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CAS NO:: | 404950-80-7 | Purity:: | ≥98% |
---|---|---|---|
Molecular Formula:: | C21H23N3O2 | Molecular Weight:: | 349.42622 |
Name: Medhylone: | Medhylone Bk Mdma Methylone | Email:: | Aimee@hiersunchem.com |
Skype:: | Aimeechem-168 | ||
High Light: | Pharmaceutical Ingredients,Chemical Intermediates |
Name: medhylone
CAS NO:404950-80-7
Purity:≥99.5%
Appearance: crystal
Molecular formula:C21H23N3O2
Molecular weight: 349.42622
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5-Methylethylone
Material:Research Chemical
Properties:White powder
Application:For lab research only
Systematic IUPAC name: 2-(Ethylamino)-1-(7-methyl-1,3-benzodioxol-5-yl)-1-propanone
Other names: R-MMC; 3,4-Methylenedioxy-5-methyl-N-ethyl ; 5-Methyl-βk-MDEA
CAS Registry Number: 1364933-82-3
Chemical formula: C13H17NO3
Molar mass: 235.28 g·mol−1
Appearance: white powder
Purity: above 99%
Package: aluminium foil bag or according requirement
MED/5-Methylethylone is similiar to 5-Methyl-MDA, Butylone, Methylone.
If have need, contact us freely.
Methylone (also known as "3,4-methylenedioxy-N-methylcathinone", "MDMC", "βk-MDMA" and by the slang term "M1") is anempathogen and stimulant psychoactive drug. It is a member of the substituted amphetamine, substituted cathinone and substituted methylenedioxyphenethylamine classes.
Methylone is the substituted cathinone analog of MDMA and the 3,4-methylenedioxy analog of methcathinone. The only structural difference of methylone with respect to MDMA is the substitution of 2 hydrogen atoms by 1 oxygen atom in the β position of thephenethylamine core, forming a ketone group.[2]
Methylone was first synthesized by the chemists Peyton Jacob III and Alexander Shulgin in 1996 for potential use as an antidepressant.[3] Starting around 2004, methylone has been sold for recreational use, taking advantage of the absence of legal prohibition of this compound in many countries.
In spite of these behavioral and pharmacological similarities between methylone and MDMA, the observed subjective effects of both drugs are not completely identical. Alexander Shulgin wrote of the former:
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