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CAS

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77179-39-6

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.

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  • 77179-39-6 Structure

  • Basic information

    1. Product Name: 1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol
    2. Synonyms: 1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol
    3. CAS NO:77179-39-6
    4. Molecular Formula: C23H29NO
    5. Molecular Weight: 335.48
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 77179-39-6.mol

  • Chemical Properties

    1. Melting Point: 103-105 °C(Solv: ethyl acetate (141-78-6))
    2. Boiling Point: 494.9°C at 760 mmHg
    3. Flash Point: 101.1°C
    4. Appearance: /
    5. Density: 1.118g/cm3
    6. Vapor Pressure: 1.3E-10mmHg at 25°C
    7. Refractive Index: 1.6
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 14.05±0.20(Predicted)
    11. CAS DataBase Reference: 1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol(CAS DataBase Reference)
    12. NIST Chemistry Reference: 1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol(77179-39-6)
    13. EPA Substance Registry System: 1-(1-phenylcyclohexyl)-4-phenyl-4-piperidinol(77179-39-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 77179-39-6(Hazardous Substances Data)

77179-39-6 Usage

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.

Check Digit Verification of cas no

The CAS Registry Mumber 77179-39-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,7 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77179-39:
(7*7)+(6*7)+(5*1)+(4*7)+(3*9)+(2*3)+(1*9)=166
166 % 10 = 6
So 77179-39-6 is a valid CAS Registry Number.
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

77179-39-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenyl-1-(1-phenylcyclohexyl)piperidin-4-ol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:77179-39-6 SDS

77179-39-6Relevant articles and documents

New Analgesic Drugs Derived from Phencyclidine

Itzhak, Yossef,Kalir, Asher,Weissman, Ben Avi,Cohen, Sasson

, p. 496 - 499 (2007/10/02)

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.

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