Pharmaceutical-grade ethyl cellulose meeting USP/NF, EP, and JP monograph requirements for excipients.
Controlled ethoxy substitution (44–50% w/w) ensuring consistent film-forming and sustained-release performance.
Low viscosity grade (10 mPa·s in 5% w/w toluene/ethanol solution at 25°C) enabling easy processing in coating and granulation.
Non-ionic, water-insoluble polymer with excellent organic solvent solubility (e.g., ethanol, acetone, dichloromethane).
Stable across pH 3–10 and compatible with common APIs and excipients in solid oral dosage forms.
Sustained-release matrix tablets and multiparticulate systems (e.g., pellets, beads).
Functional film coatings for controlled drug release and taste masking.
Binders in direct compression and dry granulation formulations.
Viscosity modifiers in topical gels and ophthalmic suspensions.
Encapsulation aids in hot-melt extrusion and spray congealing processes.
| Chemical Type | Non-ionic ethyl ether of cellulose |
| Product Form | White to off-white free-flowing powder |
| Appearance | Odorless, tasteless, fine particulate powder |
| Primary Applications | Oral sustained-release dosage forms, film coatings, binders |
| Key Features | USP/NF, EP, JP compliant; low viscosity; high purity |
| Storage Conditions | Store in original sealed container at 15–25°C, <60% RH |
| Solubility Profile | Soluble in ethanol, acetone, chloroform, toluene; insoluble in water |
| Microbial Limits | Complies with USP <61>: Total aerobic microbial count ≤100 CFU/g |
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