Highly uniform particle size distribution for consistent flow and compression behavior in direct compression tablet formulations.
Optimized crystallinity and surface area to enhance binding efficiency and tablet hardness without excessive binder load.
Low moisture content (< 5.0%) ensuring excellent chemical stability and reduced risk of hydrolysis in moisture-sensitive APIs.
Free-flowing, non-hygroscopic powder with low dust generation—ideal for high-speed capsule fillers and tablet presses.
Complies with major pharmacopoeial standards including USP-NF, EP, and JP for pharmaceutical excipient use.
Direct compression tablet formulation for oral solid dosage forms, especially for low-dose potent APIs.
Filler-binder in chewable tablets requiring rapid disintegration and smooth mouthfeel.
Stabilizer and bulking agent in lyophilized biopharmaceutical formulations.
Excipient in veterinary pharmaceutical tablets and medicated feed premixes.
Carrier matrix in dry powder inhalers (DPIs) due to its aerodynamic particle characteristics.
| Chemical Type | Microcrystalline cellulose (MCC) |
| Product Form | Free-flowing white to off-white granular powder |
| Appearance | White, odorless, tasteless, fine granules |
| Primary Applications | Pharmaceutical direct compression, wet granulation, and stabilization |
| Key Features | Uniform particle size, low moisture, high compressibility, excellent flowability |
| Compliance | USP-NF, Ph. Eur., JP, and FDA GRAS status |
| Residue on Ignition | ≤ 0.3% |
| Heavy Metals (as Pb) | ≤ 10 ppm |
Contact With Us:
E-mail: wangxingqiang@ericwchem.com
Have a Questions? Call Us:
Add:
Building A1, Jiete Industrial Park, Huangpu District, Guangzhou City, Guangdong Province, China