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ChemicalBook--->CAS DataBase List--->2070015-04-0

2070015-04-0

2070015-04-0 Structure

2070015-04-0 Structure
IdentificationBack Directory
[Name]

Cetirizine-d8 (hydrochloride)
[CAS]

2070015-04-0
[Synonyms]

Cetirizine-d8 DiHCl
Cetirizine-d8 (hydrochloride)
[2H8]-Cetirizine Dihydrochloride
[Molecular Formula]

C21H18Cl2D8N2O3
[MOL File]

2070015-04-0.mol
[Molecular Weight]

433.398
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Methanol: slightly soluble; Water: slightly soluble
[form ]

A solid
[Stability:]

Hygroscopic
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501
Hazard InformationBack Directory
[Description]

Cetirizine-d8 (hydrochloride) is intended for use as an internal standard for the quantification of cetirizine , (R)-cetirizine , and (S)-cetirizine by GC- or LC-MS. Cetirizine is a bioactive carboxylated metabolite of hydroxyzine that acts as a selective histamine H1 receptor antagonist (Ki = 10 nM). As a second generation antihistamine, it is non-sedating due to low lipophilicity, which prevents blood-brain barrier transit. Cetirizine is a racemic mixture composed of equal amounts of two enantiomers, (R)-cetirizine and (S)-cetirizine, with pharmacological activity residing primarily in the (R) isomer. Cetirizine inhibits eosinophil chemotaxis and leukotriene B4 (LTB4; ) release independent from H1 antagonism. It inhibits aerosol histamine-induced bronchospasm in guinea pigs (ED50 = 100 μg/kg, p.o.). Formulations containing cetirizine have been used in the treatment of allergic rhinitis and chronic urticaria.
[Uses]

A nonsedating type histamine H1-receptor antagonist. A major metabolite of Hydroxyzine. Pharmacological activity resides primarily in the (R)-isomer. Antihystaminic.
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