Understanding Desloratadine Chemical Properties for Pharmaceutical Applications
The efficacy of any pharmaceutical product hinges on the quality and understanding of its active ingredients. Desloratadine (CAS 100643-71-8), a crucial component in modern allergy treatments, possesses specific chemical properties that make it an ideal candidate for pharmaceutical formulations. NINGBO INNO PHARMCHEM CO.,LTD. provides high-purity Desloratadine, ensuring that manufacturers have access to a material that meets exacting standards.
Desloratadine is characterized by its chemical formula C19H19ClN2 and a molecular weight of approximately 310.83 g/mol. In its pure form, it typically presents as a white crystalline powder. This physical state is advantageous for pharmaceutical manufacturing, allowing for easy handling, precise dosing, and effective formulation into various dosage forms, such as tablets and oral solutions. The crystalline nature also contributes to its stability, a critical factor for drug shelf-life and efficacy.
The pharmacological action of Desloratadine as a selective H1-antihistamine is directly linked to its molecular structure. It acts as an inverse agonist at the histamine H1 receptor, effectively blocking the effects of histamine, a key mediator in allergic reactions. Unlike some older antihistamines, Desloratadine exhibits minimal affinity for muscarinic, adrenergic, or serotonergic receptors, which contributes to its favorable side-effect profile, particularly the absence of significant drowsiness. This selectivity is a direct result of its chemical design.
For pharmaceutical companies, understanding the desloratadine chemical properties also involves considering its solubility and stability under various conditions. While specific solubility data can vary, it is generally soluble in certain organic solvents, which is important for extraction and purification processes during manufacturing. NINGBO INNO PHARMCHEM CO.,LTD. ensures that our desloratadine active pharmaceutical ingredient is processed to maintain optimal stability, adhering to GMP, FDA, and ISO guidelines. This focus on the desloratadine pharmaceutical grade means our clients receive a product ready for immediate incorporation into their manufacturing workflows.
The precise control over the desloratadine 100643-71-8 manufacturing process at NINGBO INNO PHARMCHEM CO.,LTD. guarantees a high assay, typically exceeding 99%. This level of purity is essential for ensuring the safety and efficacy of the final drug product. By providing well-characterized and consistently high-quality Desloratadine, we empower our clients to develop and produce advanced allergy medications that meet the needs of patients worldwide. We invite you to explore the quality and advantages of our desloratadine pharmaceutical ingredient by contacting us for samples and detailed technical information.
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Future Origin 2025
“ensures that our desloratadine active pharmaceutical ingredient is processed to maintain optimal stability, adhering to GMP, FDA, and ISO guidelines.”
Core Analyst 01
“This focus on the desloratadine pharmaceutical grade means our clients receive a product ready for immediate incorporation into their manufacturing workflows.”
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“The precise control over the desloratadine 100643-71-8 manufacturing process at NINGBO INNO PHARMCHEM CO.”