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Levocetirizine Dihydrochloride

Catalog No. T22354Cas No. 130018-87-0
Alias Xyzal Dihydrochloride, (-)-Cetirizine Dihydrochloride

Levocetirizine Dihydrochloride (Xyzal Dihydrochloride) is a third-generation peripheral H1-receptor antagonist. Acting as an antihistaminic agent, it specifically targets the histamine H1-receptor. Levocetirizine Dihydrochloride is the R-enantiomer of Cetirizine, which gives it a higher affinity for the H1-receptor than the S-enantiomer. Due to this enhanced affinity, Levocetirizine Dihydrochloride is effective in treating allergic rhinitis and chronic idiopathic urticaria.

Levocetirizine Dihydrochloride

Levocetirizine Dihydrochloride

Purity: 99.75%
Catalog No. T22354Alias Xyzal Dihydrochloride, (-)-Cetirizine DihydrochlorideCas No. 130018-87-0
Levocetirizine Dihydrochloride (Xyzal Dihydrochloride) is a third-generation peripheral H1-receptor antagonist. Acting as an antihistaminic agent, it specifically targets the histamine H1-receptor. Levocetirizine Dihydrochloride is the R-enantiomer of Cetirizine, which gives it a higher affinity for the H1-receptor than the S-enantiomer. Due to this enhanced affinity, Levocetirizine Dihydrochloride is effective in treating allergic rhinitis and chronic idiopathic urticaria.
Pack SizePriceAvailabilityQuantity
10 mg$43In Stock
25 mg$78In Stock
50 mg$133In Stock
100 mg$198In Stock
200 mg$297In Stock
500 mg$513In Stock
1 g$729In Stock
1 mL x 10 mM (in DMSO)$48In Stock
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Purity:99.75%
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Product Introduction

Bioactivity
Description
Levocetirizine Dihydrochloride (Xyzal Dihydrochloride) is a third-generation peripheral H1-receptor antagonist. Acting as an antihistaminic agent, it specifically targets the histamine H1-receptor. Levocetirizine Dihydrochloride is the R-enantiomer of Cetirizine, which gives it a higher affinity for the H1-receptor than the S-enantiomer. Due to this enhanced affinity, Levocetirizine Dihydrochloride is effective in treating allergic rhinitis and chronic idiopathic urticaria.
In vivo
Levocetirizine (0.4 mg/kg; oral administration; male Sprague-Dawley rats) yields a Cmax of 0.34 μg/mL, an AUC0-t of 3.26 μg h/mL, an AUC0-∞ of 3.67 μg h/mL, and a t1/2 of 2.34 hours in Sprague-Dawley rats[1].
AliasXyzal Dihydrochloride, (-)-Cetirizine Dihydrochloride
Chemical Properties
Molecular Weight461.81
FormulaC21H27Cl3N2O3
Cas No.130018-87-0
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 90 mg/mL (194.9 mM), Sonication is recommended.
DMSO: 50 mg/mL (108.27 mM), Sonication is recommended.
Solution Preparation Table
DMSO/H2O
1mg5mg10mg50mg
1 mM2.1654 mL10.8270 mL21.6539 mL108.2696 mL
5 mM0.4331 mL2.1654 mL4.3308 mL21.6539 mL
10 mM0.2165 mL1.0827 mL2.1654 mL10.8270 mL
20 mM0.1083 mL0.5413 mL1.0827 mL5.4135 mL
50 mM0.0433 mL0.2165 mL0.4331 mL2.1654 mL
100 mM0.0217 mL0.1083 mL0.2165 mL1.0827 mL

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Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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