About Dexchlorpheniramine API
Dexchlorpheniramine (dexchlorpheniramine systemic) is a member of the drug class antihistamines and is used to treat Allergic Reactions and Allergic Rhinitis.
| Name | DEXCHLORPHENIRAMINE MALEATE |
| Other Name | CHLORPHENIRAMINE MALEATE SALT |
| CAS No. | 2438-32-6 |
| MF | C20H23ClN2O4 |
| MW | 390.86 |
| MP | 112-115 |
| Storage temp. | Refrigerator |
| Purity | 99% min |
| Usage | The S-enantiomer of Chlorpheniramine; Antihistaminic. |
| Appearance | White Solid |
Packaging details:
| Packaging details: | 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum. |
| Storage: | Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat |
| Shelf Life: | 5 years if sealed and store away from direct sun light. |
Reliable Antihistamine IntermediateDexchlorpheniramine is a trusted active pharmaceutical ingredient (API) used in the development of antihistamine medicines. Its efficacy in treating allergies and related symptoms makes it a preferred choice among manufacturers and suppliers. Produced and distributed from India, it meets stringent quality standards for pharmaceutical use.
Consistent High Purity for Optimal ResultsEach batch of Dexchlorpheniramine undergoes rigorous quality control to ensure a consistent 99% purity. Its powder form and room temperature storage make handling and integration into pharmaceutical processes convenient and efficient, supporting large-scale production needs.
FAQ's of Dexchlorpheniramine API:
Q: How should Dexchlorpheniramine powder be stored to maintain its stability?
A: Dexchlorpheniramine should be stored at room temperature in a well-sealed container, away from moisture and direct sunlight. Proper storage helps preserve its white solid appearance and high potency.
Q: What is the primary usage of Dexchlorpheniramine as a pharmaceutical intermediate?
A: Dexchlorpheniramine serves as an antihistamine intermediate, widely used in the formulation of medicines designed to manage and alleviate allergic reactions, such as hay fever, urticaria, and other allergy-related symptoms.
Q: When is Dexchlorpheniramine typically incorporated into pharmaceutical products?
A: This API is incorporated during the manufacturing phases of pharmaceutical products that require antihistamine properties, most often in preparations targeting relief from allergies.
Q: Where is Dexchlorpheniramine API manufactured and supplied from?
A: Dexchlorpheniramine is manufactured and distributed from India, where it is available through multiple channels including distributor, exporter, manufacturer, supplier, trader, and wholesaler networks.
Q: What is the process of using Dexchlorpheniramine in pharmaceutical formulation?
A: Dexchlorpheniramine is integrated as a powder into drug development pipelines, where it acts as a core ingredient for antihistamine medicinal products. Its high purity and stable form ensure effective transformation into final dosage forms.
Q: What benefits does Dexchlorpheniramine offer to pharmaceutical manufacturers?
A: Manufacturers benefit from its consistent 99% purity, ease of handling due to its stable powder form, and proven effectiveness as an antihistamine intermediate, enabling production of reliable and potent allergy treatments.