ChemicalBook--->CAS DataBase List--->2448-68-2

2448-68-2

2448-68-2 Structure

2448-68-2 Structure
IdentificationBack Directory
[Name]

PipaMperone Dihydrochloride
[CAS]

2448-68-2
[Synonyms]

Nsc170981
carpiperone
fluoropipamide
Pipamperone 2HCl
Pipamperone DiHCl
Pipamperone hydrochloride
floropipamide hydrochloride
PIPAMPERONE DIHYDROCHLORIDE
Pipamperone dihydrochloride salt
R4050, 1μ-[4-(4-Fluorophenyl)-4-oxobutyl]-[1,4μ-bipiperidine]-4μ-carboxamide dihydrochloride
[EINECS(EC#)]

219-507-5
[Molecular Formula]

C21H30FN3O2.2ClH
[MDL Number]

MFCD00242980
[MOL File]

2448-68-2.mol
Chemical PropertiesBack Directory
[Melting point ]

203-218°C
[storage temp. ]

Hygroscopic, Refrigerator, Under Inert Atmosphere
[solubility ]

H2O: ~50mg/mL
[form ]

powder
[color ]

white
[Water Solubility ]

H2O: >2.0mg/mL
[Stability:]

Hygroscopic
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

1
[RTECS ]

DW1060000
[Toxicity]

mouse,LD50,intravenous,71mg/kg (71mg/kg),Drugs in Japan Vol. 6, Pg. 631, 1982.
Hazard InformationBack Directory
[Chemical Properties]

Off-White to Pale Yellow Solid
[Uses]

Antipsychotic.
[Uses]

Pipamperone dihydrochloride may be used:
  • as an internal standard in liquid chromatography with coulometric detection
  • as an antipsychotic drugs to test its interaction with human ether-a-go-go-related gene (hERG) channel
  • as an internal standard to spike human colostrum samples for reversed phase liquid chromatography- ultraviolet (LC-UV) analysis

[Definition]

ChEBI: A hydrochloride resulting from the reaction of pipamperone with 2 mol eq. of hydrogen chloride. It is used as an antipsychotic.
[Biochem/physiol Actions]

Pipamperone, a butyrophenone derivative is a pharmacological chaperone and is a membrane-permeable dopamine receptor D4 (DRD4) antagonist. The affinity of pipamperone is higher for DRD4 and 5-hydroxytryptamine 2A receptor (5-HT2A) in comparison with DRD2. It may be useful therapeutic in treating behavioral disorders and psychomotor agitation symptoms.
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