Independent · evidence-based · non-judgmentalDraft · pending medical review
Not yet medically reviewed — information on this site is in preparation and has not been verified by a medical reviewer.
Drug index / Dissociative / 2-FDCK
Dissociative

2-FDCK

2-(2-fluorophenyl)-2-(methylamino)cyclohexan-1-one

2-FDCK (2-fluorodeschloroketamine) is a synthetic dissociative and a close chemical analogue of ketamine sold as a research chemical. It is presumed to work like ketamine as an NMDA-receptor antagonist, but its pharmacology and safety in humans are largely unstudied — a key point of caution.

Overview

2-FDCK (2-fluorodeschloroketamine, also written 2F-DCK) is a synthetic dissociative of the arylcyclohexylamine class, closely related to ketamine — its structure is ketamine with the chlorine atom replaced by fluorine. It was first synthesized as part of research into ketamine analogues and appeared on the online "research chemical" market around 2016-2017, marketed as a legal ketamine substitute after another analogue (deschloroketamine) had been introduced. It is usually a powder that people snort or swallow. It has been detected in forensic, driving-under-the-influence, and wastewater samples in Europe and elsewhere.

Source: peer-reviewed forensic-toxicology literature

Chemistry & mechanism of action

2-FDCK is presumed to act like ketamine — as an antagonist at the NMDA glutamate receptor, the mechanism shared by ketamine, PCP, and MXE that produces the dissociative state. This is an important caveat: much of what is said about 2-FDCK's pharmacology is inferred from its close structural similarity to ketamine and from users' reported effects, rather than established by direct study. Its detailed receptor pharmacology in humans has not been well characterized, and it is best understood as "ketamine-like" by analogy rather than by evidence.

Source: peer-reviewed forensic-toxicology literature

Effects

Reported effects are described as similar to ketamine's: dissociation and detachment from body and surroundings, sedation, pain relief, altered perception, and at higher doses an immersive dissociative state. Because reliable human data are scarce, most descriptions come from user reports and isolated clinical case reports rather than controlled studies, so the picture of its effects — and how they differ from ketamine's — is incomplete.

Source: peer-reviewed forensic-toxicology literature

Risks & harms

The central risk with 2-FDCK is how little is known about it. As a dissociative it is expected to impair coordination and judgment, raising the risk of injury, and to carry the dependence potential common to NMDA-antagonist dissociatives, with cross-tolerance to ketamine and MXE. Because product strength varies and its potency relative to ketamine is not well established, dosing is uncertain and overdose is a real risk. Case reports document intoxications involving 2-FDCK, often alongside other drugs. Combining it with other depressants such as alcohol, benzodiazepines, or opioids is especially dangerous. The honest summary is that its long-term effects and safety profile in humans are essentially unknown.

Source: peer-reviewed forensic-toxicology literature

Images

Visual references coming soon.

If it’s too intense

If an experience becomes overwhelming, the goal is to stay safe and let it pass — most difficult experiences ease as the drug wears off.

  • Get to a calm, safe space with someone you trust who is sober and can stay with you.
  • Cool down if you’re overheating — move somewhere cool, remove extra layers, rest. Overheating is especially a risk with stimulants and MDMA.
  • Sip water to thirst — but don’t over-hydrate. Drinking large amounts of plain water (especially after MDMA) can dangerously dilute your blood sodium (hyponatremia). Electrolytes help more than volume.
  • Slow your breathing — long, slow exhales help settle a racing heart and anxiety.
  • A sugary drink, fruit juice, or a snack can ease shakiness and the anxiety that comes with low blood sugar.
  • Do not take more, and do not add another substance to manage it. Redosing or adding something else (including a sedative like a benzodiazepine) can make things worse, not better.

With dissociatives, coordination and judgment are impaired and effects can come in waves — sit or lie down somewhere safe so you don't fall, and don't drive or make decisions until it clears.

Call 911 (or Poison Control, 1-800-222-1222) right away for chest pain, a very high body temperature, a seizure, unconsciousness, or severe confusion. These are medical emergencies, not something to wait out.

Source: general harm-reduction guidance from SAMHSA, NIH/NIDA, and MedlinePlus, in our own words. Draft — not yet medically reviewed.

Forensic dossier

Draft · every field is source-cited or marked “Unknown — pending review”

Identity

IUPAC name
2-(2-fluorophenyl)-2-(methylamino)cyclohexan-1-one;hydrochloridePubChem PUG-REST · retrieved 2026-06-18
SMILES
CNC1(CCCCC1=O)C2=CC=CC=C2F.ClPubChem PUG-REST · retrieved 2026-06-18
InChIKey
FQOFLBNEXJTBJE-UHFFFAOYSA-NPubChem PUG-REST · retrieved 2026-06-18

Composition

Composition
N/A — single compound (see Identity)

Physical / pill characteristics

Dosage form
Unknown — pending review (no Rx/OTC label; illicit — pill visuals = FIRST-PARTY submissions only, never generated or scraped)
Route
Unknown — pending review
Shape
Unknown — pending review
Color
Unknown — pending review
Imprint
Unknown — pending review
Score
Unknown — pending review

Scheduling & legal status

US schedule
Unknown — pending review
International
See EMCDDA/EUDA + WHO — synthesize per jurisdictionEMCDDA / EUDA · retrieved 2026-06-18

Effects

Effects
Cited source pending synthesis — author in our words from NIDA/MedlinePlus on review (NOT auto-generated)NIDA + MedlinePlus · retrieved 2026-06-18

Risks

Risks
Cited source pending synthesis — author in our words from NIDA/MedlinePlus on review (NOT auto-generated)NIDA + MedlinePlus · retrieved 2026-06-18

Interactions

Interactions
Unknown — pending review

Dosage

Pending medical reviewer

Sources

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