About Croscarmellose Sodium
Crosscarmellose Sodium
- Other Name : Sodium CarboxyMethtylCellulose
- CAS Number : 74811-65-7
- Molecular Formula : C12H10CA3O14.4H20
- Application : Used as Disintegrant in Capsules, Tablet and Granule Formulations.
Superdisintegrant for Enhanced Tablet PerformanceCroscarmellose Sodium dramatically improves the dissolution and bioavailability of active pharmaceutical ingredients in tablets. Its crosslinked structure allows for exceptional swelling properties when exposed to moisture, ensuring tablets disintegrate rapidly upon ingestion for optimal therapeutic effect. This makes it a preferred choice among formulators for fast-acting and reliable oral dosage forms.
Strict Quality and Safety StandardsEvery batch complies with pharmaceutical-grade requirements: bulk density of 0.450.55 g/cm, residue on ignition of 8.010.0%, and stringent microbial limits. It is tasteless, odorless, and non-poisonous, making it safe for use in oral solid dosage forms. Sourced, manufactured, and supplied by trusted distributors and exporters in India, the product conforms to CAS No: 74811-65-7 and EINECS No: 277-098-7.
Applications in Diverse IndustriesBeyond pharmaceuticals, Croscarmellose Sodium is utilized in nutraceuticals and the food industry as a functional excipient. Its grade, purity, and safety profile make it suitable for bulk supply, supporting manufacturers, traders, wholesalers, and retailers who demand consistent quality for their end products.
FAQs of Croscarmellose Sodium:
Q: How does Croscarmellose Sodium act as a superdisintegrant in tablet formulations?
A: Croscarmellose Sodium, due to its crosslinked structure, swells rapidly upon contact with water or gastrointestinal fluids. This swelling action helps break tablets apart, promoting quick dispersion and dissolution, which leads to faster onset of the tablets intended action.
Q: What are the specific quality standards for Croscarmellose Sodium?
A: It must meet key pharmaceutical standards: loss on drying not exceeding 10%, pH between 5.0 and 7.0 (for a 1% solution), bulk density of 0.450.55 g/cm, purity above 98%, heavy metals below 10 ppm, and strict microbial limits. Residue on ignition should be between 8.010.0% and most particles (85%) pass through an 80 mesh sieve.
Q: Where is Croscarmellose Sodium commonly applied?
A: Its primary application is in pharmaceutical tablet and capsule manufacturing as a superdisintegrant. However, it also finds use in nutraceutical and food industries due to its safety, functionality, and compliance with relevant quality standards.
Q: What is the recommended process for storing Croscarmellose Sodium?
A: It should be stored in a cool, dry place away from moisture and direct sunlight to preserve its physical and chemical properties. When stored properly, Croscarmellose Sodium maintains its efficiency and safety profile for up to 36 months.
Q: When should Croscarmellose Sodium be used in tablet formulations?
A: It is best used when rapid tablet disintegration and immediate drug release are desired. This is essential for formulations where a fast onset of action is of therapeutic importance.
Q: What are the benefits of choosing pharma-grade Croscarmellose Sodium?
A: Pharma-grade Croscarmellose Sodium ensures consistency in performance, meets international safety and quality benchmarks, and reduces risks of contaminationcrucial for regulated industries like pharmaceuticals and nutraceuticals.