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|Molecular Weight:||207 G||Purity:||98.5%|
|Type:||Strong Hard Crystal||Use:||Medical Research ; Chemical Research ;|
Pink brown color BKEBDP BK-MDEA MDEC hard crystal chemicasl for medical research CAS 186028-79-5
bkedbp ; ethylone; methylone; bk-mdea, MDEC, dibutylone
|white, brown, pink, red, blue ;|
hot sale color
|brown, pink ;|
1-2 days; 7-10 days to arrive;
other hot products
|4cl-pvp, 4-cec, hexen, 4-mpd, 4f-php, 5f-adb, fub-amb, fub-akb48, 5c-akb48, mmb-chminaca, etc|
bk-EBDP Crystals is at this time classified as a research compound. This means they are not intended for human or animal consumption and should be used in controlled settings for scientific or forensic research studies only.
N-Methyl-1,3-benzodioxolylpentanamine (MBDP; Methyl-K, UWA-091), also known as 3,4-methylenedioxy-α-propyl-N-methylphenethylamine, is a psychoactive drug of the phenethylamine chemical class.
Methylone (also known as "3,4-methylenedioxy-N-methylcathinone", "MDMC", "βk-MDMA" and by the slang term "M1") is an empathogen 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 the phenethylamine core, forming a ketone group.
Methylone was first synthesized by the chemists Peyton Jacob III and Alexander Shulgin in 1996 for potential use as an antidepressant. Starting around 2004, methylone has been sold for recreational use, taking advantage of the absence of legal prohibition of this compound in many countries.
Methylone substitutes for MDM in rats trained to discriminate MDM from saline. Methylone does not substitute for amphetamine or for the hallucinogenic DOM in animals trained to discriminate between these drugs and saline.
Further, also in common with MDM, methylone acts on monoaminergic systems. In vitro, methylone has one third the potency of MDMA at inhibiting platelet serotonin accumulation and about the same in its inhibiting effects on the dopamine and noradrenaline transporters.
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