77179-39-6

Basic information

• Product Name: 1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol
• Synonyms: 1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol
• CAS NO: 77179-39-6
• Molecular Formula: C₂₃H₂₉NO
• Molecular Weight: 335.48
• Mol File: 77179-39-6.mol
• Article Data: 1

Chemical Properties

• Melting Point: 103-105 °C(Solv: ethyl acetate (141-78-6))
• Boiling Point: 494.9°C at 760 mmHg
• Flash Point: 101.1°C
• Appearance: /
• Density: 1.118g/cm³
• Vapor Pressure: 1.3E-10mmHg at 25°C
• Refractive Index: 1.6
• PKA: 14.05±0.20(Predicted)
• CAS DataBase Reference: 1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol(77179-39-6)
• EPA Substance Registry System: 1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol(77179-39-6)

Safety Data

• Hazardous Substances Data: 77179-39-6(Hazardous Substances Data)

Usage

Description

1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol, commonly known as PCP or angel dust, is a dissociative drug with hallucinogenic properties. It is a white crystalline powder that is often used recreationally for its mind-altering effects. PCP acts as a potent central nervous system depressant, leading to distorted perceptions of sight and sound, as well as a sense of detachment from one's environment.

Uses

Used in Recreational Drug Use:
1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol is used as a recreational drug for its hallucinogenic and dissociative effects. It is often smoked, snorted, or ingested by users seeking altered states of consciousness and sensory experiences.
However, it is important to note that the use of PCP is illegal in most parts of the world due to its dangerous side effects and potential for addiction. These side effects can include paranoia, aggression, violent behavior, and severe psychological and physical health issues when used long-term.
Please be aware that the use of PCP and its associated risks are not endorsed or recommended. The information provided is for educational purposes only and should not be taken as encouragement for the use of illegal substances.

InChI:InChI=1/C23H29NO/c25-23(21-12-6-2-7-13-21)16-18-24(19-17-23)22(14-8-3-9-15-22)20-10-4-1-5-11-20/h1-2,4-7,10-13,25H,3,8-9,14-19H2

Upstream product

• 344260-33-9 1-(4-Trimethylsilanyloxy-piperidin-1-yl)-cyclohexanecarbonitrile 
• 60232-85-1 1-(1-phenylcyclohexyl)-4-hydroxypiperidine 
• 77179-42-1 1-(1-phenylcyclohexyl)-4-piperidone 
• 591-51-5 phenyllithium 

Downstream Products

• 77179-40-9 1-(1-phenylcyclohexyl)-4-phenyl-4-piperidyl propionate 

Relevant articles and documents

New Analgesic Drugs Derived from Phencyclidine

Several esters of 1-(1-phenylcyclohexyl)-4-piperidinol (3), 1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol (10) and its propionate (11), and 1-(1-phenylcyclohexyl)-4-phenylpiperidine (13) were prepared and characterized.The new compounds, which are derived from phencyclidine, exerted analgesic activity in mice.The most potent is 10, which is twice as active as morphine.The antinociceptive activity of 10, 11, and 13 could be well correlated with their potency in the mouse vas deferens bioassay, and both were completely reversed by naloxone.