| Identification | More | [Name]
Cloperastine hydrochloride | [CAS]
14984-68-0 | [Synonyms]
1-[2-[(4-chlorophenyl)phenylmethoxy]ethyl]piperidinium chloride
4-CHLOROBENZHYDRYL 2-[1-PIPERIDYL]-ETHYL ETHER HYDROCHLORIDE
CHLOPERASTINE HYDROCHLORIDE
CLOPERASTINE HCL
CLOPERASTINE HYDROCHLORIDE
1-(2-((p-chloro-alpha-phenylbenzyl)oxy)ethyl)piperidinehydrochloride
1-(2-((p-chloro-alpha-phenylbenzyl)oxy)ethyl)-piperidinhydrochloride
1-(2-(p-cloro-alpha-fenilbenzilossi)etil)piperidinacloridrato
2-piperidinoethylp-chlorobenzhydryletherhydrochloride
cloperastinacloridrato
ht11
hustazol
4-chlorobenzhydryl 2-(1-piperidyl)ethyl ether | [EINECS(EC#)]
239-067-8 | [Molecular Formula]
C20H25Cl2NO | [MDL Number]
MFCD00079012 | [Molecular Weight]
366.32 | [MOL File]
14984-68-0.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed. | [Safety Statements ]
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [RTECS ]
TM6491500
| [HS Code ]
2933.39.9200 |
| Hazard Information | Back Directory | [Uses]
Antitussive;'Histamine antagonist | [Definition]
ChEBI: Cloperastine hydrochloride is a diarylmethane. | [in vivo]
In the anesthetized guinea pigs, Cloperastine at a therapeutic dose of 1 mg/kg prolonged the QT interval and monophasic?
action potential (MAP) duration without affecting PR interval or QRS width[1].
?
Cloperastine hydrochloride shows relatively low acute toxicity when administered by the intraperitoneal route in rats and mice, and shows minor toxicity by the oral route when administered as Cloperastine fendizoate, the LD50 in rats and mice for the two administration routes exceeds 1000 and 2000 mg/kg, respectively[2]. |
|
|