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N-Ethylpentylone   - EBK
N-Ethylpentylone   - EBK
N-Ethylpentylone   - EBK
N-Ethylpentylone   - EBK
N-Ethylpentylone   - EBK
N-Ethylpentylone   - EBK
N-Ethylpentylone   - EBK
N-Ethylpentylone   - EBK
  • Stock: In Stock
  • Model: N-Ethylpentylone - EBK
  • Location: Netherlands
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N-Ethylpentylone appears on the black market and on internet forums under different names, including N-ethylnorpentylone, MDEVP, bk-EBDP, bk-ETHYL-K, bk-EPDP, ephylone, and Mercedes. N-Ethylpentylone is available in crystal, powder, rock, capsule, and tablet forms, mostly as a racemate. There have been cases in which N-ethylpentylone was sold as ecstasy/MDMA (tablets marked with the logo characteristic of MDMA) [1]. N-Ethylpentylone, like other synthetic cathinones, can be taken orally, parenterally, and rectally. In addition, based on the information available on internet forums, it can also be taken through intravenous injection, sublingual administration, or nasal insufflation .

User reports indicate that ephylone produces a mixture of classic stimulant and entactogenic effects resembling those of MDMA, methylone and cocaine. Typical effects include stimulation, disinhibition, increased libido, compulsive redosing, and euphoria. Unlike similar substances, however, ephylone is reported to be very long lasting when taken in larger doses. The significance of this is not known, although it may indicate that it has a different toxicity profile compared to other stimulants.


It is strongly discouraged to use this substance in high doses, multiple times in a row, or in combination with other substances 

Previous reports suggest that N-ethylpentylone shows similar activity to other ring-substituted synthetic cathinones of the pyrovalerone type, such as alpha-PVP (1-phenyl-2-(pyrrolidin-1-yl)pentan-1-one) or MDPV (1-(2H-1,3-benzodioxol-5-yl)-2-(pyrrolidin-1-yl)pentan-1-one). N-Ethylpentylone acts as a psychomotor stimulant . According to Costa et al. , N-ethylpentylone inhibited the uptake of the monoamine neurotransmitters norepinephrine, serotonin, and especially dopamine. The researchers also demonstrated that N-ethylpentylone was not a transporter substrate for inducing the release of dopamine, norepinephrine, or serotonin.

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