Pharmaceutical-grade purity compliant with USP/NF, EP, and JP monographs for oral solid dosage forms.
Consistent viscosity performance (4–6 mPa·s in 2% aqueous solution at 20°C) ensuring reliable tablet binder functionality.
Excellent cold-water solubility with rapid hydration and minimal claying, enabling efficient wet granulation processes.
Non-ionic, pH-independent behavior across physiological ranges (pH 3–11), supporting formulation stability in diverse APIs.
Low endotoxin levels (<0.5 EU/mg) and stringent microbial control meeting ICH Q5D and compendial requirements for sterile and non-sterile products.
Primary binder in direct compression and wet granulation of immediate-release tablets.
Controlled-release matrix former in hydrophilic polymer-based extended-release tablets.
Viscosity enhancer and suspending agent in oral liquid suspensions and syrups.
Protective colloid and film-forming agent in pharmaceutical coating formulations.
Excipient in lyophilized formulations and ophthalmic solutions requiring low osmolality and high clarity.
| Chemical Type | Methylcellulose ether (non-ionic cellulose derivative) |
| Product Form | White to off-white free-flowing powder |
| Appearance | Fine, odorless, tasteless powder |
| Viscosity (2% w/w aqueous solution, 20°C) | 4–6 mPa·s |
| Methoxy Substitution (USP/NF) | 27.0–30.0% |
| Loss on Drying (105°C, 2 h) | ≤5.0% |
| Residue on Ignition | ≤1.5% |
| Microbial Limits (USP <61>) | Total aerobic count ≤100 CFU/g; absence of E. coli, Salmonella, and S. aureus |
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