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Basic Information
CAS No.: 26864-56-2
Name: Penfluridol
Molecular Structure:
Molecular Structure of 26864-56-2 (Penfluridol)
Formula: C28H27ClF5NO
Molecular Weight: 523.973
Synonyms: 4-Piperidinol,1-[4,4-bis(p-fluorophenyl)butyl]-4-(4-chloro-a,a,a-trifluoro-m-tolyl)- (8CI);1-[4,4-Bis(p-fluorophenyl)butyl]-4-(4-chloro-a,a,a-trifluoro-m-tolyl)-4-piperidinol;McN-JR 16341;Penfluridol;R 16341;Semap;
EINECS: 248-074-5
Density: 1.29 g/cm3
Melting Point: 105-107 °C
Boiling Point: 587.7 °C at 760 mmHg
Flash Point: 309.2 °C
Solubility: Insoluble in water
Appearance: white powder
Hazard Symbols: ToxicT
Risk Codes: 25
Safety: 45
Transport Information: UN 2811
PSA: 23.47000
LogP: 7.47060
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    Overview Quick Details CAS No.: 26864-56-2 Other Names: Penfluridol MF: C28H27ClF5NO EINECS No.: NA Place of Origin: Shaanxi, China (Mainland) Type: Antibiotic and Antimicrobial Agents, Other Grade Standard: Medicine Grade, T

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Chemistry

Molecular Formula: C28H27ClF5NO
Molecular Weight; 523.97
EINECS: 248-074-5
Density: 1.29 g/cm3
Storage temp: 2-8°C
Flash Point: 309.2 °C
Solubility: H2O: insoluble
Appearance: white powder
Melting point  105-107 ºC
Index of Refraction: 1.552 
Enthalpy of Vaporization: 92.29 kJ/mol 
Boiling Point: 587.7 °C at 760 mmHg 
Vapour Pressure: 1.17E-14 mmHg at 25°C
Product Categories: API intermediates
IUPAC Name: 1-[4,4-bis(4-fluorophenyl)butyl]-4-[4-chloro-3-(trifluoromethyl)phenyl]piperidin-
4-ol
Synonyms  1-[4,4-Bis(4-fluorophenyl)butyl]-4-[4-chloro-3(trifluoromethyl)phenyl]-4-piperidinol
Following is the molecular structure of Penfluridol (26864-56-2):

Uses

Penfluridol (26864-56-2)is a oral long-acting antipsychotics.It is applicable to all types of mental illness.

Toxicity Data With Reference

1.    

orl-rat TDLo:3 mg/kg (lactating female 3D post):REP

    NSAPCC    Naunyn-Schmiedeberg’s Archives of Pharmacology. 279 (1973),31.
2.    

orl-mus TDLo:48 mg/kg (7-12D preg):TER

    OYYAA2    Oyo Yakuri. Pharmacometrics. 13 (1977),581.
3.    

orl-rat LD50:160 mg/kg

    EJPHAZ    European Journal of Pharmacology. 11 (1970),139.
4.    

orl-mus LD50:87 mg/kg

    EJPHAZ    European Journal of Pharmacology. 11 (1970),139.
5.    

orl-gpg LD50:90 mg/kg

    EJPHAZ    European Journal of Pharmacology. 11 (1970),139.

Safety Profile

Poison by ingestion and intravenous routes. Experimental teratogenic and reproductive effects. A neuroleptic agent. When heated to decomposition it emits very toxic fumes of Cl, F, and NOx.
Safety Information of Penfluridol (26864-56-2):
Hazard Codes: T
T: Toxic
Risk Statements: 25
25: Toxic if swallowed 
Safety Statements: 45
45: In case of accident or if you feel unwell, seek medical advice immediately (show label where possible)  
RIDADR: UN 2811 6.1/PG 3
WGK Germany: 3
RTECS: TN6957000

Specification


Penfluridol (26864-56-2) is a highly potent, first generation diphenylbutylpiperidine antipsychotic Related to other diphenylbutylpiperidine antipsychotics, pimozide and fluspirilene, penfluridol has an extremely long elimination half-life and its effects last for many days after single oral dose. Its antipsychotic potency, in terms of dose needed to produce comparable effects, is similar to both haloperidol and pimozide. It is only slightly sedative, but often causes extrapyramidal side-effects, such as akathisia, dyskinesiae and pseudo-Parkinsonism. Penfluridol is indicated for antipsychotic treatment of chronic schizophrenia and similar psychotic disorders, it is, however, like most typical antipsychotics, being increasingly replaced by the atypical antipsychotics. Due to its extremely long lasting effects, it is often prescribed to be taken orally as tablets only once a week (q 7 days). The once-weekly dosis is usually 10 — 60 mg.