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956-90-1

956-90-1 Structure

956-90-1 Structure
IdentificationBack 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 AnswerBack 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.
Chemical PropertiesBack Directory
[Appearance]

Crystalline Solid
[Melting point ]

233-235°C
[Boiling point ]

135-137°C
[storage temp. ]

Store at RT
[solubility ]

H2O: 11.2 mg/mL
[form ]

Solid
[color ]

Crystals
[Water Solubility ]

Soluble to 40 mM in water
[EPA Substance Registry System]

Piperidine, 1-(1-phenylcyclohexyl)-, hydrochloride (956-90-1)
Hazard InformationBack 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 DataBack 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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