 1940s as an anti-depressant. Since the 1960s, methcathinone has been used as a recreational drug in the Soviet Union.

Circa 1994, the United States government informed the UN Secretary-General of its opinion that methcathinone should be added to Schedule I of the Convention on Psychotropic Substances.

Chemistry

Methcathinone is very similar in structure to cathinone, a stimulant alkaloid occurring in the shrub Catha edulis (Khat), the synthetic stimulant methamphetamine, and other phenethylamines.

Methcathinone has a single asymmetric carbon atom, thus yielding enantiomeric + and - forms. Chemical Abstract Services registry numbers for the racemic base and hydrochloride forms are 5650-44-2 and 49656-78-2, respectively. The Chemical Abstract Services registry numbers for the base and hydrochloride forms of the S absolute stereochemical configuration are 112117-24-5 and 66514-93-0, respectively.

Various names for methcathinone include:

  • 2-(methylamino)-propiophenone
  • α-methylamino-propiophenone
  • α-N-methyl-aminopropiophenone
  • 2-(methylamino)-1-phenylpropan-1-one
  • N-methylcathinone
  • N-monomethylcathinone
  • Methylcathinone
  • AL-464 (L isomer)
  • AL-422 (racemate)
  • AL-463 (D-isomer)
  • UR1431
  • UR(W)1431

Methcathinone hydrochloride increases spontaneous rodent locomotor activity, potentiates the release of radio-labelled dopamine from dopaminergic nerve terminals in the brain, and causes appetite suppression.

Methcathinone is most commonly made by the oxidation of ephedrine. Oxidation of ephedrine to methcathinone requires almost zero chemistry experience, making it easy to synthesize. Potassium permanganate (KMnO4) is most the commonly used as the oxidant.

Methcathinone can also be synthesized via the oxidation of l-ephedrine using sodium dichromate and sulfuric acid. This process is just as simple as oxidizing the ephedrine with potassium permanganate.

Synthesizing methcathinone from either potassium permanganate or various chromates is considered undesirable because of the low yields. A method that yields more methcathinone is oxidizing ephedrine with sodium hypochlorite.

Methcathinone acts on the body & brain much like methamphetamine & amphetamine do.

Effects

The effects of methcathinone are similar to those of methamphetamine, but generally less intense, and often more euphoric. The effects have been compared to those of cocaine, since it commonly causes hypertension (elevated blood pressure) and tachycardia (elevated heart rate). Reported effects include:

Read more at Wikipedia.org


[List your site here Free!]


Fast Facts: Methcathinone $0.25

Mechanism of Action and Therapeutic Uses of Psychostimulants
ABBREVIATIONS: ADHD = attention-deficit hyperactivity disorder; CNS = central nervous system; MDA = 3,4-methylenedioxyamphetamine; MDMA = 3,4-methylenedioxymethamphetamine; ...
Khat: a potential concern for law enforcement
The word khat (pronounced cot) may not evoke much response from most of American society, but it could herald a significant problem for law enforcement ...
They're synthetic. They're clandestine. They can heal. They can kill - amphetamine-type stimulants
The four challenges posed by the growing use of amphetamine-type stimulants (ATS) in four areas are discussed. These challenges, namely demand, information, ...
Herbal drug sellers could face jail
Suppliers of herbal drugs - sold as an alternative to substances such as ecstasy and cannabis - could face two years in jail as part of a government ...
STATE DIGEST
Superintendent to face trial on theft charges Siren There is sufficient evidence to prosecute the superintendent of the Siren School District on ...
Policy centers on hard-core addicts, treatment
Drug czar Lee P. Brown drops in tonight at Marquette University. Brown, 57, took over the White House Office of National Drug Control Policy in ...

Home Contact Resources Exchange Links ebay