Identification | Back Directory | [Name]
PHENCYCLIDINE HYDROCHLORIDE | [CAS]
956-90-1 | [Synonyms]
trank sernyl gp-121 mcv4158 nih9580 elysion sernylan nsc-40902 cn-25,253-2 pcphydrochloride sernylhydrochloride PHENCYCLIDINE HYDROCHLORIDE phenylcyclidinehydrochloride phencyclidinemonohydrochloride PHENCYCLIDINE HYDROCHLORIDE (PCP) >97% Phencyclidine Hydrochloride CII (25 mg) (AS) 1-(1-phenylcyclohexyl)-piperidinhydrochloride 1-[1-PHENYLCYCLOHEXYL]PIPERIDINE HYDROCHLORIDE Piperidine, 1-(1-phenylcyclohexyl)-, hydrochloride 1-(1-Phenylcyclohexyl)piperidine hydrochloride, PCP hydrochloride | [Molecular Formula]
C17H26ClN | [MDL Number]
MFCD00058208 | [MOL File]
956-90-1.mol | [Molecular Weight]
279.85 |
Questions And Answer | Back Directory | [Description]
Phencyclidine hydrochloride (PCP) is a psychoactive drug that has inhibitory, excitatory, analgesic and hallucinogenic effects on the central nervous system. Its chemical name is 1-(1-phenylcyclohexane)piperidine. It is a dissociative drug once used by anesthesiologists as an anesthetic with hallucinogenic and neurotoxic effects. |
Hazard Information | Back Directory | [Chemical Properties]
Crystalline Solid | [Uses]
Anesthetic (intravenous).
Controlled substance (depressant). | [Uses]
Controlled substance (depressant). Anesthetic (intravenous). | [Biological Activity]
Non-competitive NMDA receptor antagonist and sigma receptor agonist. Psychostimulant; induces rotational behavior, head-weaving and cognitive dysfunction in rats. | [Brand name]
Sernylan (Parke-Davis). | [Biochem/physiol Actions]
σ opioid receptor agonist and psychostimulant; inhibits NMDA glutamate receptor activation by binding to an allosteric site within the ion channel. | [Safety Profile]
Poison by ingestion,subcutaneous, intravenous, and intraperitoneal routes.Human systemic effects by ingestion and intravenousroutes: distorted perceptions, euphoria, excitement,hallucinations, and paresthesia. An experimental teratogen.Other experime | [storage]
Store at RT |
Safety Data | Back Directory | [Hazard Codes ]
T | [Risk Statements ]
25 | [Safety Statements ]
36/37-45 | [RIDADR ]
UN 2811 6.1/PG 3
| [WGK Germany ]
3
| [RTECS ]
TN2272600
| [HazardClass ]
6.1(a) | [PackingGroup ]
I | [HS Code ]
2933330000 | [Toxicity]
LD50 orally in mice: 76.5 mg/kg (Bailey) |
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