azaperol

Names

[ CAS No. ]:
2804-05-9

[ Name ]:
azaperol

[Synonym ]:
1-(4-Fluorphenyl)-4-<4-(2-pyridyl)piperazino>butan-1-ol
1-(4-fluoro-phenyl)-4-(4-pyridin-2-yl-piperazin-1-yl)-butan-1-ol
Azaperol
|A-(4-Fluorophenyl)-4-(2-pyridinyl)-1-piperazinebutanol

Chemical & Physical Properties

[ Density]:
1.177g/cm3

[ Boiling Point ]:
501.7ºC at 760 mmHg

[ Molecular Formula ]:
C19H24FN3O

[ Molecular Weight ]:
329.41200

[ Flash Point ]:
257.2ºC

[ Exact Mass ]:
329.19000

[ PSA ]:
39.60000

[ LogP ]:
2.85940

[ Vapour Pressure ]:
6.95E-11mmHg at 25°C

[ Index of Refraction ]:
1.577

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Faceshields;Gloves

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
22

[ Safety Phrases ]:
6-20-62

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
29335990

Synthetic Route

Precursor & DownStream

Precursor

  • Azaperone

DownStream

Articles

Simultaneous determination of azaperone and azaperol in animal tissues by HPLC with confirmation by electrospray ionization mass spectrometry

J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 877(3) , 166-72, (2009)

A simple method is described for the determination of azaperone and its metabolite, azaperol, in animal tissues by high-performance liquid chromatography with ultraviolet detection (HPLC/UV). Chromato...

Gas chromatographic-mass spectrometric analysis of veterinary tranquillizers in urine: evaluation of method performance.

J. Chromatogr. B. Biomed. Sci. Appl. 734(1) , 113-20, (1999)

A method for analysis of veterinary tranquillizers in urine using gas chromatography-mass spectrometry (GC-MS) is described. Detection limits are 5 microg/l for ketamine, azaperone and the phenothiazi...

Evaluation of the effects of the enantiomers of reduced haloperidol, azaperol, and related 4-amino-1-arylbutanols on dopamine and sigma receptors.

J. Med. Chem. 36(24) , 3929-36, (1993)

The enantiomers of reduced haloperidol (3a), azaperol (3b), and the related compound BMY-14802 (3c) were prepared in high optical purity. The affinity of these compounds for dopamine D2 and D3 recepto...


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