Highly uniform particle size distribution for consistent flow and compression behavior in direct compression tablet formulations.
Optimized crystallinity and surface morphology to enhance binding efficiency and tablet hardness without excessive binder load.
Low moisture content (≤5.0%) ensuring excellent stability during storage and compatibility with moisture-sensitive APIs.
Free-flowing, non-dusting powder with high bulk density (~0.35–0.45 g/cm³) facilitating accurate dosing in high-speed tablet presses.
Pharmaceutical-grade purity compliant with USP/NF, EP, and JP monographs for microcrystalline cellulose.
Direct compression excipient in oral solid dosage forms, including immediate-release tablets and chewables.
Binder and filler in low-dose potent drug formulations requiring high dilution capacity and content uniformity.
Stabilizer and bulking agent in lyophilized biopharmaceutical formulations and diagnostic reagent tablets.
Carrier matrix in dry powder inhalers (DPIs) due to its favorable aerosolization performance and low electrostatic charge.
| Chemical Type | Microcrystalline cellulose (MCC) |
| Product Form | Free-flowing white to off-white granular powder |
| Appearance | White or almost white, odorless, tasteless powder |
| Primary Applications | Direct compression tablet excipient, binder, filler, disintegrant aid |
| Key Features | High compressibility, excellent flowability, low moisture sensitivity |
| Compliance | USP/NF, Ph. Eur., JP, and FDA GRAS listed |
| Residue on Ignition | ≤0.3% |
| Heavy Metals (as Pb) | ≤10 ppm |
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E-mail: wangxingqiang@ericwchem.com
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