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ETH-CAT

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ETH-CAT
Chemical Nomenclature
Common names ETH-CAT, Ethcathinone, Ethylpropion
Substitutive name Ethylcathinone
Systematic name (RS)-1-(Benzo[d][1,3]dioxol-5-yl)-N-methylpropan-2-amine
Class Membership
Psychoactive class Stimulant
Chemical class Cathinone
Routes of Administration

WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.



Oral
Dosage
Threshold 60 mg
Light 100 - 150 mg
Common 150 - 225 mg
Strong 225 - 325 mg
Heavy 325 mg +
Duration
Total 3 - 5 hours
Onset 15 - 40 minutes
Come up 15 - 30 minutes
Peak 60 - 90 minutes
Offset 60 - 120 minutes



Insufflated
Dosage
Threshold 5 mg
Light 15 - 35 mg
Common 35 - 70 mg
Strong 70 - 100 mg
Heavy 100 mg +
Duration
Total 2 - 3 hours
Onset 1 - 5 minutes
Come up 15 - 30 minutes
Peak 60 - 90 minutes
Offset 30 - 60 minutes






DISCLAIMER: PW's dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.

Interactions
Summary sheet: ETH-CAT

Ethcathinone (also known as Ethylcathinone, Ethylpropion, and ETH-CAT) is a synthetic stimulant of the cathinone chemical class that produces medium-lived typical amphetamine and cathinone-like stimulation when administered. It is an active metabolite of the prodrug diethylcathinone and is thought to be responsible for its psychoactive effects.

Of the simple substituted cathinones, ethcathinone has been reported to be one of the most moderate and residually enduring in its stimulation. Although it has no strong, habit-forming rush component like mephedrone (4-methylmethcathinone), ethcathinone is often reported to exhibit a tendency to induce compulsive redosing, albeit in a manner to extend the effects rather than reproduce the intial rush. It has a relatively short period of human use but is generally considered to be well tolerated due to the so-called "ceiling effect" it is commonly reported to display with reference to the amount of euphoria it can produce compared to many other cathinone and amphetamine derived stimulants substances.

Historically, ethcathinone has rarely been available on the streets, but was instead primarily distributed as a research chemical on the online grey market.[1][2] However, in 2008 it was identified as an ingredient in both quasi-legal "party pills", and, along with another substituted cathinone, mephedrone, has also been reported as having been sold as "ecstasy"[3]

Due to its short history of human use, moderately compulsive nature, and unknown toxicity profile, it is strongly advised to use harm reduction techniques if choosing to use this substance.

Chemistry

Ethcathinone, or ethylcathinone, is a synthetic alkaloid of the substituted cathinone class. Substituted cathinones derive from [[cathinone[[, the principal active psychoactive component in the khat plant. Cathinone is comprised of a phenethylamine core featuring a phenyl ring bound to an amino (NH2) group through an ethyl chain containing a beta-ketone group. In distinction to its N-methylated lower homolog, methcathinone (M-CAT), ETH-CAT possesses an additional ethyl substitution at Rα. ETH-CAT can be thought of as the cathinone analog of ethylamphetamine given it has the same general formula, differing only in the addition of a single double bonded oxygen.

Cathinone substitutive structure.

Pharmacology

Although the effects of ethcathinone have not been formally studied on the same level as traditional amphetamines or other substituted cathinones like methcathinone, it is possible to speculate that like other simple substituted cathinone, it most likely acts principally as a dopamine and norepinephrine reuptake inhibitor.[4] The result of this is an effective increase in the levels of the norepinephrine and dopamine neurotransmitters in the brain by binding to and partially blocking the transporter proteins that normally clear those monoamines from the synaptic cleft. This allows dopamine and norepinephrine to accumulate within the key area of the brain linked to reward and pleasure to extra-endogenous levels, resulting in stimulating, motivatory and euphoric effects.

Subjective effects

Ethylcathinone at low to moderate doses has been reported as being a relatively functional and effective amphetamine-like stimulant for performing general productivity tasks -- although its short duration of activity combined with its tendency to produce long-lasting residual stimulation may present a drawback compared to other stimulants due to the compulsive redosing it can induce to maintain a steady level of the desired amount of stimulation. However, at higher doses, it becomes less of a productivity-oriented stimulant and more of a recreational one, due to the distracting nature of the euphoria and stimulation it can produce. In this area however, it is reported as falling short of other, more potent related cathinone stimulants such as mephedrone, methylone, and methcathinone.

Disclaimer: The effects listed below cite the Subjective Effect Index (SEI), an open research literature based on anecdotal user reports and the personal analyses of PsychonautWiki contributors. As a result, they should be viewed with a healthy degree of skepticism.

It is also worth noting that these effects will not necessarily occur in a predictable or reliable manner, although higher doses are more liable to induce the full spectrum of effects. Likewise, adverse effects become increasingly likely with higher doses and may include addiction, severe injury, or death ☠.

Physical effects

Cognitive effects

The cognitive effects of ethcathinone can be broken down into several components which intensify proportional to dosage. The general head space of ethcathinone is described by many as one of mental stimulation coupled with mild euphoria, less present than that of amphetamine, even at higher doses.

Visual effects

After effects

The effects which occur during the offset of a stimulant experience generally feel negative and uncomfortable in comparison to the effects which occurred during its peak. This is often referred to as a "comedown" and occurs because of neurotransmitter depletion. Its effects commonly include:

Potentially dangerous interactions

Warning: Many psychoactive substances that are reasonably safe to use on their own can suddenly become dangerous and even life-threatening when combined with certain other substances. The following list provides some known dangerous interactions (although it is not guaranteed to include all of them).

Always conduct independent research (e.g. Google, DuckDuckGo, PubMed) to ensure that a combination of two or more substances is safe to consume. Some of the listed interactions have been sourced from TripSit.

  • "[[DangerousInteraction" contains a listed "[" character as part of the property label and has therefore been classified as invalid.]] - This combination may increase the amount of neurotransmitters such as dopamine to dangerous or even fatal levels. Examples include syrian rue, banisteriopsis caapi, and some antidepressants.[6]
  • Stimulants - Ethylcathinone can be potentially dangerous in combination with other stimulants as it can increase one's heart rate and blood pressure to dangerous levels.
  • "[[DangerousInteraction" contains a listed "[" character as part of the property label and has therefore been classified as invalid.]] & "[[DangerousInteraction" contains a listed "[" character as part of the property label and has therefore been classified as invalid.]] - 25x compounds are highly stimulating and physically straining. Combinations with ETH-CAT should be strictly avoided due to the risk of excessive stimulation and heart strain. This can result in increased blood pressure, vasoconstriction, panic attacks, thought loops, seizures, and heart failure in extreme cases.
  • "[[UncertainInteraction" contains a listed "[" character as part of the property label and has therefore been classified as invalid.]] - Combining alcohol with stimulants can be dangerous due to the risk of accidental over-intoxication. Stimulants mask alcohol's depressant effects, which is what most people use to assess their degree of intoxication. Once the stimulant wears off, the depressant effects will be left unopposed, which can result in blackouts and severe respiratory depression. If mixing, the user should strictly limit themselves to only drinking a certain amount of alcohol per hour.
  • "[[UnsafeInteraction" contains a listed "[" character as part of the property label and has therefore been classified as invalid.]] - Combinations with DXM should be avoided due to its inhibiting effects on serotonin and norepinephrine reuptake. There is an increased risk of panic attacks and hypertensive crisis, or serotonin syndrome with serotonin releasers (MDMA, methylone, mephedrone, etc.). Monitor blood pressure carefully and avoid strenuous physical activity.
  • "[[UnsafeInteraction" contains a listed "[" character as part of the property label and has therefore been classified as invalid.]] - Any neurotoxic effects of MDMA are likely to be increased when other stimulants are present. There is also a risk of excessive blood pressure and heart strain (cardiotoxicity).
  • "[[UncertainInteraction" contains a listed "[" character as part of the property label and has therefore been classified as invalid.]] - Some reports suggest combinations with MXE may dangerously increase blood pressure and increase the risk of mania and psychosis.
  • "[[UncertainInteraction" contains a listed "[" character as part of the property label and has therefore been classified as invalid.]] - Both classes carry a risk of delusions, mania and psychosis, and these risk may be multiplied when combined.
  • "[[UnsafeInteraction" contains a listed "[" character as part of the property label and has therefore been classified as invalid.]] - ETH-CAT may be dangerous to combine with other stimulants like cocaine as they can increase one's heart rate and blood pressure to dangerous levels.
  • "[[DangerousInteraction" contains a listed "[" character as part of the property label and has therefore been classified as invalid.]] - Tramadol is known to lower the seizure threshold[7] and combinations with stimulants may further increase this risk.
  • MDMA - The neurotoxic effects of MDMA may be increased when combined with amphetamines.
  • "[[DangerousInteraction" contains a listed "[" character as part of the property label and has therefore been classified as invalid.]] - This combination may increase the amount of neurotransmitters such as dopamine to dangerous or even fatal levels. Examples include syrian rue, banisteriopsis caapi, and some antidepressants.[8]
  • Cocaine - This combination may increase strain on the heart to dangerous levels.

Toxicity and harm potential

The toxicity and long-term health effects of recreational ethcathinone use do not seem to have been studied in any scientific context and the exact toxic dosage is unknown. This is because ethcathinone has very little history of human usage. Anecdotal reports from people within the community who have tried ethcathinone suggest that there do not seem to be any negative health effects attributed to simply trying this drug at low to moderate doses by itself and using it sparingly (but nothing can be completely guaranteed). Others have commented that its d-isomer form is virtually similar to the effects of d-amphetamine, and thus far little has been shown to give reason to suspect that its toxicity is radically different (though future evidence to the contrary may prove otherwise).

It is strongly recommended that one use harm reduction practices when using this drug.

Tolerance and addiction potential

As with other stimulants, ethcathinone may also possess habit-forming or reinforcing properties. Compared with other stimulants, however chronic use of ethcathinone can be considered only mildly addictive with a comparatively low potential for abuse. Early studies demonstrate ethcathinone suppresses cocaine self-administration in rhesus monkeys, without the adverse effects associated with older DA releasers (e.g., amphetamine).[citation needed] Despite this, ethcathinone may still be capable of causing psychological dependence among certain users.

Tolerance to many of the effects of ethyathinone develops with prolonged and repeated use. This results in users having to administer increasingly large doses to achieve the same effects. After that, it takes about 2 - 3 days for the tolerance to be reduced to half and 5-7 days to be back at baseline (in the absence of further consumption). Ethylcathinone presents cross-tolerance with [[Cross-tolerance::all dopaminergic stimulants]], meaning that after the consumption of ethcathinone all stimulants will have a reduced effect.

Psychosis

Main article: Stimulant psychosis

Abuse of compounds within the amphetamine chemical class at high dosages for prolonged periods of time can potentially result in a stimulant psychosis that may present with a variety of symptoms (e.g., paranoia, hallucinations, or delusions).[9] A review on treatment for amphetamine, dextroamphetamine, and methamphetamine abuse-induced psychosis states that about 5–15% of users fail to recover completely.[10][11] The same review asserts that, based upon at least one trial, antipsychotic medications effectively resolve the symptoms of acute amphetamine psychosis.[12] Psychosis very rarely arises from therapeutic use.[13][14]

Ethylcathinone is currently an unscheduled compound within all parts of the world, meaning its regulation lies in a legal grey area and is not explicitly prohibited within any country. However, people may still be charged for its possession under certain circumstances such as under analogue laws due to its similarity to methcathinone -- a widely prohibited substance -- and with intent to sell or consume.

  • China - As of October 2015 Ethylcathinone is a controlled substance in China.[15]
  • Denmark - Ethcathinone, along with mephedrone and flephedrone, was banned in Denmark on December 18, 2008.[16]
  • United Kingdom - It is illegal to produce, supply, or import this drug under the Psychoactive Substance Act, which came into effect on May 26th, 2016.[17]
  • United States - Ethylcathinone may be considered to be an analog of amphetamine, thus falling under the Federal Analog Act.The Federal Analog Act, 21 U.S.C. § 813, is a section of the United States Controlled Substances Act, allowing any chemical "substantially similar" to an illegal drug (in Schedule I or II) to be treated as if it were also in Schedule I or II, but only if it is intended for human consumption.

See also

References

  1. Isomeric fluoro-methoxy-phenylalkylamines: a new series of controlled-substance analogues (designer drugs) (PubMed.gov / NCBI) | https://www.ncbi.nlm.nih.gov/pubmed/15639609
  2. Chemical analysis of four capsules containing the controlled substance analogues 4-methylmethcathinone, 2-fluoromethamphetamine, alpha-phthalimidopropiophenone and N-ethylcathinone (PubMed.gov / NCBI) | http://www.ncbi.nlm.nih.gov/pubmed/20074881
  3. Police warn of potentially fatal 'fake ecstasy' | http://www.abc.net.au/news/2008-06-17/police-warn-of-potentially-fatal-fake-ecstasy/2475270
  4. Cathinone derivatives: A review of their chemistry, pharmacology and toxicology | DOI 10.1002/dta.31
  5. Therapeutic potential of monoamine transporter substrates. | https://www.ncbi.nlm.nih.gov/pubmed/17017961
  6. Gillman, P. K. (2005). "Monoamine oxidase inhibitors, opioid analgesics and serotonin toxicity". British Journal of Anaesthesia. 95 (4): 434–441. doi:10.1093/bja/aei210Freely accessible. eISSN 1471-6771. ISSN 0007-0912. OCLC 01537271. PMID 16051647. 
  7. Talaie, H.; Panahandeh, R.; Fayaznouri, M. R.; Asadi, Z.; Abdollahi, M. (2009). "Dose-independent occurrence of seizure with tramadol". Journal of Medical Toxicology. 5 (2): 63–67. doi:10.1007/BF03161089. eISSN 1937-6995. ISSN 1556-9039. OCLC 163567183. 
  8. Gillman, P. K. (2005). "Monoamine oxidase inhibitors, opioid analgesics and serotonin toxicity". British Journal of Anaesthesia. 95 (4): 434–441. doi:10.1093/bja/aei210Freely accessible. eISSN 1471-6771. ISSN 0007-0912. OCLC 01537271. PMID 16051647. 
  9. Treatment for amphetamine psychosis | [1]
  10. Treatment for amphetamine psychosis | [2]
  11. Hofmann FG (1983). A Handbook on Drug and Alcohol Abuse: The Biomedical Aspects (2nd ed.). New York: Oxford University Press. p. 329. ISBN 9780195030570.
  12. Treatment for amphetamine psychosis | [3]
  13. Stimulant Misuse: Strategies to Manage a Growing Problem | http://www.acha.org/prof_dev/ADHD_docs/ADHD_PDprogram_Article2.pdf
  14. http://www.accessdata.fda.gov/drugsatfda_docs/label/2013/021303s026lbl.pdf
  15. "关于印发《非药用类麻醉药品和精神药品列管办法》的通知" (in Chinese). China Food and Drug Administration. 27 September 2015. Retrieved 1 October 2015. 
  16. Forbud mod tre nye stoffer | http://nyheder.tv2.dk/article.php/id-19197033.html?forside=
  17. Psychoactive Substances Act 2016 (Legislation.gov.uk) | http://www.legislation.gov.uk/ukpga/2016/2/contents/enacted