Ethcathinone

Price range: $450.00 through $8,700.00

WeightPrice
100 g$450.00
200 g$670.00
300 g$810.00
400 g$900.00
500 g$960.00
600 g$1,090.00
700 g$1,215.00
800 g$1,345.00
900 g$1,470.00
1000 g$1,600.00
2000 g$2,390.00
3000 g$3,180.00
5000 g$4,755.00
10000 g$8,700.00
SKU: Ethcathinone Category:

Ethcathinone, also known as ethylcathinone or ethylpropion, is a synthetic cathinone stimulant. It is the N-ethyl analogue of cathinone and is structurally related to methcathinone. The compound has been studied in laboratory experiments on monoamine transporters, but there is little controlled information about its effects or toxicity in humans.

Chemistry

Ethcathinone is a β-keto amphetamine with an ethyl group attached to the amino nitrogen. It differs from methcathinone, which has an N-methyl group, and from cathinone, which has a primary amine. The additional carbonyl group on the beta carbon distinguishes cathinones from their corresponding amphetamine analogues.

Pharmacology

In a study of designer cathinones, ethcathinone inhibited norepinephrine and dopamine uptake and promoted norepinephrine release. The study did not find the same dopamine-releasing effect observed with some other stimulants in the series. This profile is consistent with a stimulant mechanism involving monoamine transporters, although the results were obtained in experimental systems rather than in humans (Simmler and colleagues, 2014).

The broader study also showed that cathinones differ considerably in their effects on dopamine, norepinephrine and serotonin transporters. The pharmacology of one compound should therefore not be assumed to apply to another simply because they share the cathinone core.

Reported effects

Reliable human evidence is too scarce to establish a characteristic ethcathinone experience. Its laboratory profile supports stimulant activity, but detailed reports of euphoria, focus, sociability or sensory changes are sparse and have not been confirmed in controlled studies.

Potential effects such as increased wakefulness, restlessness and cardiovascular stimulation are consistent with the broader stimulant class. They should not be presented as a well-established list of compound-specific effects.

Toxicity and research limitations

Human toxicological information on ethcathinone is limited. The available laboratory study provides evidence of monoamine-transporter activity, but does not establish its acute toxic range, dependence potential or long-term effects. There is also insufficient information to define a reliable interaction profile.

Clinical findings from methcathinone and other cathinones may help explain the broader risks of stimulant exposure, but they cannot substitute for direct research on ethcathinone.

Related compounds

Ethcathinone is related to Cathinone, Methcathinone and 4-MEC. It is the N-ethyl analogue of cathinone and differs from methcathinone by the additional carbon in the nitrogen substituent.

Weight

100 g, 200 g, 300 g, 400 g, 500 g, 600 g, 700 g, 800 g, 900 g, 1000 g, 2000 g, 3000 g, 5000 g, 10000 g

Identity and Structure

Chemical NameEthcathinone
Catalog Entity TypeCompound
FormulaC11H15NO
Molar Mass177.247 g·mol−1
CAS18259-37-5
51553-17-4
CAS Numbers and Substance Forms18259-37-5
hydrochloride: 51553-17-4
SynonymsN-Ethylcathinone; 2-Ethylaminopropiophenone
IUPAC Name(RS)-2-ethylamino-1-phenyl-propan-1-one
InChIInChI=1S/C11H15NO/c1-3-12-9(2)11(13)10-7-5-4-6-8-10/h4-9,12H,3H2,1-2H3
InChIKeyLYMHIBZGTAPASQ-UHFFFAOYSA-N
SMILESO=C(c1ccccc1)C(NCC)C
ChiralityRacemic mixture

Chemical Identifiers

PubChem CID458519
ChemSpider ID403504
KEGG IDC22705
UNIIHV3BCK77BB
SQ59TT7X5R
IUPHAR/BPS ID7398
CompTox DTXSIDDTXSID70939595

Physical Properties

Melting Point195 to 198 °C (383 to 388 °F) (hydrochloride)
Boiling Point272.3 °C (522.1 °F) at 760 mmHg (hydrochloride)

Clinical Data

Drug ClassNorepinephrine releasing agent
Routes of AdministrationBy mouth, intranasal
ATC Codenone

Legal Status

Legal Status (Wikipedia Source Text)BR: Class F2 (Prohibited psychotropics)
DE: Anlage II (Authorized trade only, not prescriptible)
UK: Class B
US: Schedule I

Sources and Attribution

Wikipedia Source URLhttps://en.wikipedia.org/?curid=14807023
Wikipedia Retrieval Date2026-10-21T19:55:21+00:00

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