Highly uniform particle size distribution for consistent flow and compression behavior.
Optimized crystallinity and surface morphology to enhance tablet tensile strength and disintegration performance.
Low moisture content (<5.0%) ensuring excellent stability during storage and processing.
Free-flowing powder with low dust generation, improving handling safety and operational efficiency.
Pharmaceutical-grade purity compliant with USP/NF, EP, and JP monographs for excipients.
Direct compression tablet formulation in oral solid dosage forms.
Binder and filler in chewable and rapidly disintegrating tablets.
Stabilizer and bulking agent in lyophilized biopharmaceutical formulations.
Excipient in veterinary pharmaceutical tablets and capsules.
Carrier in dry powder inhaler (DPI) formulations requiring high aerosolization efficiency.
| Chemical Type | Microcrystalline cellulose (MCC) |
| Product Form | Free-flowing white powder |
| Appearance | White to off-white, odorless, tasteless powder |
| Primary Applications | Pharmaceutical direct compression, binder, disintegrant, stabilizer |
| Key Features | Controlled particle size, high compressibility, low moisture, low endotoxin |
| Compliance | USP/NF, EP 10.0, JP 17, ISO 9001 certified manufacturing |
| Particle Size (D50) | 100–120 µm (laser diffraction) |
| Loss on Drying (LOD) | ≤4.5% (105°C, 2 h) |
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E-mail: wangxingqiang@ericwchem.com
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Building A1, Jiete Industrial Park, Huangpu District, Guangzhou City, Guangdong Province, China