Cathinones for sale

Under the huge variety of research chemicals included in the cathinones group, synthetic analogues of alkaloids with psychoactive properties are concealed, which are initially found in the leaves of the cat bush, which grows in a number of countries in East Africa and the Arabian Peninsula. The leaves of the kata contain a number of alkaloids with a psychoactive effect, the leading role in the list is occupied by cathinone and cathine. Both cathinone and cathine, when ingested, prevent norepinephrine and dopamine reuptake in the synaptic cleft, which ultimately leads to an increase in the concentration of the latter, and as a result—to the stimulating and euphoric effects development. 

Legal status

The legal status of synthetic cathinones does not have a permanent character, from year to year, from country to country, is constantly changing, and judging by the latest trends towards easing. Since 2010, a large area of ​​European Union has been banned from mephedrone. In the US, to date, in many states, due to the many negative cases associated with the use of synthetic cathinones, there is a temporary ban on MDPV and methylone, but it is likely that temporary measures will be replaced by permanent ones. In view of the more pronounced psychoactive effects on the body, it is the cathinones that are object of interest to the greater parts of research chemicals consumers. Kathine has tens of weaker effects on the body, and therefore interest in it is minimal. Currently, on the legal research chemicals market in Europe, we offer our customers more than 5 legal synthetic analogues of cathinone, which have a pronounced psychoactive effect.

Chemical composition

Returning to the cathinones, it should be noted that this research chemical, more often consists a mixture of several synthetic cathinones, less often from one substance. If, as a result of laboratory tests, one substance can be typed, it is more often 3,4-methylenedioxypyrovalerone (MDPV). The cathinone' composition can also include: mephedrone, butylone, pirovalerone, methedrone, methylone, methcathinone. Basically, cathinone is a keto analogue of the cathine, and as such is able to penetrate the blood-brain barrier much more quickly than cathine, hence, more psychoactive. From our laboratory studies it is obvious that only cathinone can be used to prove the use of kata, only it is determined in urine, 1 day after ingestion. The forms of synthetic cathinones production on the legal research chemicals market are very, very diverse, more often it is a white powder or brown color. Also, it can be either capsules or tablets. Routes of synthetic cathinones administrating, do not differ much from the routes of using other surfactants, regardless of the brand under which they are offered for sale. The powder can be taken intranasally, tablets and capsules are more often consumed orally.


Smoking of synthetic cathinones is not very popular among researchers for one simple reason: synthetic cathinones are rapidly destroyed by heating. The consumed dose amount can vary in a very wide range—from several milligrams to one gram, and higher. In this case, the dose directly depends on the route of administration, and the quality of the research chemical. The average size of the cathinone dose is from 5 to 20 mg. With intranasal use, the effect of the cathinone on the body begins at 5, maximum, after 20 minutes. After 15-30 minutes the action of the cathinone reaches its peak, after which the action passes to the plateau phase, and the maximum duration is about 2 hours. After passing through the plateau phase, the effect of cathinone weakens, this period lasts from 30 to 60 minutes. The total duration of all effects, after use, is in the range of 2 to 3.5 hours. According to some data, after oral administration, the substance begins in 15-30 minutes, and can last up to 7 hours in total. As the dose of the cathinone increases, or in the case of multiple receptions, serious psychotic disorders can develop. Due to the small number of scientific studies conducted, it is reliable to say that with the prolonged use of synthetic cathinones, a classic addiction syndrome develops, and a classic abstinent syndrome is formed—it is not possible.

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2,4-Dimethylmethcathinone (2-Methylmephedrone; 2,4-DMMC)
1-(2,4-Dimethylphenyl)-2-(methylamino)propan-1-one; 2-Methylmephedrone; 2,4-Dmmc; 2,4-Dimethylmethcathinone; AKOS022330301; 1-Propanone, 1-(2,4-dimethylphenyl)-2-(methylamino)- Oral, insufflation, intravenous, rectal, smoking 1-(2,4-dimethylphenyl)-2-(methylamino)propan-1-one 1225623-63-1 C12H17NO 191.274 g/mol


4-Fluoro-NiPP (4F-IVP, 4-Fluoro-iPAVP, 4-Fluoro-NPP)
4-fluoro-N-Isopropyl-Pentedrone; 4-fluoro NPP; 1-Pentanone, 1-(4-fluorophenyl)-2-[(1-methylethyl)amino]-, hydrochloride (1:1); UNII:24445F465D; 4-fluoro IPV, 4-Fluoro-NiPP, 4F-IVP, 4-Fluoro-N-Isopropylpentedrone, 4-Fluoro-α-Isopropylamino-Valerophenone, 4-Fluoro-iPAVP 1-(4-Fluorophenyl)-2-(isopropylamino)-1-pentanone hydrochloride (1:1) C14H21ClFNO 273.774 g/mol


1-(2,3-dihydro-1H-inden-5-yl)-2-(methylamino)propan-1-one 82101165 C13H17NO 203.285 g/mol


DL-4662 (legal analogue of pentedrone and α-PVP)
DL-4662; 1-(3,4-Dimethoxyphenyl)-2-(ethylamino)pentan-1-one; DL 4662; J3.314.550K; 3',4'-Dimethoxy-alpha-(ethylamino)valerophenone; 1-Pentanone, 1-(3,4-dimethoxyphenyl)-2-(ethylamino)- Oral, intranasal, vaporization, intravenous, rectal, sublingual 1-(3,4-dimethoxyphenyl)-2-(ethylamino)pentan-1-one 1674389-55-9 C15H23NO3 265.353 g/mol


Ephylone (legal analogue of ethylone)
N-Ethylpentylone, βk-Ethyl-K, βk-EBDP Oral, nasal, intravenous 2-(Ethylamino)-1-phenyl-1-hexanone hydrochloride 18410-62-3 C14H22ClNO 255.784 g/mol


Indapyrophenidone (legal analogue of α-PVP)
1-(2,3-Dihydro-1H-inden-5-yl)-2-phenyl-2-(1-pyrrolidinyl)ethanone, Ethanone, 1-(2,3-dihydro-1H-inden-5-yl)-2-phenyl-2-(1-pyrrolidinyl)-, 1-(2,3-dihydro-1H-inden-5-yl)-2-phenyl-2-(pyrrolidine-1-yl)ethane-1-one Oral, intranasal, vaporization, intravenous, rectal, sublingual 1-(2,3-dihydro-1H-inden-5-yl)-2-phenyl-2-(pyrrolidin-1-yl)-ethanone 129844581 C21H23NO 305.42 g·mol−1


MDPHP (legal analogue of MDPV)
MDPHP; 3,4-Md-alpha-php; 3,4-Mdphp; Methylenedioxypyrrolidinohexiophenone; 3,4-Methylenedioxy-alpha-pyrrolidinohexanophenone; 1-(1,3-benzodioxol-5-yl)-2-(pyrrolidin-1-yl)hexan-1-one Oral, insufflation, intravenous, rectal, vaporization 1-(1,3-benzodioxol-5-yl)-2-pyrrolidin-1-ylhexan-1-one 776994-64-0 C17H23NO3 289.375 g/mol


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