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Pharmaceutical-grade methylcellulose meeting USP/NF, EP, and JP monograph requirements.
Controlled viscosity profile (400–600 mPa·s in 2% aqueous solution at 20°C) for consistent formulation performance.
Excellent cold-water solubility with rapid dispersion and minimal lump formation.
High purity with low residual methanol and heavy metals—optimized for oral solid dosage forms.
Thermally reversible gelation behavior enabling use in hot-melt extrusion and sustained-release matrix systems.
Matrix-forming polymer in immediate-release and modified-release tablets.
Viscosity-enhancing agent in liquid and semi-solid oral suspensions and syrups.
Binder in direct compression and wet granulation processes.
Coating component for functional film coatings in tablet and capsule applications.
Stabilizer and thickener in ophthalmic solutions and nasal sprays.
| Chemical Type | Methylcellulose ether (non-ionic cellulose derivative) |
| Product Form | White to off-white free-flowing powder |
| Appearance | Odorless, tasteless, fine granular powder |
| Primary Applications | Oral solid dosage forms, liquid formulations, topical preparations |
| Key Features | USP/NF, EP, JP compliant; low endotoxin; suitable for GMP manufacturing |
| Benefits | Batch-to-batch consistency, high reproducibility in compaction and dissolution, regulatory support documentation available |
| pH of 1% Aqueous Solution | 5.0–8.0 |
| Loss on Drying | ≤8.0% (at 105°C for 2 hours) |
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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
