4-methylethcathinone
Structural formula | ||||||||||
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General | ||||||||||
Surname | 4-methylethcathinone | |||||||||
other names |
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Molecular formula | C 12 H 17 NO | |||||||||
Brief description |
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properties | ||||||||||
Molar mass | 191.27 g mol −1 | |||||||||
Physical state |
firmly |
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Melting point |
198–199 ° C (hydrochloride) |
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safety instructions | ||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
4-methylethcathinone or 4-MEC is a psychoactive substance , is within the group of amphetamines to the cathinone - derivatives . When taken by humans, it has a strong stimulating effect , but less entactogenic .
Psychopharmacology and Dosage
4-MEC is a synthetic substance that is chemically similar to methcathinone . The effect includes a feeling of euphoria associated with loss of appetite and increased alertness , sociability and a strong need to talk. 4-methylethcathinone is used as a stimulant by professional drivers and in sports.
After mephedrone was banned in the United Kingdom in April 2010 , a study of 24 legal highs available online found 4-MEC as well as other cathinone derivatives.
Individual evidence
- ↑ a b c Malecki, G .; Nycz, JE; Pazdziorek, T .; Zawiazalec, M .: X-ray structures and computational studies of several cathinones in J. Mol. Struct. 1002 (2011) 10-18, doi : 10.1016 / j.molstruc . 2011.06.030 .
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ↑ a b Thomas Geschwinde: Intoxicating drugs: market forms and modes of action . Springer, 2013, ISBN 978-3-642-30163-6 , pp. 570 ( limited preview in Google Book search).
- ↑ SD Brandt, HR Sumnall, F. Measham, J. Cole: Analyzes of second-generation 'legal highs' in the UK: initial findings. In: Drug Test Anal . 2010; 2: 377-382. doi : 10.1002 / dta.155 .
Web links
- isomerdesign.com: 4-MEC (English)
- 4-methylethcathinone (4-MEC) . In: Erowid . (English)