
Dexchlorpheniramine maleate
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Category:Active Pharmaceutical Ingredients Own Brand:MT /MOQ:100KG /From China/ B2B only.
Introduction
Catalog ID80019499
CAS NO.2438-32-6
Purity 98%
MDL NumberMFCD00079046
EINEC219-450-6
Molecular FormulaC16H19ClN2.C4H4O4
Molecular Weight390.865
Melting point: 113~117°C
| Category | Details |
|---|---|
| Chemical Properties | White or almost white, crystalline powder. It is a white, odorless crystalline powder with a pH of 4.0–5.0 in aqueous solution. |
| Solubility | Very soluble in water, freely soluble in ethanol (96%), methanol, and methylene chloride. |
| Mechanism of Action | Dexchlorpheniramine maleate is a first-generation histamine H1 antagonist. It competes with histamine for H1-receptor sites on effector cells in the gastrointestinal tract, blood vessels, and respiratory tract, thereby preventing histamine-induced symptoms such as sneezing, watery eyes, and runny nose. |
| Pharmacokinetics | Orally administered dexchlorpheniramine has an oral bioavailability of 40.5% in rats. It is primarily metabolized in the liver by CYP2D6, with minor contributions from CYP3A4, CYP2C11, and CYP2B1. It is excreted renally. |
| Storage Conditions | Store at 2–8°C. |
| Safety and Handling | Classified as toxic if swallowed. It may cause allergic skin reactions and serious eye damage. Wear protective clothing, gloves, and eye/face protection when handling |
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