Pharmaceutical-grade ethyl cellulose meeting USP/NF, EP, and JP monograph requirements for excipients.
Controlled ethoxy substitution (44–48% ethoxy content) ensuring consistent film-forming and release-modifying performance.
Low viscosity grade (14 mPa·s in 5% w/w toluene/ethanol 4:1 solution at 25°C) enabling easy processing in coating and granulation operations.
Non-ionic, water-insoluble polymer with excellent organic solvent solubility (e.g., ethanol, acetone, dichloromethane).
Stable under typical pharmaceutical manufacturing conditions and compatible with common APIs and excipients.
Sustained-release oral solid dosage forms (e.g., matrix tablets, multiparticulates).
Functional film coatings for controlled drug release and moisture barrier protection.
Binders in wet granulation and dry granulation processes for low-dose or sensitive APIs.
Matrix-forming agent in implantable or biodegradable delivery systems.
| Chemical Type | Ethyl cellulose ether derivative |
| Product Form | White to off-white free-flowing powder |
| Appearance | Free-flowing granular or powdery solid |
| Primary Applications | Pharmaceutical sustained-release matrices and functional coatings |
| Key Features | USP/NF, EP, and JP compliant; low viscosity; organic-soluble; non-ionic |
| Storage Conditions | Store in a cool, dry place below 30°C in original sealed container |
| Shelf Life | 36 months from date of manufacture when stored as recommended |
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