About Paracetamol api powder
| Grade Standard |
IP
|
| Packaging |
50Kg Drum
|
| CAS Number |
103-90-2
|
| Type |
Plain
|
| Grade |
Pharma Grade
|
| Usage/ Application |
Pharmaceutical
|
| Country of Origin |
Made in India
|
| Minimum Order Quantity |
25 Kg
|
High Purity and Stringent Quality ControlParacetamol API powder is quality-checked to ensure over 99% purity, with all impurities, such as related substances and heavy metals, strictly regulated under global pharmacopeial standards. Advanced analytical techniques, including IR and HPLC, guarantee product identity, while low levels of chloride, sulphate, and p-aminophenol support its pharmaceutical safety.
Versatile Application as Analgesic and AntipyreticThis active pharmaceutical ingredient is formulated for the manufacture of medicines intended to reduce pain and fever. Its consistent solid white, crystalline appearance, odorless nature, and slightly bitter taste enable integration into a variety of tablet, suspension, and syrup formulations, meeting the diverse needs of healthcare providers.
Safe Packaging and Long Shelf LifeEach batch is carefully packaged in food-grade HDPE drums with double polythene liners, preserving the powder's integrity during storage and transport. With appropriate handling and storage at temperatures below 25C, paracetamol API maintains its effectiveness for up to five years, ensuring reliability for bulk suppliers and manufacturers.
FAQ's of Paracetamol api powder:
Q: How is Paracetamol API powder identified and tested for quality?
A: Paracetamol API powder is identified and verified for quality using Infrared Spectroscopy (IR) and High-Performance Liquid Chromatography (HPLC), both of which must conform to standard specifications. These analytical methods ensure the product meets strict pharmaceutical requirements and is free from excessive impurities.
Q: What is the recommended storage condition for Paracetamol API powder, and why is it important?
A: The powder should be stored below 25C, protected from light and moisture. Proper storage maintains the stability, purity, and effectiveness of the product throughout its five-year shelf life, preventing degradation due to environmental exposure.
Q: Where is Paracetamol API powder typically used and by whom?
A: It is primarily used by pharmaceutical manufacturers, exporters, and suppliers in the production of analgesic and antipyretic medications. Its applications include tablets, suspensions, and syrups to provide relief from pain and fever.
Q: What benefits does pharmaceutical-grade Paracetamol API offer over other grades?
A: Pharmaceutical-grade Paracetamol API guarantees over 99% purity, low levels of impurities, and compliance with stringent microbial standards. This ensures the safety, consistency, and effectiveness of finished pharmaceutical products compared to lower-grade alternatives.
Q: How is Paracetamol API powder packaged for shipping and storage?
A: The product is securely packed in 25 kg high-density polyethylene (HDPE) drums with double polythene liners. This robust packaging protects the powder from contaminants, moisture, and light, ensuring safe transportation and long-term storage.
Q: When should Paracetamol API powder not be used?
A: It should not be used if the product shows signs of discoloration, contamination, or is past its expiration date. Adhering to recommended storage and handling conditions minimizes the risk of product degradation or compromised quality.
Q: What makes this Paracetamol API suitable for global pharmaceutical manufacturing?
A: Its compliance with international pharmacopoeial standards, high purity, low heavy metal content, controlled impurities, and robust quality assurance processes make it ideal for export and supply to regulated markets worldwide.